9 Nursing Administration jobs in India

Director, Clinical Data Management

Hyderabad, Andhra Pradesh Amgen

Posted 2 days ago

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Job Description

**Director Clinical Data Management**
**Live**
**What You Will Do**
Let's do this. Let's change the world. The Amgen Global Clinical Data Management team is looking for an experienced Director to lead our data management team on the aspiration of optimizing and delivering an industry admired clinical evidence platform to deliver innovative medicines to patients with unmet medical needs.
The Director is accountable for leadership and oversight of the data management organization; ensuring operational excellence and consistency in clinical trial execution. They are accountable for building and developing a high performing internal data management team, as well as ensuring engagement and alignment of Amgen's strategy and priorities with the Functional Service Provider (FSP).
The Director is also part of the Global Study Operations (GSO) leadership team, accountable for the delivery of quality clinical trials through industry-leading execution of innovative processes, strong cross-functional partnerships, and best-use of clinical systems and analytics to guide site and study operations. The role will support acceleration of clinical programs and other continuous improvement efforts, applying innovative thinking in shaping future strategy.
Our Global Clinical Data Management Team:
The Global Clinical Data Management Team comprises approximately 50 people. The three Directors, as part of the wider GSO organization and reporting into the Executive Director, Global Study Operations, work together to meet the demands of an industry leading, fast paced, high throughput organization with a commitment to compliance, quality and standards.
Director Clinical Data Management role overview:
You will lead and manage Data Management (DM) teams within a specific DM operational business unit. The Director will set and drive forward the vision and strategy for DM as a member of the DM and GSO Leadership Team.
Responsibilities:
+ Oversight of a distinct DM operational unit (e.g. therapy area, cross-product area)
+ Recruiting, managing and developing staff
+ Global resource planning and assignments
+ Setting of functional goals and objectives
+ Creating and implementing GSO & DM strategies developing, reviewing, implementing and enforcing data standards
+ Ensuring DM processes/systems meet regulatory and business requirements
+ Be an active member of the Leadership Team to provide a foundation for GSO success
Key activities will include:
+ Team management including performance, coaching and development
+ Develop, review and implement policies, SOPs and associated documents affecting DM globally
+ Set vision, strategy and direction for DM group; develop annual goals and objectives
+ Accountable for and oversee DM FSP relationships; ensuring goals of product areas and systems groups can be met via the FSP
+ Define and maintain Service Level Agreements and Key Performance Indicators; including oversight of quality and CAPA management
+ Governance oversight -ensure visibility into performance of FSPs to the department
+ Sponsor, Lead and participate in cross functional working groups
+ Resource and budget management for global function Ensure adequate training and capability within area and be accountable for staff compliance with all DM processes
+ Vendor management (development of strategies, contract management, relationship management, etc)
+ Respond to audit/inspection findings
+ Be accountable for and oversee all study deliverables and submission activities for products within group
+ Ensure that status information on DM activities is available and is acted on as needed
**Win**
**What We Expect Of You**
We are all different, yet we all use our unique contributions to serve patients. The data management professional we seek is a collaborator with these qualifications.
Basic requirements:
+ **18 to 23** years of data management experience
Preferred Experience:
+ Master's degree or equivalent in life science, computer science, business administration or related discipline
+ 10+ years of extensive experience in data management in the Pharmaceutical or Biotech arena
+ 8+ years of experience in rare disease therapeutic area, in a leadership role
+ Broad experience of working in a global organization
+ Experience at or oversight of outside vendors (CRO's, central labs, imaging vendors, etc)
+ 8+ years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
+ Strategic and innovative thinker with experience of driving operational excellence
+ Excellent relationship building skills with the ability to influence and make business impact
+ Ability to work collaboratively cross functionally with ability to influence and drive decisions
+ Proven experience within oversight of clinical research suppliers
+ Project management
+ Previous experience in a global, matrix organization
+ Excellent organizational and interpersonal skills
+ Ability to anticipate and problem solve challenging issues
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AVP, Clinical Data Management

