19 Medical Oncology jobs in India

Lead Medical Researcher (Oncology)

226001 Lucknow, Uttar Pradesh ₹1400000 Annually WhatJobs

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full-time
Our client, a world-renowned research institution, is seeking an accomplished Lead Medical Researcher specializing in Oncology to spearhead groundbreaking studies. This fully remote position offers a unique opportunity to drive innovation in cancer research from your home laboratory or dedicated workspace. You will lead a team of scientists, manage research projects from conception to completion, and contribute significantly to the scientific community through publications and presentations. The ideal candidate will possess a Ph.D. or M.D. in a relevant life science field, a strong publication record, and extensive experience in oncology research, including preclinical and/or clinical trial design. Proficiency in advanced molecular biology techniques, data analysis, and interpretation is essential. Responsibilities include developing innovative research hypotheses, designing and executing experiments, securing research grants, and mentoring junior researchers. You will also collaborate with cross-disciplinary teams and external partners to advance research objectives. This remote role requires exceptional leadership qualities, meticulous scientific rigor, excellent project management skills, and the ability to work independently and effectively in a virtual environment. We are looking for a visionary scientist with a passion for discovery and a commitment to improving patient outcomes. The strategic direction of research efforts impacts advancements within the broader medical and scientific landscape, including areas surrounding Lucknow, Uttar Pradesh, IN . Expertise in specific areas of oncology, such as immunotherapy, targeted therapies, or cancer genomics, will be highly regarded. This is an exciting chance to lead pioneering research that has the potential to transform cancer treatment and patient care.
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Medical Doctor

Pune, Maharashtra ALIV - Regenerative Wellness

Posted 5 days ago

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Medical Counselor / Clinical Doctor


Location: Pune, India

Experience: 3–7 years

Employment Type: Full-time


About ALIV Regenerative Wellness


ALIV is India’s pioneer in regenerative wellness and IV infusion therapies, offering personalized protocols that combine medical precision with holistic care. Our clinics are designed to deliver premium patient experiences while setting the standard for safe, ethical, and cutting-edge therapies across the country.


Role Overview


We are looking for qualified doctors (BHMS, BAMS, MBBS) to join our Mumbai clinical team as Medical Counselors and Clinical Support Doctors . This hybrid role combines patient consultation, IV infusion oversight, emergency preparedness, and surgical assistance experience .


The ideal candidate will excel in both patient-facing counseling and hands-on clinical skills — particularly IV line setup, infusion therapy administration, and minor procedure assistance — while providing empathetic guidance to patients about their treatments.


Key Responsibilities


Patient Consultation & Counseling


  • Conduct detailed consultations, review medical histories, and ensure accurate EMR documentation.
  • Educate and counsel patients on IV protocols, regenerative therapies, and treatment plans in clear, empathetic language.
  • Address patient queries, building trust and confidence before, during, and after treatments.


Clinical & Procedural Support


  • Flawlessly set up IV lines — ensuring one-prick, pain-free insertion for every patient.
  • Oversee IV infusions and regenerative therapy administration in compliance with ALIV protocols.
  • Support physicians in minor procedures, regenerative injectables, and surgical preparation when needed.
  • Monitor patient vitals, identify early warning signs, and act quickly in emergencies.


Pre- & Post-Procedure Care


  • Ensure patients are well-prepared for procedures, with complete pre-treatment clearances and education.
  • Provide post-infusion guidance, including hydration, medication, and activity instructions.
  • Follow up on recovery progress and ensure seamless patient handover for continuing care.


Team Collaboration & Training


  • Work closely with nurses, therapists, and front desk staff to ensure smooth patient journeys.
  • Participate in skill-upgrading sessions, mock drills, and ongoing training to maintain top-tier clinical performance.


Required Qualifications


  • BHMS, BAMS, or MBBS degree with valid registration under the relevant council (MCI/State Council).
  • 3–7 years of clinical experience , with:

  • Proven hands-on expertise in IV cannulation (speed, accuracy, and patient comfort are key).
  • Exposure to ICU/critical care environments and emergency management protocols.
  • Experience assisting in surgical or procedural setups.


Desired Attributes


  • Calm, steady-handed, and precision-focused — committed to pain-free patient care .
  • Strong counseling skills, able to explain complex medical concepts simply and empathetically.
  • Proactive, collaborative approach to working with multidisciplinary teams.
  • Passion for wellness and regenerative medicine; eager to grow in a cutting-edge field.


What We Offer


  • Opportunity to shape the future of preventative and regenerative care in India .
  • Access to world-class training in IV infusion therapy and regenerative protocols.
  • Competitive salary and performance-based incentives.
  • A patient-first work culture with no night shifts and focus on quality over quantity.


