592 Clinical Trial Manager jobs in India

Our client, a leading pharmaceutical company, is seeking an experienced and organized Clinical Trial Manager to oversee the execution of clinical studies in Bhubaneswar, Odisha, IN . This role requires a strategic thinker capable of managing all aspects of clinical trials, from planning and initiation to monitoring, data analysis, and close-out. You will be responsible for ensuring trials are conducted in accordance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and company protocols. Key responsibilities include developing clinical trial protocols, budgets, and timelines; selecting and managing clinical sites and investigators; overseeing the recruitment and retention of trial participants; ensuring accurate and timely data collection; and managing vendor relationships. The Clinical Trial Manager will serve as the primary liaison between the company, clinical sites, regulatory authorities, and other stakeholders. You will be instrumental in ensuring the safety of trial participants and the integrity of the trial data. This is a hybrid role, involving both office-based work for strategic planning and team collaboration, and potential travel to clinical sites for monitoring and oversight. A strong understanding of drug development processes, clinical research methodologies, and regulatory affairs is essential. Excellent leadership, communication, and project management skills are required to effectively manage complex, multi-site trials. The ideal candidate will have a proven track record of successfully managing clinical trials from start to finish.

Responsibilities:

• Develop and manage clinical trial protocols, budgets, and timelines.
• Oversee the selection, initiation, and monitoring of clinical trial sites.
• Ensure compliance with GCP, ICH guidelines, and regulatory requirements.
• Manage relationships with investigators, site staff, and vendors.
• Monitor trial progress, data quality, and participant safety.
• Facilitate the collection, review, and analysis of clinical data.
• Prepare trial-related documentation, including Investigator Brochures and Case Report Forms.
• Coordinate study close-out activities.
• Liaise with regulatory authorities as needed.
• Contribute to the development of clinical development strategies.

Qualifications:

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or a related field.
• Minimum of 5-7 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
• In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
• Proven experience in developing and executing clinical trial protocols.
• Strong project management skills with experience in budget and timeline management.
• Excellent communication, leadership, and interpersonal skills.
• Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to clinical sites as required.
• Problem-solving skills and ability to navigate complex regulatory environments.

Our client is a leading innovator in the pharmaceutical industry, and they are seeking a dedicated and experienced Clinical Trial Manager to join their fully remote team. This role is essential for the successful planning, execution, and completion of complex clinical trials, ensuring adherence to strict regulatory standards and timelines. As a remote-first Clinical Trial Manager, you will oversee all aspects of clinical trials, from protocol development through to final study report, managing budgets, timelines, and cross-functional teams. You will work closely with investigators, study coordinators, CROs, and internal stakeholders to ensure the highest quality of data and patient safety. This is a unique opportunity to contribute to life-saving therapies from the comfort of your own home.

Key Responsibilities:

• Oversee the planning, execution, and completion of assigned clinical trials in accordance with study protocols, SOPs, and regulatory requirements.
• Manage clinical trial budgets, timelines, and resource allocation effectively.
• Select, train, and manage clinical investigative sites and vendors (e.g., CROs, central labs).
• Develop and maintain strong relationships with investigators and site staff, providing oversight and support.
• Ensure the collection, review, and verification of high-quality clinical data.
• Monitor trial progress, identify potential risks, and implement mitigation strategies.
• Prepare and review essential study documents, including protocols, informed consent forms, and case report forms.
• Liaise with regulatory authorities and ensure compliance with all applicable regulations (e.g., FDA, EMA, ICH-GCP).
• Prepare clinical study reports and contribute to regulatory submissions.
• Manage study team members, fostering collaboration and ensuring efficient workflow.

Qualifications:

• Bachelor's degree in a relevant scientific discipline (e.g., Life Sciences, Nursing, Pharmacy). Advanced degree or equivalent experience strongly preferred.
• Minimum of 7 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
• Demonstrated success in managing multiple clinical trials simultaneously from initiation to closure.
• In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
• Proven experience in budget management and vendor oversight.
• Excellent project management, organizational, and leadership skills.
• Strong communication, interpersonal, and negotiation skills.
• Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and electronic trial master files (eTMF).
• Ability to work independently and proactively in a remote setting.
• Experience with a variety of therapeutic areas is advantageous.

This fully remote role offers competitive compensation and the chance to make a significant impact on medical advancements.

