Medical Director - Clinical Oncology
Posted 5 days ago
Job Viewed
Job Description
**Job Description**
**_Objective / Purpose:_**
+ **_Lead and strengthen OTAU R&D capabilities in India_** _to maximize the value for accelerating global innovation and efficiency, in alignment with global OTAU R&D goals._
+ **_Ensure effective oncology operations in India_** _by leveraging local opportunities and overseeing all OTAU Clinical Science activities in India. Be accountable for speed and quality in collaboration with the global OTAU team and if appropriate OTAU-China, OTAU-Japan and other global R&D functions._
+ **_Partner with ISEA and India LOC leaders_** _to enhance enterprise-level efforts for accelerating global clinical trials._
**_Accountabilities:_**
**Lead India R&D Strategy and Execution**
+ Work closely with OTAU GPTs a and Global R&D functions to optimize integrated India development strategy for pipeline assets
+ Monitor overall country performance and support country focused oncology activities e.g. feasibility and site selections to deliver country operational milestones
+ Serve as the internal expert on India's clinical development to inform global development strategy. Collaborate closely with India LOC to execute One Oncology strategy in India including tapping into local expertise and community networks
+ Collaborate and work closely with Oncology GPTs, the Global R&D team and regional teams, as appropriate, for each asset or indications under the remit
+ Engage study investigators to maintain strong interest and focus on Takeda's oncology clinical trials
+ Proactively build and maintain strong investigator networks in India to support current and future trials across Takeda's oncology portfolio in both solid tumors and hematologic malignancies and proactively share with the OTAU and Global teams
+ Build and scale global clinical trial capabilities in India as a key market in collaboration with LOC, Region and Global teams to accelerate Takeda innovation and boost efficiency
**Clinical Development team participation and leadership**
+ Leads the Development Team in India for assigned compounds. In some cases may lead clinical directors or clinical scientist(s) responsible for leading this team with an emphasis on proactively identifying contingencies, risks, and mitigation strategies.
+ Directs Development Team strategy and deliverables overseeing the Development Strategy, Clinical Development Plan and Clinical Protocols in India. Recommends scope, complexity and size, which influence the budget of all aspects of a program. Provides continual critical and constructive evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them.
+ Responsible for high impact India specific decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development such as "go/no go" decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical significance considering how a given product will fit in with current treatments, standard of care, and unmet medical need.
**C. Synopsis / Protocol Development, Study Execution, & Study Interpretation**
+ _Leads Oncology Clinical Science activities in India, including protocol development, study execution, and data interpretation._
+ _Serves as an advisor to the clinical scientists involved in these activities, and be accountable to senior company management for the successful completion of underlying objectives. For the assigned compounds, accountable for the successful completion of projects undertaken - and for pro-active contingency planning / interventions necessary to ensure achievement of related goals._
+ _Interprets data from an overall scientific standpoint as well as within the context of the medical significance to individual patients._
**Trial Medical Monitoring**
+ _Oversees medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses overall safety information for studies and compounds in conjunction with_ _Pharmacovigilance._
**External Interactions**
+ _Leads KOL and investigator engagement strategies to support development of assigned compounds, and contributes to regulatory strategy in India_
+ _Provides leadership and serves as an advisor to the other clinical physicians and scientists engaged in these activities and, in the context of these responsibilities, will be accountable to senior leadership for the successful completion of related objectives in India._
**Due Diligence, Business Development and Alliance Projects**
+ _Can be assigned to be responsible for identification and evaluation of potential business development opportunities, conducts due diligence evaluations, and development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities, as assigned. As part of a global due diligence team, assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with BD teams_
+ _As assigned, serves as clinical point of contact for ongoing alliance projects and interfaces with partner to achieve Takeda's strategic goals while striving to maintain good working relationship between Takeda and partner. Provides guidance to clinical scientists who are involved in some of these activities._
**Leadership, Task Force Participation, Upper Management Accountability**
+ _Interacts directly with research division based on pertinent clinical and development expertise and with NPP to provide_ _knowledge/understanding_ _of India market environment. Represents clinical science on high impact/priority task forces across the organization or external to the company._