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Medical Doctor

Tricog Health

Posted 5 days ago

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Position: Consultant Physician/ Non-invasive Cardiologist.


Qualification:

  • MBBS+ MD(General Medicine/Internal Medicine)
  • MBBS+ DNB(General Medicine/Internal Medicine)
  • MBBS+PGDCC/FNIC
  • Experience: 5+ years post MBBS.


Responsibilities:


  • Identify and report ECGs accurately and promptly within the TAT and extend support by guiding the Doctors/ Customers.
  • Review the patient's ECG and send the reports to hospitals/ clinics/ diagnostic centers/ nursing homes around the clock without delay to save critical patients.
  • Ensure support to healthcare professionals over the phone to report critical/ emergency cases detected.
  • Review the necessary information to determine the readiness of patients’ reports.
  • Ensure a detailed approach, accuracy, and timely completion of the diagnosis of ECG data.


Other Information:

Location: Remote

Position: Part-time (4-hour continuous fixed shift from 10 AM to 2PM Or 11AM TO 3 PM , with rotational offs)

Open to: Male / Female candidates

Compensation: Best in the market (based on experience)


About Tricog :

Heart disease is the leading cause of death. Much of this is preventable with good technology to detect, cure, and manage the case. At Tricog, each day we aim to achieve the same by building not just products but the ecosystems for cardiovascular disease management. We are helping patients to get access to better diagnosis and better care, potentially saving their lives, and that is what motivates us. Our team works across the entire range ,including hardware, algorithms, software, and medical expertise, to solve this pressing problem.


Our aim is to change the 80% chance that a heart attack will take your life to an 80% chance that you will survive. We use technology to help patients gain access to quick, accurate, and affordable diagnoses, which can lead to significant mortality reduction.


Meet our founding team: Tricog was founded in January 2015 by Dr. Charit Bhograj, an Interventional cardiologist by training, Dr. Zainul Charbiwala, an electrical engineer and researcher by training, and Dr. Udayan Dasgupta, an algorithms expert.

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Medical Doctor

Pune, Maharashtra The HIRD

Posted 5 days ago

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Job Title: Medical Reviewer / Medical Quality Reviewer

Location: Pune | NCR | Kolkata

Working Model: Hybrid


Qualifications:


  • MBBS (Medical Degree), preferably with a postgraduate qualification.
  • Minimum 2+ years of experience in clinical practice or pharmacovigilance (PV).
  • Must hold valid Medical Doctor certification/licensure in the country of service.
  • Experience in the pharmaceutical industry preferred.
  • Working knowledge of international regulations and guidance documents related to worldwide reporting requirements (US/EU).


Key Responsibilities:


  • Perform comprehensive medical review of cases, ensuring consistency and accuracy of information.
  • Provide causality assessment and clinical evaluation comments as required.
  • Support the preparation of clinical trial safety assessments , regulatory submissions , and aggregate safety reports .
  • Ensure compliance with pharmacovigilance regulations and company policies.
  • Identify and resolve issues independently; escalate complex matters appropriately.
  • Demonstrate strong analytical and decision-making skills in both routine and complex scenarios.
  • Collaborate effectively within a matrix organization , working both independently and under supervision.
  • Maintain high productivity, organization, and time management to meet regulatory compliance goals.
  • Exhibit excellent oral and written communication in English.


Skills & Competencies

  • Strong understanding of pharmacovigilance processes and safety data management .
  • Proficiency in database management systems and computer applications.
  • Excellent organizational and problem-solving skills.
  • Ability to work under tight timelines while maintaining quality standards.
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Medical Doctor

Maharashtra, Maharashtra Caps and Pays Executive Search

Posted 5 days ago

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Looking for Doctors !


Education: MBBS, BAMS, BHMS, BUMS

Experience: 2 to 10 yrs

Location: Maharashtra


Company : Emergency Medical Services.

Looking for Doctors who are passionate about serving people in distress, and emergency.


Should be able to handle the Emergency Medical Services

Should be able give immediate medical attention as per laid down SOPs.

Should be able guide the Paramedics and Support staff in Medical Emergencies.

Should be able to diagnose the medical condition and take necessary medical support.


Attributes.