Our client is a leading pharmaceutical innovator dedicated to developing life-saving therapies, and they are seeking a highly experienced and results-oriented Remote Clinical Trial Manager. This pivotal role is entirely remote, allowing you to manage complex clinical trials from anywhere while contributing to cutting-edge drug development. You will be responsible for the end-to-end management of clinical trials, ensuring they are conducted in accordance with study protocols, regulatory guidelines, and company standards. Your duties will encompass study planning, site selection and initiation, budget management, data monitoring, and study close-out. You will lead and motivate cross-functional teams, including clinical research associates (CRAs), medical monitors, and data managers, fostering a collaborative and efficient research environment. A critical aspect of this role involves developing and implementing comprehensive clinical trial strategies, identifying potential risks, and devising mitigation plans to ensure timely and successful trial completion. You will also be responsible for managing relationships with clinical sites, investigators, and vendors, ensuring high-quality data collection and adherence to ethical standards. The ideal candidate will possess a deep understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial methodologies. Strong project management skills, excellent communication abilities, and a proven track record of successfully managing multiple clinical trials simultaneously are essential. We are looking for an individual with exceptional leadership qualities, strategic thinking capabilities, and the ability to drive project success in a remote, dynamic setting. This is an exceptional opportunity to play a key role in bringing novel pharmaceutical products to market and making a significant impact on global health.

Responsibilities:

• Oversee the planning, execution, and completion of clinical trials.
• Develop clinical trial protocols, study plans, and budgets.
• Select, train, and manage clinical trial sites and investigators.
• Monitor trial progress, ensuring adherence to timelines, protocols, and GCP guidelines.
• Manage relationships with external vendors and service providers.
• Ensure accurate and timely collection and review of clinical data.
• Identify and mitigate risks associated with clinical trials.
• Prepare regulatory submissions and reports.
• Lead and motivate clinical trial teams, fostering effective communication.
• Contribute to the development of new clinical research strategies and processes.

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree (Master's or Ph.D.) is a plus.
• Extensive experience in clinical trial management within the pharmaceutical industry.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in managing all phases of clinical trials.
• Strong project management, organizational, and leadership skills.
• Excellent communication, interpersonal, and negotiation abilities.
• Proficiency in clinical trial management software (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and effectively manage multiple projects in a remote setting.
• Demonstrated success in leading and motivating clinical trial teams.
• Experience in (specific therapeutic area, e.g., oncology, cardiology) is highly desirable.

Key Responsibilities

1. Data Analysis & Insights

• Gather, validate, and analyze data from clinical, operational, and administrative systems.
• Build interactive reports and dashboards using Power BI , Tableau , or similar tools to present insights to leadership and stakeholders.
• Generate both routine and ad hoc analytical outputs to support business decisions and performance reviews.

2. Performance Measurement

• Develop and monitor Key Performance Indicators (KPIs) and operational metrics across clinical and research programs.
• Identify performance trends, highlight deviations, and provide actionable insights to improve efficiency and quality.
• Present data-driven findings in a clear, visual, and strategic format for leadership teams.

3. Clinical Operations & Research Support

• Support clinical operations and clinical research teams by analyzing data related to study execution, site performance, patient enrollment, and protocol adherence.
• Provide analytical inputs for resource planning, process optimization, and cost analysis.
• Collaborate with research and operations teams to improve data governance and consistency across systems.

4. Process & Quality Improvement

• Partner with cross-functional teams to evaluate workflows, identify bottlenecks, and recommend process improvements.
• Leverage data analytics to drive initiatives that improve operational efficiency , study performance , and patient outcomes .
• Contribute to continuous improvement efforts through evidence-based analysis and metric tracking.

Qualifications & Skills

• Bachelor’s or Master’s degree in Life Sciences, Healthcare, Statistics, Data Analytics , or related discipline.
• 4–6 years of experience in data analytics within clinical operations , clinical research , or healthcare domains .
• Strong proficiency in:
• Data visualization tools: Power BI, Tableau, or Qlik
• Querying languages: SQL (Python or R a plus)
• Data handling: Advanced Excel, data cleaning, and transformation techniques
• Solid understanding of clinical operations processes , KPIs, and research data frameworks.
• Excellent analytical, problem-solving, and storytelling skills with a strong attention to detail.
• Effective communicator who can translate data insights into business actions.
• Ability to work independently with minimal supervision while collaborating across diverse teams.
• Deep functional/domain Expertise/experience with CTMS (not EDC)

About Agilisium

Agilisium is the Life Sciences industry’s premier Autonomous Agentic AI and Applied AI Services Company . We reimagine, develop, and co-develop AI-engineered business processes that are autonomous, scalable, and purpose-built for Life Sciences.