+ _While currently an individual contributor position, the position may evolve or progress to be responsible in hiring, managing, mentoring, motivating, empowering, developing and retaining staff members to support assigned activities. Drives performance management, career development, and team engagement_
**Lead** **India** **Oncology Clinical Science team**
+ _Build, manage/overs_ _ee_ _and engage the_ _OTAU members in India_
+ _Foster a high-performing team culture with a focus on development, well-being, and alignment with OTAU's mission_
**Serving as Country Matter Expert**
+ _Be a strong advocate for the Takeda ONE Oncology and R&D organizations in_ _India_ _in collaboration with_ _India_ _LOC; serve as local bridge for any future opportunities in engaging_ _India_ _innovation ecosystem_
+ _Point for escalation for resolution of complex country related issues & risk and serve as a site escalation point for oncology investigator concerns_
+ **Lead and develop oncology clinical strategies for India according to business needs as assigned**
**_Education & Competencies:_**
**Education, Experience, Knowledge and Skills:**
+ _MD, combined MD/PhD or internationally recognized equivalent_
+ _Clinical Training in Malignant Hematology and/or Medical Oncology preferred_
+ _Minimum 3 to 5 years of clinical research experience in the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned)._
+ _Minimum of 4 to 5 years of people management experience in a healthcare or life sciences setting is preferred._
+ _Proven success in leading global or regional clinical development teams, including responsibility for multi-regional studies. Experience beyond US/EU is a plus._
+ _Experience with NDA/MAA Submission preferred_
+ _Experience and expertise in clinical trial management and support of marketing authorization in India as required._
+ _Demonstrated ability to lead and manage cross-functional medical, scientific and technical teams_
**Skills**
+ _Superior communication, strategic, interpersonal and negotiating skills_
+ _Ability to anticipate challenges and drive proactive problem-solving_
+ _Ability to drive decision-making within matrixed multi-regional teams_
+ _Diplomacy and positive influencing abilities across diverse cultures_
+ _Solid teamwork, organizational, interpersonal, and problem-solving skills; exercises good judgment with respect to Takeda confidential information and strategies_
+ _Fluent business English (oral and written) and strong medical writing capabilities_
**Knowledge**
+ _Deep understanding of oncology therapeutic areas, including mechanisms of action relevant to assigned compounds._
+ _Strong knowledge of global regulatory and compliance requirements, including but not limited to ICH GCP; awareness of local country requirements is essential._
+ _Familiarity with emerging research trends in designated therapeutic area_
**TRAVEL REQUIREMENTS:**
+ _Ability to drive to or fly to various meetings or client sites, including overnight trips. Some international travel may be required._
+ _Requires approximately 15 - 25% travel._
**Locations**
Mumbai, India
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
Medical Director - Clinical Oncology
Posted today
Job Viewed
Job Description
Description
Lead India R&D Strategy and Execution
Clinical Development team participation and leadership
C. Synopsis / Protocol Development, Study Execution, & Study Interpretation
Trial Medical Monitoring
External Interactions
Due Diligence, Business Development and Alliance Projects
Leadership, Task Force Participation, Upper Management Accountability
Lead India Oncology Clinical Science team
Serving as Country Matter Expert
Education, Experience, Knowledge and Skills:
Skills
Knowledge
TRAVEL REQUIREMENTS:
Locations
Mumbai, IndiaWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeMedical Science Liaison, Oncology
Posted 6 days ago
Job Viewed
Job Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Medical Science Liaison, Oncology
Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to Abbvie initiatives in assigned therapeutic areas.
Executes against the Medical Affairs plan for India. Provides scientific education and training initiatives across Abbvie Oncology portfolio. Plans and leads scientific communication with key therapy leaders and stakeholders, organizing advisory board meetings, facilitating clinical trials, and serving as the medical resource for both external and internal stakeholders. This position is a non-promotional role. The primary focus is providing Healthcare Professionals with fair and balanced scientific information.
Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by Abbvie. Works closely with other Abbvie personnel to ensure information, education, and research needs of healthcare professionals are met and to ensure scientific and technical training needs of commercial organizations are identified and met.
Key Responsibilities Area
As an internal medical / technical / scientific resource, leads medical affairs objectives in the affiliate country. The role requires competency in practical aspects of patient care, and the ability to use medical and scientific information to facilitate engagement of physicians and others in the clinical and basic scientific issues relevant to Abbvie's products.