  • Agile
  • Self Motivated
  • Leadership qualities
  • Critical Thinking.
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Medical Doctor

Chennai, Tamil Nadu BUILD MY BUSINESS

Posted 5 days ago

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Qualifications

  • Proficient in diagnosing and treating a wide range of medical conditions
  • Experience in managing medical records and developing treatment plans
  • Strong skills in patient communication and health education
  • Ability to perform routine medical procedures and prescribe appropriate medications
  • Excellent collaboration skills to work with other healthcare professionals
  • Medical degree from an accredited institution
  • Valid medical license to practice in Chennai
  • Proficiency in English and local languages is a plus
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Medical Doctor

Amura Health

Posted 5 days ago

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You weren't looking for this. But deep down, you've always known. there has to be more.


More truth, happiness, beauty and meaning to the way we live and care. The truth is that science has always been there. But healthcare never touched it as it is over-romanticised in the name of saving lives.


So, what would you do if someone told you that this same science that healthcare ignores ironically has the power to heal killer diseases that are considered untreatable today.


We have built a platform to identify such science, refine it and take it to humanity. Evidence-backed. Time-tested. This means you donʼt have to wait around anymore.


At Amura, Doctors start treating real patients from day one. Each doctor manages 150+ patients with full autonomy, in their own time, making their own calls.


This is your practice for the taking. Today.


Who are we?


  • Interestingly, in your own corner of the world, a hardworking team bent on hyper-excellence has quietly built a new way of medicine, a platform built on science, story, and soul.


  • Think of Amura as a "hospital on the cloud." We help people achieve the best standard of health they possibly can, taking full responsibility for their journey. We're a team of curious, ambitious individuals across all fields of work. Here, Doctors work alongside health coaches, designers, engineers, writers, and even filmmakers.


  • A cloud can reach anywhere and so can we. Your patients will be from all over the world, and you will change lives globally from your new home in Chennai. Over the last 8 years we have helped tens of thousands of people live better lives across 45 countries.


What you'll actually be doing:


  • Talking to real patients every day. Understanding their stories, their symptoms, and their goals. Soon you will be your patient's friend, with a personal connection that most Doctors are unable to have.


  • Ordering tests, interpreting blood reports, and building holistic diagnoses.


  • Creating and updating personalised care plans—nutrition, supplementation, sleep, stress, the works.


  • Handling flare-ups, doubts, frustrations, and celebrations.


  • Learning. A lot. Every week. With your peers, mentors, and specialists. And yes, you'll get to master the old-school art of taking history, and apply it in a very new-school way.


  • You'll also have regular training sessions to sharpen your clinical and communication skills.


Life at Amura.


We know the job description is supposed to sell you the role. But honestly, we cannot wait to tell you how much your life will change here.


We don't think anything like this exists anywhere in the world.


This isn't a hospital job or a clinic gig. It's a new kind of doctor's life. You will learn new concepts, new skills and new ways of thinking but more than anything you will learn to belong.


Amura Doctors are not just colleagues, they are friends, maybe even family. They are a group of young minds working together to change health care forever. You will learn from them and you will help them learn.


There is no hierarchy, no toxicity, no judgement. You are not a junior or a senior Doctor but a Doctor respected for who you are. At Amura, we have career maps instead of ladders. You get to choose how you explore and expand.


It took us 8 years to build. And now we are ready to take it to 8 billion people.


You are an Amurite if:


  • You want to treat patients from day one and be trusted to do it.
  • You're curious, open-minded, and hungry to learn fast through real practical work. You believe medicine is about people, not prescriptions.
  • You're excited by the idea of unlearning old rules and shaping something new.
  • And most importantly, you want your first job to feel like it actually means something.


Location: Perungudi, Chennai,( Soon moving to Phoenix Mall, Velachery)

Work Mode: Work from Office

Salary: 1 Lakh per month


If any of this sounds like you, write to us at or apply to job to talk to us :)

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Medical Doctor

Farakka, West Bengal Farakka Medical Diagnostic Centre Pvt. Ltd

Posted 5 days ago

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Company Description

We are situated at Farakka, Murshidabad,West Bengal.


Role Description

This is a full-time on-site role for a Medical Doctor at Farakka Medical Diagnostic Centre Pvt. Ltd. The Medical Doctor will be responsible for providing medical care, diagnosing and treating patients, conducting examinations, prescribing medications, and collaborating with other healthcare professionals.