Over the past decade, we’ve established deep credibility across global pharma and biotech organizations through our specialized expertise and consistent growth:

• Everest Group – Recognized as a Leader in Life Sciences Digital Services for the Mid-Market
• Inc. 5000 – Featured among the fastest-growing companies in the U.S. for 9 consecutive years
• AWS Advanced Consulting Partner – one of the Top 13 companies globally to hold both GenAI and Life Sciences Competency Badges
• Trusted by Fortune 500 Pharma – Partnering with several Top 10 global Life Sciences companies

Agilisium continues to invest in top-tier talent to fuel innovation, scalability, and impact across the Life Sciences value chain.

Learn more:

Our client is a leading organization dedicated to community and social care, seeking a dedicated and experienced Clinical Operations Manager to oversee the smooth functioning of its services in **Visakhapatnam, Andhra Pradesh, IN**. This vital role requires a compassionate leader with a strong understanding of healthcare operations, patient care, and regulatory compliance. You will be responsible for managing the day-to-day operations of clinical services, ensuring the highest standards of patient care are maintained. This includes overseeing staff scheduling, resource allocation, quality assurance, and adherence to all relevant healthcare regulations and protocols. The ideal candidate will have a background in nursing, allied health, or healthcare administration, with demonstrable experience in managing clinical teams and facilities. You will play a key role in fostering a positive and supportive work environment for clinical staff, promoting professional development, and ensuring effective communication across all levels. Responsibilities also include managing budgets, optimizing operational efficiency, and collaborating with other departments and external stakeholders to enhance service delivery. A proactive approach to problem-solving, strong leadership qualities, and a commitment to patient well-being are essential. This is an opportunity to make a significant contribution to the health and welfare of the community.
Responsibilities:

• Manage and coordinate all daily clinical operations to ensure efficient and effective service delivery.
• Supervise, mentor, and evaluate clinical staff, fostering a culture of excellence and collaboration.
• Develop and implement operational policies and procedures to ensure compliance with healthcare regulations and standards.
• Oversee patient scheduling, resource management, and inventory control.
• Monitor quality of care, implement improvement initiatives, and ensure patient satisfaction.
• Manage departmental budgets, control costs, and optimize resource utilization.
• Liaise with medical professionals, administrative staff, and external partners to ensure seamless coordination of care.
• Ensure the maintenance of accurate and confidential patient records.
• Participate in strategic planning and contribute to the development of new services.
• Handle patient complaints and resolve operational issues promptly.

Qualifications:

• Bachelor's degree in Nursing, Allied Health Sciences, Healthcare Administration, or a related field. Master's degree preferred.
• Minimum of 5 years of experience in clinical operations management or a similar leadership role within a healthcare setting.
• Strong knowledge of healthcare regulations, patient care standards, and operational best practices.
• Proven leadership and team management skills.
• Excellent organizational, problem-solving, and decision-making abilities.
• Proficiency in healthcare management software and EMR/EHR systems.
• Strong communication and interpersonal skills.
• Ability to manage budgets and financial resources effectively.
• Commitment to providing high-quality patient care.

Our client is seeking a dedicated and compassionate Clinical Operations Specialist to join their team in Visakhapatnam. This role is integral to ensuring the seamless delivery of high-quality community and social care services. You will be responsible for coordinating patient care, managing administrative tasks, and supporting the clinical team to achieve optimal patient outcomes. The ideal candidate will possess strong organizational skills, a deep understanding of healthcare protocols, and a commitment to patient well-being.

Responsibilities:

• Coordinate and manage patient care schedules and appointments.
• Liaise between patients, families, and healthcare providers to ensure clear communication.
• Maintain accurate and confidential patient records and documentation.
• Assist in the development and implementation of care plans.
• Monitor patient progress and report any changes or concerns to the clinical team.
• Manage inventory of medical supplies and equipment.
• Ensure compliance with all regulatory requirements and ethical standards.
• Provide administrative support to the clinical staff, including preparing reports and presentations.
• Facilitate communication and collaboration among multidisciplinary care teams.
• Organize and coordinate community outreach programs and health education initiatives.
• Handle patient inquiries and provide information regarding services and appointments.
• Assist with the onboarding and training of new clinical staff.
• Implement and refine operational workflows to enhance service delivery.
• Participate in quality improvement initiatives.
• Ensure a safe and therapeutic environment for all patients.