Responsible for maintaining annual expenses within assigned budget parameters.
Responsible for accurate and timely documentation of medical lead activities.
The employee must conduct their work activities in compliance with all Abbvie internal requirements and with all applicable regulatory requirements. Abbvie internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives.
Identify, develop and maintain professional relationships with thought leaders, academic centers and researchers in assigned areas of therapeutic interest to ensure access to current medical and scientific information on Abbvie products.
Work closely with the Commercial leaders for business planning , Therapeutic leads & Dir, Medical Affairs to set priorities, and activities.
Upon request, present data on Abbvie products to healthcare professionals including physicians, academic institutions, researchers, and other health care professionals.
Support research initiatives as requested by Abbvie R&D, Clinical Operations, and Medical Affairs Departments.
Serve as internal medical and scientific resource to assigned Abbvie therapeutic areas for development of disease-state and product communications and materials that are medically accurate, balanced, and consistent with regulatory guidelines.
Support Round Table and Advisory Board sessions to ensure accuracy of scientific and clinical data.
Conducts on-going training to medical affairs, field sales and other internal personnel as required.
A high level of travel / field time is to be expected within this position (approximately 60% of time spent outside the office). This role will also serve as the local representative of the Global Medical Office associated functions. (eg PV, HEOR etc)
Qualifications
Qualifications
Requirements
Minimum 2-3 years post-qualification work experience in Medical affairs function.
Experience working within the pharmaceutical industry or within clinical research is preferred
Experience of working collaboratively and cross-functionally in a matrix structure, supporting multiple stakeholders
Demonstrated ability to learn quickly and convey clinical and non-clinical technical information effectively to individuals with varying degrees of scientific acumen.
Demonstrated strong presentation and teaching skills with ability to effectively share information with others
Demonstrated ability to develop and maintain strong relationships; to lead & engage
Experience applying analytical skills, to critically evaluate and effectively communicate key clinical data
Experience working with technology, including systems such as Microsoft Office.
Education
MD;
MBBS
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Opportunity for Oncology Nurse
Posted today
Job Viewed
Job Description
Company Overview
Sir H. N. Reliance Foundation Hospital and Research Centre, based in Mumbai, is a premier 345-bed multi-speciality tertiary care institution known for its cutting-edge technology and advanced medical care. The hospital excels in areas like Oncology, Cardiac Sciences, and Neuro Sciences among others. With a history dating back to 1918 and a focus on respect for life, Sir H.N. Reliance Foundation Hospital is renowned for its international standards in infrastructure and patient care.
Job Overview
The Oncology Nurse position at Sir H.N. Reliance Foundation Hospital & Research Centre is a full-time role located in Mumbai. As part of the Oncology department, the nurse will provide compassionate care to cancer patients, assist in the administration of radio and chemotherapy treatments, and collaborate closely with a skilled team of healthcare professionals. This role demands both technical expertise and empathy to support patients through their treatment journey.
Qualifications and Skills
- Completion of a recognized nursing program with valid nursing licensure.
- Proficiency in administering chemotherapy and radiation therapy to cancer patients.
- Strong assessment skills for monitoring patient status and managing side effects.
- Exceptional communication abilities to educate patients and families on treatment processes.
- Experience in developing individualized care plans in collaboration with an interdisciplinary team.
- Ability to handle emotional situations and provide psychological support to patients and families.
- Strong organizational skills for maintaining accurate medical records and documentation.
- Commitment to continuous learning and improvement in the oncology nursing field.
Roles and Responsibilities
- Administer chemotherapy and radiation therapy as prescribed by the oncologists.
- Monitor patients during treatment and manage any immediate side effects.
- Coordinate with the oncology team to deliver comprehensive care plans.
- Educate patients and their families about treatment plans and potential side effects.
- Maintain meticulous records of patient treatments and progress.
- Support patients emotionally, addressing concerns and providing reassurance.
- Participate in ongoing training to enhance skills and knowledge in oncology care.
- Ensure adherence to hospital policies, safety guidelines, and ethical standards at all times.