Qualifications

  • Medical degree and valid license to practice
  • Experience in patient care and treatment
  • Strong diagnostic and decision-making skills
  • Excellent communication and interpersonal abilities
  • Ability to work well in a team
  • Knowledge of medical software and tools
  • Specialization in a specific area of medicine is a plus
  • Completion of residency program
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Medical Affairs Partner, Oncology

New Delhi, Delhi Roche

Posted 2 days ago

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At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**Position Based in Malaysia**
At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about improving the lives of patients' and are bold in both decision and action. We believe that partnering with health systems around the world can create value for patients, society and for Roche. We are uniquely positioned to realize truly integrated health solutions across pharmaceuticals, diagnostics, digital health and big data solutions; positioning us as a key partner for personalized, sustainable healthcare everywhere.
The Medical Affairs Partner (MAP) demonstrates personal purpose around improving the patient journey, as well as strong passion to create value and impact on the ecosystem. The MAP is a senior level role within the affiliate, who has decision making authority to request resources of Roche (both within the affiliate and broader network) in order to have improved impact on the patient journey.
They are a core member of the disease area pod working in close collaboration with the Patient Journey Partners (PJP). The MAP spends majority of their time in the field close to customers communicating the value of Roche's science and products to physicians, investigators and institutions. They think from an enterprise level, and will also be a member of an APAC level network working across borders, to realize and scale country outcomes by contributing to virtual, cross border, cross functional work package teams.
**The Opportunity:**
The Medical Affairs Partner has a reporting line to the Country Medical, Innovation and Regulatory Lead, serves the affiliate vision with an aligned mindset and behaviors.
+ Oversee the patient journey in its entirety, acts as a system thinker with the ability to identify shared purpose among stakeholders and cocreate with them to bring better outcomes for patients faster by translating insights into strategic and actionable recommendations.
+ Bring the inside out, to bring Roche expertise, science and knowledge to the ecosystem. Steward Roche's products through their lifecycle and supports their appropriate use, which includes sharing their merits with Healthcare Professionals (HCPs) in a truthful and balanced manner. Ensure great experiences whenever stakeholders in the ecosystem engage with Roche employees, products and services.
+ Pull in expertise and resources locally and from the network as needed, prioritize and drive solutions that deliver outcomes faster. Boldly act on key decisions and opportunities and boldly stop any activity that is not adding value.
+ Identify important data gaps and opportunities designing and supporting data generation plans to address them including phase IV studies, registries and real world evidence generation.
+ Hold an altruistic approach in supporting the global network.
+ Act as a leader, coach and mentor, who supports team working and actively contributes to the learning & development of peers across strategically aligned therapy areas, key medical affairs capabilities and engagement with healthcare professionals and patient groups.
+ Display integrity in all levels (i.e. open, honest, ethical and genuine). All Roche employees are expected to practice high standards of compliance with both external and internal policies andregulations as well as participate and be involved in SHE initiatives within the Company.
+ Supports GxP-related activities to ensure quality compliance requirements are adhered to
**Who You Are:**
+ Is self-managed and self-directed, ready to take on empowerment. Demonstrates a growth mindset, able to learn and unlearn quickly, take risks and experiment.
+ Has an enabler mindset leveraging the internal and external networks to create value, sharing back and scaling. Has outstanding partnering capabilities such as coaching, consulting, ability tolisten deeply, question and understand.
+ Willing to travel when needed.
Skills and Experience :
+ Has a deep understanding of patient journey and related treatments, medical affairs strategies & tactics including clinical research as well as broad understanding of Roche's present portfolio andfuture pipeline, such that they can work on future-based solutions. Is able to effectively sharescientific information including investigational findings through direct communications andengagement at scientific conferences with healthcare professionals and/or the scientific community.
+ Has excellent stakeholder engagement skills including partnering with Therapeutic Area Experts (TAEs) and organizations isrequired. Experience partnering with Patient Advocacy Group(PAGs) is highly desired.
+ Evidence generation skills is required. Supports relevant Product Development Medical Affairs (Global Medical Affairs) (PDMA) and Country Clinical Operationstrial, Early Access Program and Compassionate Use program activities within their diseasearea/ecosystem
+ Work efficiently and harmoniously in a cross-functional team, able to formulate cross-functionalstrategies and orchestrate cross-functional teams. Experience in agile ways of working is highlydesired.
+ Experience with medical review of promotional materials is required.
+ Ability to leverage digital means and tools is required.
+ Proficiency in English is required, fluency in the local language is desired.
+ Trained in GMP and GDP requirements for pharmaceutical
Education & Expertise:
+ Medical degree and/or PHD preferred, bachelor's degree in life sciences (eg. immunology,biomedical, biology or pharmacy) required.
+ Minimum of 3 years experience within a Medical Affairs role in Pharmaceutical, Diagnostics,Health Sciences, Biotechnology or other related fields is required.
+ Experience and expertise in **Oncology** , specifically HCC and Lung Cancer is preferred.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
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Medical Director - Clinical Oncology

Mumbai, Maharashtra Takeda Pharmaceuticals

Posted 2 days ago

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By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**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
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