Qualifications:

• Bachelor's degree in Nursing, Healthcare Administration, Social Work, or a related field.
• Minimum of 3 years of experience in a clinical setting or healthcare administration.
• Strong knowledge of healthcare systems, patient care protocols, and medical terminology.
• Excellent organizational, time management, and multitasking abilities.
• Proficiency in EMR/EHR systems and standard office software.
• Exceptional interpersonal and communication skills, with the ability to empathize with patients.
• Ability to work independently and as part of a team.
• Understanding of community and social care principles.
• Commitment to patient confidentiality and data privacy.
• Experience in coordinating health programs is a plus.

This is a critical role contributing to the vital services provided by our client in Visakhapatnam, Andhra Pradesh, IN . This position requires a hands-on approach and a dedication to serving the community.

Our client is seeking a dedicated and experienced Clinical Operations Manager to oversee the day-to-day operations of their healthcare facility in **Thane, Maharashtra, IN**. This critical role involves managing a team of healthcare professionals, ensuring the delivery of high-quality patient care, and optimizing operational efficiency. You will be responsible for developing and implementing clinical protocols, managing budgets, and ensuring compliance with all regulatory requirements and healthcare standards. The ideal candidate will possess strong leadership, organizational, and problem-solving skills, with a deep understanding of healthcare management principles. You will work closely with physicians, nurses, and administrative staff to foster a collaborative and patient-centered environment. Key responsibilities include staff scheduling, performance management, resource allocation, and inventory control of medical supplies. Experience in quality improvement initiatives and patient safety programs is highly valued. You will also play a key role in strategic planning and operational development to enhance service delivery and patient outcomes. This position requires excellent communication and interpersonal skills to effectively liaise with patients, families, and external stakeholders. A thorough understanding of healthcare regulations, such as HIPAA and local health guidelines, is essential. The Clinical Operations Manager will lead efforts to improve patient satisfaction scores and streamline clinical workflows. You will be responsible for identifying areas for process improvement and implementing effective solutions. This role involves overseeing departmental budgets, ensuring financial targets are met while maintaining optimal service levels. The successful candidate will have a passion for healthcare excellence and a proven ability to lead and inspire teams in a demanding clinical setting. You will also be involved in the recruitment and onboarding of new clinical staff. Ensuring a safe and efficient working environment for all staff and patients is a top priority. This is an excellent opportunity for a seasoned healthcare professional to take on a leadership role within a reputable organization.

Responsibilities:

• Manage and supervise all clinical and administrative staff within the facility.
• Ensure the delivery of high-quality, patient-centered care.
• Develop, implement, and enforce clinical policies and procedures.
• Oversee departmental budgets and manage financial resources effectively.
• Ensure compliance with all healthcare regulations, licensing, and accreditation standards.
• Manage staff scheduling, performance, and professional development.
• Monitor patient satisfaction and implement strategies for improvement.
• Optimize clinical workflows and operational efficiency.
• Maintain adequate inventory of medical supplies and equipment.
• Collaborate with physicians and other healthcare providers to ensure coordinated patient care.

Qualifications:

• Bachelor's degree in Nursing, Healthcare Administration, Business Administration, or a related field. A Master's degree is preferred.
• Minimum of 5 years of experience in healthcare management or a related leadership role.
• Proven experience in clinical operations, patient care delivery, and staff management.
• Strong knowledge of healthcare regulations, accreditation standards, and best practices.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in healthcare management software and EMR/EHR systems.
• Demonstrated ability in budget management and financial planning.
• Strong problem-solving and decision-making abilities.

This role offers a competitive salary, comprehensive benefits, and the chance to make a meaningful impact on patient lives within the **Thane, Maharashtra, IN** community.

Our client is seeking an experienced and dedicated Clinical Operations Manager to oversee the smooth and efficient running of their community health and social care services. This crucial role involves managing day-to-day operations, ensuring high standards of care, and leading a team of dedicated professionals. You will be responsible for resource allocation, staff supervision, and the implementation of operational policies and procedures designed to optimize patient and client outcomes.