Hyderabad, Andhra Pradesh Amgen

Posted 2 days ago

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Job Description

**JOIN AMGEN'S MISSION OF SERVING PATIENTS**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Associate Vice President, Clinical Data Management**
**Live**
**What you will do**
Let's do this. Let's change the world. The Associate Vice President, Clinical Data Management is a member of the Global Development Operations (GDO) leadership team and is a strategic partner to the R&D organization.
**The AVP will lead Amgen's Clinical Data Management function within GDO, ensuring the highest quality of clinical data collection, processing, and analysis to support regulatory submissions and clinical development programs. This role is responsible for the strategic direction, leadership, and operational oversight of data management processes supporting clinical trials across all therapeutic areas and phases.**
This AVP will collaborate closely with cross-functional teams including clinical operations, biostatistics, regulatory affairs, and quality to drive data integrity and compliance with global regulatory standards.
The role requires a visionary leader with deep expertise in CDM and a proven ability to scale and lead global teams in a complex matrix environment.
**Responsibilities:**
+ **Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals.**
+ **Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases.**
+ **Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows.**
+ Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums.
+ Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance.
+ **Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization.**
+ Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues.
+ Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions.
+ Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics.
+ Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data.
+ Build and maintain strategic relationships with CROs, vendors, regulatory authorities, and industry organizations to advance CDM excellence.
+ Influence internal leadership and functional partners to promote data-driven decision-making across clinical programs.
+ Lead audit readiness efforts and promote a culture of continuous improvement and compliance within the CDM function.
+ Implement protocols and tools to ensure data security, integrity, and risk management across all platforms and studies.
+ Optimize staffing, outsourcing strategies, and technology investments to improve cost-efficiency, scalability, and delivery timelines.
**Win**
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an experienced leader with the following qualifications.
**Basic Qualifications:**
+ **Bachelor's or master's degree with 25+ years of data management experience AND**
+ **10 to 15 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources**
**Preferred Qualifications:**
+ Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment.
+ **Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM).**
+ Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen's global clinical development efforts.
+ Expertise in AI/ML-driven data management solutions, automation, and advanced analytics.
+ **Understanding of clinical data standards (CDISC, SDTM, ADaM).**
+ **Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions**
+ Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management.
+ Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams.
+ **Experience managing FSP relationships and technology implementations (EDC, CTMS, RWD/RWE).**
+ **Knowledge of emerging trends in digital health, data governance, and data privacy regulations (GDPR, HIPAA).**
+ Familiarity with decentralized trial models and digital health technologies.
They will also embody the Amgen leadership attributes which are:
+ **Inspire:** Create a connected, inclusive, and inspiring work environment that empowers talent to thrive
+ **Accelerate:** Enable speed that matches the urgency of patient needs by encouraging progress over perfection
+ **Integrate:** Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders
+ **Adapt:** Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
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Associate Director, Clinical Program Management