Nurse Manager – Oncology Daycare
Posted today
Job Viewed
Job Description
Dear Candidate,
Greetings!
Sir H. N. Reliance Foundation Hospital and Research Centre is a state-of-the-art 345 bed multi-specialty tertiary care hospital, situated in South Mumbai, committed to make world class healthcare accessible to all.
We currently have openings for Nurse Manager Oncology Daycare , details for the same are given below
Candidates Requirement: -
15+ years of nursing experience out of which minimum 5 years as a manger /supervisor
M. Sc. / B.Sc. Degree in Nursing from a recognized nursing institute.
Additional hospital administration courses for diploma nurses.
Should have nursing council registration
Job Profile: -
Responsible to deliver a professional, safe and quality patient care through the nursing process of assessment, planning, implementation and evaluation.
Responsible for effective communication with patients, relatives and members of the health care team.
Help to meet the psychological, emotional and informational needs of cancer patients at the time of diagnosis, and throughout treatment. The support will be provided in the following areas:
Inpatient oncology unit
Oncology Day Unit
Throughout the hospital to patients who are referred to the Oncology Service via a consultant.
Responsible for safe and quality patient care during diagnostic and minimally invasive, image-guided procedures used to treat the patient.
Plan, organize, direct and control all department operations including routine and emergency nursing care, academics, inter and intra departmental collaborations, people management, infrastructure and other administrative functions
Manage/supervise/assist ward managers through facilitation, time management and problem solving
Adhere to all clinical and nursing protocol as per Hospital Policies of Sir H N Reliance Foundation
In case, you are interested kindly send your updated profile on and , along with the following details:
- Contact details:
- Current CTC:
- Notice period:
You can refer this mail to your friends/colleagues. To know more about our hospital, please visit
Regards,
Human Resources,
Sir H. N. Reliance Foundation Hospital and Research Centre
Statistics Leader - Oncology Statistics
Posted today
Job Viewed
Job Description
Join our industry-leading Statistics team, dedicated to embedding high-quality quantitative reasoning at the heart of every project in our portfolio. At GSK, statisticians are essential in maximizing the use of all available data points to efficiently develop translational strategies that underpin our comprehensive clinical development plans.
The Oncology Clinical Development Statistics group is seeking exceptionally talented and dedicated Statisticians. In this role, you will apply your statistical expertise and innovative methodologies to make key contributions to the development of new medicines in the Oncology field. You will provide statistical and strategic insights into clinical development plans and the design of end-to-end development strategies, from early first-in-human trials to late-phase drug development. Our team is committed to utilizing novel clinical trial designs and innovative statistical methods, including Bayesian techniques, to assess risk as well as probability of success for both studies and overall programs to enable informed decision-making.
Despite the listing of GSK-Upper Providence as the primary job location, candidates will be considered equally from the Upper Providence (USA), Waltham (USA), GSK HQ – London (UK) and Stevenage (UK) sites. 2-3 days per week on site.
Key Responsibilities:
Provide required statistical support to Project and Study Statisticians across the oncology team
Provide statistical input to the design, analysis, reporting and interpretation of clinical studies using a wide range of statistical approaches and/or applicable software (e.g. simulation, Bayesian methods, interim analysis strategies), while influencing clinical development, regulatory, and commercial strategies.
Author statistical analysis plans and prepare statistical input to key documents (including protocol) and presentation material, while collaborating with internal and external partners to meet business needs
Apply standard processes to tasks to ensure that deliverables are accurate, high quality and meet agreed timelines
Build and maintain effective strategic working relationships with internal and external partners to meet business needs
Identify, develop, and implement novel statistical methodologies in support of medicines development and formulate data strategies to leverage internal and external databases for R&D oncology and invest in expanding expertise across clinical, regulatory, and commercial domains.
Why you?
Basic Qualifications:
MS in Statistics or related discipline with 5+ years of relevant experience
Experience in clinical research (Pharma, CRO, or academic setting)
Experience in late phase drug development
Experience implementing innovative method by simulation using R, SAS or other software
Preferred Qualifications:
PhD in Statistics or closely related field (+3 years' experience in Oncology)
Practical understanding of Statistical Modelling and experience with Bayesian methods
Expertise and practical application in multiple statistical methodologies & innovative statistical thinking
Track record of strong performance in an industry or academic setting
Capability in building and maintaining strong working relationships in a team setting
Excellent interpersonal and communication skills & demonstrated ability to explain novel and standard methods to scientific and clinical colleagues
Demonstrated ability to lead or make major contributions to department, organizational and/or industry-wide initiatives, through effective communication and influence.