Key Responsibilities:

• Supervising and mentoring a team of healthcare professionals, including nurses, social workers, and support staff.
• Managing daily operational schedules, ensuring adequate staffing levels and efficient service delivery.
• Developing, implementing, and monitoring adherence to clinical protocols and quality standards.
• Overseeing patient and client care pathways, ensuring a compassionate and effective approach.
• Managing budgets, including resource allocation, expense tracking, and financial reporting.
• Ensuring compliance with all relevant healthcare regulations and standards.
• Collaborating with external healthcare providers and community organizations to enhance service integration.
• Handling patient/client grievances and feedback to ensure continuous improvement.
• Implementing training programs and professional development opportunities for staff.
• Maintaining accurate and up-to-date records and documentation.

The ideal candidate will hold a relevant degree in Healthcare Management, Nursing, Social Work, or a related field, coupled with a minimum of 5 years of experience in a supervisory or management role within the healthcare or social care sector. Demonstrated leadership abilities, strong organizational skills, and a deep understanding of clinical operations are essential. Excellent communication, problem-solving, and interpersonal skills are required to manage a diverse team and interact effectively with clients and stakeholders. Familiarity with healthcare information systems and a commitment to continuous quality improvement are crucial. This is an on-site position based in Thane, Maharashtra, IN .

Company 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
To enable AbbVie's emergence as a world class R&D organization, the Site Management and
Monitoring (SMM) Country/District COM plays a leadership role accountable for driving the business
of SMM within a Country/District(s) by providing oversight and direction to SMM staff; accountable
for the on time, within budget and quality delivery of the clinical studies. Promotes best practice;
identifies infrastructural improvements and implements action plan to ensure Clinical Field
Operations (CFO) and business objectives are successfully met; ensures alignment of local activities
with regional/global initiatives. The role reports into the Site M&M Leadership and serves as a single
point of accountability for the SMM deliverables within a Country/Disitrct(s) and influences and
aligns within Development Operations, and with Global Medical Affairs (GMA), and other key
stakeholders across the organization.
Responsibilities :
List up to 10 main responsibilities for the job. Include information about the accountability and
scope.
Manages/oversees site/country or district related activities as they relate to AbbVie clinical studies
(e.g. country feasibility, site evaluation/selection and activation, contracts/budget negotiation,
regulatory/EC submissions startup, issue management, relationship management, monitoring, site
closure). Accountable for the on-time and within budget execution of all clinical trials within a
Country/District(s). Provide local regulatory and legal requirement expertise.
Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices
(GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to
quality standards in conducting clinical research. Monitor regulatory reforms and industry trends
within country / region. Conduct and/or implement impact analysis of all significant changes to
conform with updated regulatory / industry regulations affecting conduct of clinical studies.
Ensures audit and inspection-readiness at all times. Country contact for regulatory agency
questions related to monitoring processes and procedures. Drive CAPA preparation and
implementation.
Accountable for managing country/district resources including need identification, timely hiring and
allocation, and managing changes to hiring plan. Responsible for staff recruitment and retention
plans.
Accountable for functional budget planning and administration.
Provide leadership to the Country/District and be accountable for growth and development of a
world class workforce that role models AbbVie behaviors.
Drives a learning environment and ensures continuous improvement in Country/District(s)
performance by using innovative approaches, active analysis of Key Performance Indicators,
metrics and milestones. Driving simplicity in process and approach, and enhancing agility.
Accountable for ensuring SITE M&M leadership, collaboration and teamwork across all key
stakeholders within the Country(s).
May lead global Task Forces and Initiatives. Interacts with peers within the industry to stay
abreast of regulatory landscape, raise AbbVie' s profile in the R&D community. Accountable for
driving affiliate R&D Community goals in partnership with GMA.
Qualifications
Qualifications :
List required and preferred qualifications up to 10). Include education, skills and experience.Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing,
Pharmacy) preferred.
Site Monitoring Experience: Minimum 3 years. Preferably having monitored and/or managed a
study within a Country from start to close.
Experience in functional budget planning, resource planning & assignment, quality management in
a Country lead capacity preferred.
At least 2 years of experience in line management of staff including acquisition of talent,
performance management, growth and development, managing employee relations, coaching and
mentoring of staff and teams preferred.
Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives
and drive smart decision making.
Excellent interpersonal skills with the ability to communicate persuasively and with clarity,
flexibility and adaptability to changing requirements, resourcefulness and creativity. Demonstrated
proactive and positive team player.
Exhibits strong planning and organizational skills and high level of flexibility in a dynamic
environment with experience leading (within country or region) projects with competing deadlines;
Experience across multiple Therapeutic Areas and Study Phases.
Demonstrating business ethics and integrity.
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.
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