Bengaluru, Karnataka Takeda Pharmaceuticals

Posted 2 days ago

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Job Description

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**
**_OBJECTIVES/PURPOSE_**
+ Lead study operational strategy and planning and oversee execution of clinical studies for the assigned clinical program(s), supporting clinical strategy defined in Clinical Development Plan (CDP).
+ In close collaboration with Clinical Operations Program Lead (COPL) and Clinical Study Manager (CSM):
+ Responsible for oversight of the execution of studies in the assigned clinical program(s) in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs), on schedule and on budget.
+ Oversight of strategic CRO partners and/or other vendors to meet Takeda's obligations described in ICH-GCP and Takeda's business objectives.
+ Represent Clinical Operations to contribute to CDP by providing regional operational expertise and strategic, inputs including study feasibility, budget, and timeline for assigned clinical programs
**_ACCOUNTABILITIES_**
+ Accountable for developing regional operational strategy for assigned clinical studies.
+ Contribute to the translation of CDP into an optimal operational strategy and plan. Lead assessment of various scenarios operational for optimal execution of CDP.
+ Collaborate with key investigators to reflect feasible and realistic operational inputs to CDP and ensure timeline and quality of studies meet the needs of CDP.
+ Provide subject matter expertise and operational input into protocol synopsis and protocol, obtaining opinions in terms of study execution from key investigators, as appropriate.
+ Challenge study team to ensure that operational feasibility, inclusive of patient and site burden and that timelines meet the needs of CDP.
+ Validate budget and ensure impacts are adequately addressed.
+ Participate in site selection process, with a focus on providing country insights, and therapeutic expertise to ensure alignment between study execution plan and program strategy.
+ Responsible for clinical study budget planning and management, and accountable for external spending related to clinical study execution. Works closely with relevant stakeholders (strategic CRO partners, other vendors, CSM, COPL, and Program Management, Outsourcing, and Finance) to ensure the accuracy of budget spending on a regular basis.
+ Oversee strategic CRO partners and other vendors to ensure the overall operational execution and delivery of the assigned clinical studies in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs), on schedule and on budget. Oversight includes but is not limited to:
+ Review and approval of key risk-based monitoring documents/plans, periodic review of outputs, decisions, and actions related to risk-based monitoring.
+ Documented review and monitoring of issues, risks and, decisions at the study level.
+ Support the identification of trends across sites and/or the study.
+ Review and provide clinical operations expertise into clinical documents related to the drug development process:
+ Creation and maintenance of clinical trial materials, such as Investigator Brochures, study synopsis & protocols, clinical study reports, etc.
+ Preparation of key regulatory meetings, as appropriate.
+ Collaborate with cross-functional counterparts and strategic CRO partners/other vendors to ensure inspection readiness and lead Clinical Operations aspects of inspection readiness activities and act as subject matter expert during regulatory inspections.
+ Actively seek new ways of working more efficiently to meet the needs of clinical development, such as cost-reduction, time-savings, efficiency, and quality.
+ Participate in Business Development/in-licensing/alliances evaluations by providing operational due diligence.
+ Responsible for talent development, including training and mentoring less experienced staff.
+ Seek an efficient way to maximize operational excellence in the cross-regional collaboration (e.g. Japan & Asia) with innovative ideas.
**_CORE ELEMENTS RELATED TO THIS ROLE_**
**Program**
+ Provide operational expertise and strategic inputs to the development of CDP and lead assessment of various operational scenarios for optimal execution of CDP.
+ Recognized as a clinical operations expert by other functions and stakeholders across R&D.
**Organization**
+ Actively seek new ways of executing studies more efficiently to meet the needs of clinical development and encourage the function.
**Capability development**
+ In addition to the self-development, think about supporting the development of Clinical Operations staff by sharing knowledge and experience with them.
**_DIMENSIONS AND ASPECTS_**
**Technical/Functional (Line) Expertise**
+ Have sufficient knowledge of regulatory and compliance requirements and guidance for clinical development, assigned Therapeutic Areas (TAs), project governances, and working models and accurately assess the impact of these on the assigned TA and programs.
**Leadership**
+ Demonstrate ability to work across functions, regions, and cultures.
+ Embraces and demonstrates a diversity and inclusion mindset and role models these behaviors for the organization.
+ Train and develop less experienced staff with an awareness of mid- to long-term function goals and clinical development.
**Interaction**
+ Cultivates a broad network of relationships throughout Takeda, with affiliates and external partners, in the industry and area of expertise.
+ Effectively represents function in negotiations with the ability to resolve conflict in a constructive manner.
**Innovation**
+ Recommend and influence the ideal model and approach for meeting the program goals and TA operational strategies.
+ Challenge status quo and bring forward innovative solutions.
**Complexity**
+ Work in global ecosystem (internal and external) with a high degree of complexity.
**Decision-making and Autonomy**
+ Provide input and implement appropriate strategies with understanding the goals of the function and assigned TA.
**_EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:_**
+ Bachelor's Degree or international equivalent required, Life Sciences preferred.
+ Innovate and challenge peers and teams to think and work differently; Work independently, excel at solving issues without the need for support, but is effective at enlisting support for specific asks when necessary.
+ Participate and lead clinical operations in cross-functional initiatives and workstreams that affect clinical operations; Adapt ways of working to the function's current state and formulate strategic plans to work within the existing framework.
+ Capable of assessing gaps cross-functionally and can take a supportive role in leading changes that benefits the function as it related to clinical trial execution and study management.
+ Encourage and provide input, suggestions, and support for competency building within the organization.
+ Demonstrated excellence in study management, including scenario assessment, risk assessment and contingency planning.
+ Excellent teamwork, communication, organizational, interpersonal, conflict resolution and problem-solving skills.
+ Talent development skills to enhance capabilities.
+ Experience of 10+ years in pharmaceutical industry and/or clinical research organization, including 7+ years of clinical study management/oversight.
+ Experience must include Phase 1, 2, 3 studies and global/international studies or programs.
+ Experience in more than one therapeutic area.
+ English (fluently in oral and written communication)
+ Local language (fluently, a native level)
**TRAVEL REQUIREMENTS:**
+ Requires approximately 5-20 % travel, including overnight and local/international travel to other Takeda sites, strategic partners, and therapeutic area required travel.
**Locations**
IND - Bengaluru
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
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Clinical Data Management - DA/SME