Proficient in both spoken and written communication, with the capability to clearly communicate both new and established statistical methods and results peers without substantial statistical training
Self-motivated and independent worker
Strong time management skills; able to effectively organize and manage a variety of tasks across different projects
Please visit to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.
Production Supervisor (Oncology Osd)
Posted today
Job Viewed
Job Description
- Position Purpose:
- The Supervisor is responsible for managing his team to carry out the manufacturing operations according to schedule in compliance with HSE and GMP rules. Coordinate production staff, employee rotation and employee movement, evaluate employee performance, ensure compliance with collective agreements, policies and legislation. Assign work according to production needs, review, approves and draft documents relevant to management of production activities, issues, recommendations on production organization and makes adjustment. Ensure supply of raw materials, components and other products for production, check equipment availability and operational status, ensure production process are carried out, ensure workplace safety and proper management of waste and residual material. Ensure supply of raw materials, components and other products for production, check equipment availability and operational status, ensure production process are carried out, ensure workplace safety and proper management of waste and residual material.
- Your key responsibilities:
- Your responsibilities include, but are not limited to:
- Represent production management to the team members and promote Novartis values within the team. Line responsibility and shift walkthrough. Engage and motivate the team and delivers strong results with an empowered team. Provide front line expert support for all process-specific issues to production. Act as Subject Matter Expert (SME) for the product and process.
- Coordinate and ensure the completion of all production operations on time, in accordance with the documentation and in compliance with GMP, SSE and 5S rules Operation Scheduler. Is responsible to provide a feasible plan to the shop floor in terms of materials and capacity availability.
- Establish optimized sequence of orders within the Planning Time Fence and keep it up to date, based on rules agreed by manufacturing, Quality and other support functions and in accordance with Customer requirements. Provide the planning status in the daily production meeting.
- Manufacturing Systems Expert, Define User requirement specifications (Voice of customer) Design and create electronic batch files (EBR) with respect for quality, costs and deadlines. MBR / BOM/ Recipe creation in production IT systems
- Participate in the qualification and risk assessment processes, delivers engaging technical training programs, using multiple delivery methodologies (OJT, Classroom, virtual classroom etc.) to support qualification of associates to perform technical tasks and develop technical capabilities. Present site training strategy and respond to auditor questions
- Promote and improve the HSE culture, by implementing the necessary systems and actions in line with the evolution of the site. Promote and improve the Quality culture in collaboration with Quality Assurance and ensure overall inspection readiness for area of responsibility.
- Weekly, Monthly production planning and preparing daily and all monthly production reports and to full fill monthly targets. Tackle technical problems during manufacturing of products. Documentation of change control, deviations, discrepancies and market complaints investigation if any.
**Commitment to Diversity & Inclusion**:
- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Minimum requirements**
- What you’ll bring to the role:
- B. Pharm / M. Pharm, Preferably MBA in Operations
- Experience in OSD Oncology Manufacturing in reputed pharma company.
- Minimum 5 years’ experience in supervisory / frontline manager capacity.
Commitment to Diversity & Inclusion:
- Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.- Why Sandoz?
- 500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world.
- How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
- We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
- Imagine what you could do here at Sandoz!
**Division**
- Novartis Technical Operations
**Business Unit**
- NTO SANDOZ TECH
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About the latest Oncology Jobs in Mumbai !
Opportunity for Oncology Nurse
Posted 9 days ago
Job Viewed
Job Description
Company Overview
Sir H. N. Reliance Foundation Hospital and Research Centre, based in Mumbai, is a premier 345-bed multi-speciality tertiary care institution known for its cutting-edge technology and advanced medical care. The hospital excels in areas like Oncology, Cardiac Sciences, and Neuro Sciences among others. With a history dating back to 1918 and a focus on respect for life, Sir H.N. Reliance Foundation Hospital is renowned for its international standards in infrastructure and patient care.