400008 Mumbai, Maharashtra ₹300000 - ₹500000 month 2coms

Posted 528 days ago

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Permanent

·    Perform Migrations / Set up / Close out activities apart from Study Conduct activities under supervision and quality checks

·    Triage of Safety cases

·    Oversight of data discrepancy management

·    Owner of study documentation, including completeness, accuracy, and performing periodic review of eTMF/TMF

·    Responsible for compiling HoS content

·    Conduct the protocol amendment impact assessment and complete appropriate documentation

·    Manage migration and audit trail reports

·    Create slides for study-specific EDC investigator training

·    Generate all study related reports, status updates, and carries out all study related email conversation and communication with internal stakeholders and Client.

·    Provide study specific training to data manager (DM)

·    Contribute to the Data Management Plan (DMP)

·    Request DTS creation and ensure DTS finalized and complete for any LSH loads

·    Execute data review per IDRP (e.g. SAE reconciliation, PK reconciliation, short term-long term reconciliation)

·    Manage table in EDC for study specific inclusion/exclusion data (SDTM related to protocol)

·    Manage global and study-specific data entry conventions

·    Facilitate versioning, including Unlock/audit trail review & Archival process

·    Knowledgeable of study protocol to provide secondary feedback to SD/DWA for consistency and completeness of clinical database/study design

·    Timely communication with key stakeholders on issues and risks, including

o   Brings CDR, DWA, and SD together to discuss post-production changes when identified

·    Provide critical information to PL who will communicate with study team

·    Log any action issues into DS Hub and resolve outstanding issues assigned to DA

·    Mange assigned activities to meet milestone dates

·    Ask questions to get information needed to meet end goals

·    Manage programming only changes (Move to DWA for LSH and SD for EDC when SOP and T11/12 updated)

What you need

·    A Graduate/Post Graduate/Doctorate degree in Life sciences/ Pharmacy/Medical sciences or equivalent degree

·    Minimum 2 years to 6 years of experience in clinical data management

·    Proactively communicate ownership of studies

·    Critical thinking to identify root causes and best solutions for data discrepancy management

·    Confidence to have tough conversations and make challenging decisions

·    Enables an environment of open and honest communication and critical thinking within DSS study team

·    Influence internal team to meet timelines by holding stakeholders accountable

·    Ability to work with different personalities to get the work done

·    Willingness to seek out information to accomplish goal

·    Proactive communication

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Director of Operations (Healthcare Management)

560001 Bangalore, Karnataka ₹150000 Annually WhatJobs

Posted today

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full-time
Our client, a leading healthcare services provider, is seeking a highly experienced and strategic Director of Operations to oversee their expanding network of facilities. This is a critical remote leadership role responsible for ensuring the efficient and effective delivery of healthcare services across multiple locations. You will be instrumental in developing and implementing operational strategies, optimizing resource allocation, and maintaining the highest standards of patient care, safety, and regulatory compliance. Key responsibilities include managing budgets, overseeing financial performance, driving operational efficiency, and leading teams of healthcare professionals. The ideal candidate will possess a deep understanding of healthcare operations, patient flow, clinical workflows, and healthcare information systems. Strong analytical skills are required to monitor key performance indicators (KPIs), identify areas for improvement, and implement data-driven solutions. You will work closely with medical staff, administrators, and external stakeholders to foster a collaborative environment and achieve organizational goals. Experience in quality improvement initiatives, risk management, and change management within a healthcare setting is essential. This role demands exceptional leadership qualities, including the ability to motivate and inspire teams, communicate effectively across all levels of the organization, and navigate complex regulatory landscapes. If you are a visionary leader with a passion for healthcare excellence and a proven ability to manage complex healthcare operations remotely, this is an outstanding career opportunity.