Job Overview
The Oncology Nurse position at Sir H.N. Reliance Foundation Hospital & Research Centre is a full-time role located in Mumbai. As part of the Oncology department, the nurse will provide compassionate care to cancer patients, assist in the administration of radio and chemotherapy treatments, and collaborate closely with a skilled team of healthcare professionals. This role demands both technical expertise and empathy to support patients through their treatment journey.
Qualifications and Skills
- Completion of a recognized nursing program with valid nursing licensure.
- Proficiency in administering chemotherapy and radiation therapy to cancer patients.
- Strong assessment skills for monitoring patient status and managing side effects.
- Exceptional communication abilities to educate patients and families on treatment processes.
- Experience in developing individualized care plans in collaboration with an interdisciplinary team.
- Ability to handle emotional situations and provide psychological support to patients and families.
- Strong organizational skills for maintaining accurate medical records and documentation.
- Commitment to continuous learning and improvement in the oncology nursing field.
Roles and Responsibilities
- Administer chemotherapy and radiation therapy as prescribed by the oncologists.
- Monitor patients during treatment and manage any immediate side effects.
- Coordinate with the oncology team to deliver comprehensive care plans.
- Educate patients and their families about treatment plans and potential side effects.
- Maintain meticulous records of patient treatments and progress.
- Support patients emotionally, addressing concerns and providing reassurance.
- Participate in ongoing training to enhance skills and knowledge in oncology care.
- Ensure adherence to hospital policies, safety guidelines, and ethical standards at all times.
Nurse Manager – Oncology Daycare
Posted 21 days ago
Job Viewed
Job Description
Dear Candidate,
Greetings!
Sir H. N. Reliance Foundation Hospital and Research Centre is a state-of-the-art 345 bed multi-specialty tertiary care hospital, situated in South Mumbai, committed to make world class healthcare accessible to all.
We currently have openings for Nurse Manager Oncology Daycare , details for the same are given below
Candidates Requirement: -
15+ years of nursing experience out of which minimum 5 years as a manger /supervisor
M. Sc. / B.Sc. Degree in Nursing from a recognized nursing institute.
Additional hospital administration courses for diploma nurses.
Should have nursing council registration
Job Profile: -
Responsible to deliver a professional, safe and quality patient care through the nursing process of assessment, planning, implementation and evaluation.
Responsible for effective communication with patients, relatives and members of the health care team.
Help to meet the psychological, emotional and informational needs of cancer patients at the time of diagnosis, and throughout treatment. The support will be provided in the following areas:
Inpatient oncology unit
Oncology Day Unit
Throughout the hospital to patients who are referred to the Oncology Service via a consultant.
Responsible for safe and quality patient care during diagnostic and minimally invasive, image-guided procedures used to treat the patient.
Plan, organize, direct and control all department operations including routine and emergency nursing care, academics, inter and intra departmental collaborations, people management, infrastructure and other administrative functions
Manage/supervise/assist ward managers through facilitation, time management and problem solving
Adhere to all clinical and nursing protocol as per Hospital Policies of Sir H N Reliance Foundation
In case, you are interested kindly send your updated profile on and , along with the following details:
- Contact details:
- Current CTC:
- Notice period:
You can refer this mail to your friends/colleagues. To know more about our hospital, please visit
Regards,
Human Resources,
Sir H. N. Reliance Foundation Hospital and Research Centre
Medical Science Liaison - Oncology -Central
Posted today
Job Viewed
Job Description
Sun Pharma is the world’s fourth largest specialty generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology.
Job Summary:
The MSL will primarily identify and engage with a targeted group of national and regional thought leaders/healthcare professionals (HCPs) as well as payers and managed care accounts, providing the consistent delivery of educational and compliant scientific information in support of Oncology products. The MSLs will engage with HCPs, NPs, & PAs who are in clinical practice caring for their patients. They will be trained to respond to complex inquiries in a scientific, fair-balanced, compliant manner serving as a critical field medical resource to these HCPs and also, internal SUN sales and managed markets constituents.
Responsibilities:
Qualifications:
The presently-anticipated base compensation pay range for this position is $, to $,. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; (k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives:
Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.