Key Responsibilities:
  • Develop and execute strategic operational plans for healthcare facilities.
  • Oversee daily operations, ensuring optimal patient care and service delivery.
  • Manage budgets, financial performance, and resource allocation effectively.
  • Ensure compliance with all healthcare regulations and accreditation standards.
  • Lead and mentor clinical and administrative teams to foster a culture of excellence.
  • Drive operational efficiency and implement process improvements.
  • Monitor key performance indicators and implement data-driven strategies.
  • Manage risk, safety, and quality improvement initiatives.
  • Collaborate with medical leadership and stakeholders to achieve organizational objectives.
  • Oversee facility management and maintenance operations.
Qualifications:
  • Master's degree in Healthcare Administration, Business Administration, Public Health, or a related field.
  • 7-10 years of progressive experience in healthcare operations management.
  • Proven ability to lead and manage complex healthcare organizations remotely.
  • In-depth knowledge of healthcare operations, regulations, and best practices.
  • Strong financial acumen and experience in budget management.
  • Excellent leadership, communication, and interpersonal skills.
  • Experience with healthcare information systems (HIS) and electronic health records (EHR).
  • Demonstrated success in quality improvement and patient safety initiatives.
  • Strategic thinking and problem-solving abilities.
  • Familiarity with healthcare accreditation processes (e.g., NABH, JCI).
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Discharge Nurse Manager

Mumbai, Maharashtra Sir H.N. Reliance Foundation Hospital & Research Centre

Posted 25 days ago

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full-time

Job Title: Discharge Nurse Manager


Department: Nursing / Patient Services

Location: Sir H. N. Reliance Foundation Hospital, Girgaon, Mumbai

Qualification: B.Sc. Nursing (Mandatory)

Experience: Minimum 4 years in clinical nursing or hospital operations (preferably in discharge coordination or patient services)

Shift Timing: Rotational shifts between 7:00 AM 10:00 PM (including weekends on a roster basis)


About Sir H. N. Reliance Foundation Hospital:

Sir H. N. Reliance Foundation Hospital is a 345+ bedded hospital, one of Mumbais leading multi-specialty quaternary care hospitals located in Charni Road, South Mumbai.

  • Renowned for patient-centric care , advanced infrastructure, and compassionate service
  • NABH-accredited with globally benchmarked clinical protocols and technology
  • Committed to clinical excellence, seamless care delivery , and dignified patient experiences


Role Overview:

The Discharge Nurse Manager plays a vital role in coordinating and managing the complete discharge process from the point of provisional discharge until the patient physically exits the hospital. This role requires a smart, proactive professional with strong communication skills, clinical awareness, and the ability to manage multiple stakeholders efficiently to ensure a smooth and timely discharge experience for every patient.


Key Responsibilities:

1. Discharge Process Coordination:

  • Take ownership once the discharge is marked as provisional
  • Liaise with treating consultants and residents for timely preparation of discharge summaries
  • Review and validate all discharge documentation for accuracy and completeness

2. Patient & Family Education:

  • Clearly explain all post-discharge instructions including:
  • Medications
  • Dietary guidance
  • Activity restrictions and wound care
  • Follow-up appointments and red flags
  • Use clinical awareness to answer patient/family queries and escalate where deeper medical input is required

3. Interdepartmental & Stakeholder Communication:

  • Collaborate with:
  • Billing & Finance for final bill settlement
  • TPA/Insurance Desk for documentation, approvals, or delays
  • Pharmacy, Dietary, Transport, Housekeeping , etc. to ensure discharge readiness
  • Ensure all non-clinical patient concerns (laundry, food, personal items, room queries) are resolved before exit

4. Discharge Experience Oversight:

  • Be the single point of contact for patients and families during discharge
  • Identify and address bottlenecks to ensure smooth discharge experience
  • Maintain real-time escalation logs and process feedback


Candidate Requirements:

  • B.Sc. Nursing with valid nursing council registration
  • Minimum 4 years of clinical or hospital operations experience
  • Strong verbal and written communication skills in English, Hindi, and preferably Gujarati and Marathi
  • Confident, smart, and proactive in stakeholder management (Doctors, Billing, TPA, Admin, etc.)
  • Good understanding of basic clinical practices to assist with patient education and discharge clarity
  • Compassionate and professional attitude in patient-facing situations


Language Requirement:

  • We are looking to hire a minimum of 6 nurses who are fluent in Gujarati , in order to support and communicate effectively with our large Gujarati-speaking patient population.


What We Offer:

  • The opportunity to be part of one of Indias most respected and modern healthcare institutions
  • A supportive, learning-focused, and high-performance work culture
  • Exposure to complex hospital operations and end-to-end patient experience management


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Nurse Manager – Oncology Daycare

Mumbai, Maharashtra Sir H.N. Reliance Foundation Hospital & Research Centre

Posted 4 days ago

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Job Description

full-time

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

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Clinical Nurse Manager - Community Care

560001 Bangalore, Karnataka ₹1200000 Annually WhatJobs

Posted 13 days ago

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Job Description

full-time
Our client, a leading provider of community-based healthcare services, is seeking an experienced and compassionate Clinical Nurse Manager to oversee their operations. This vital role involves leading a team of dedicated healthcare professionals, ensuring the highest standards of patient care, and managing the day-to-day operations of our community care services. You will be responsible for staff supervision, patient assessment, care planning, and ensuring compliance with all regulatory and clinical guidelines. The ideal candidate will possess strong clinical skills, exceptional leadership abilities, and a deep commitment to serving the community.

Responsibilities:
  • Lead, mentor, and manage a team of nurses, healthcare assistants, and support staff.
  • Oversee the provision of high-quality patient care in community settings, including home visits and clinic-based services.
  • Conduct comprehensive patient assessments, develop individualized care plans, and ensure their effective implementation.
  • Monitor patient progress and outcomes, making adjustments to care plans as necessary.
  • Ensure adherence to all clinical protocols, safety procedures, and regulatory requirements.
  • Manage staff scheduling, performance evaluations, and professional development.
  • Collaborate with physicians, therapists, and other healthcare professionals to coordinate patient care.
  • Maintain accurate and timely patient records and documentation.
  • Manage resources efficiently, including supplies and equipment.
  • Act as a primary point of contact for patients, families, and external healthcare providers.
Qualifications:
  • Registered Nurse (RN) with a Bachelor of Science in Nursing (BSN) or equivalent qualification.
  • Master's degree in Nursing, Healthcare Administration, or a related field is preferred.
  • 5+ years of clinical nursing experience, with at least 2 years in a supervisory or management role.
  • Experience in community health, home healthcare, or public health nursing is highly desirable.
  • Strong leadership, decision-making, and problem-solving skills.
  • Excellent communication, interpersonal, and patient advocacy skills.
  • Proficiency in electronic health record (EHR) systems.
  • Knowledge of relevant healthcare regulations and standards.
  • Current nursing license and any required certifications.
  • Ability to work effectively in a dynamic and challenging environment.
This is an excellent opportunity for a dedicated nursing leader to make a significant impact on the health and well-being of individuals within the community. Join our compassionate team and contribute to providing exceptional care. Location: Bengaluru, Karnataka, IN .
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Senior Management Consultant - Healthcare Strategy

400601 Thane, Maharashtra ₹2200000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a prestigious management consulting firm with a strong focus on the healthcare sector, is seeking a highly experienced Senior Management Consultant specializing in healthcare strategy. This role is fully remote, allowing you to leverage your expertise to advise leading healthcare organizations on critical strategic challenges. You will be instrumental in helping clients navigate complex market dynamics, optimize operational performance, and drive sustainable growth. Responsibilities include conducting in-depth market analysis, developing strategic plans, facilitating change management initiatives, and building strong client relationships. The ideal candidate possesses deep industry knowledge, exceptional analytical skills, and a proven ability to deliver impactful solutions.

Key responsibilities:
  • Lead client engagements focused on healthcare strategy, including market entry, service line expansion, mergers & acquisitions, and organizational transformation.
  • Conduct comprehensive market research, competitive analysis, and financial modeling to support strategic recommendations.
  • Develop and present strategic roadmaps, business cases, and implementation plans to senior client executives.
  • Advise clients on operational improvements, cost optimization, and performance enhancement initiatives within the healthcare ecosystem.
  • Facilitate workshops and stakeholder meetings to drive consensus and alignment on strategic objectives.
  • Manage project teams, ensuring timely and high-quality delivery of project milestones.
  • Build and maintain strong, trusted advisor relationships with key client stakeholders across hospitals, health systems, and payers.
  • Contribute to business development efforts, including proposal development and thought leadership.
  • Stay current with industry trends, regulatory changes, and innovative healthcare models.
  • Mentor and develop junior consultants, fostering their growth within the firm.

The ideal candidate will hold an MBA or a Master's degree in a related field (e.g., Health Administration, Public Health, Finance), along with a Bachelor's degree. A minimum of 6-8 years of experience in management consulting, with a dedicated focus on the healthcare industry, is required. Demonstrated experience in healthcare strategy development, market analysis, and operational consulting is essential. Excellent analytical, problem-solving, communication, and presentation skills are paramount. Candidates must be comfortable working independently and collaboratively in a remote environment. The ability to travel occasionally for client meetings may be required, but the role is primarily remote, serving clients across the region, including those in the vicinity of Thane, Maharashtra, IN .
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