1,370 Clinical Trial Manager jobs in India

Company Description

QREC Clinical Research LLP is a Contract Research Organisation with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE). We provide comprehensive services to the healthcare industry, doctors, and researchers in clinical trials (Phase 3 & 4), real-world studies, observational studies, PMS, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico marketing globally. Our achievements include contributions to 450+ brand plans, 162+ real-world studies, 153+ investigator-initiated studies, and more. With a skilled team and extensive doctor and patient databases, QREC is committed to excellence in clinical research.

Role Description

This is a full-time on-site role for a Clinical Trial Assistant located in Jaipur. The Clinical Trial Assistant will support the management and oversight of clinical trials, maintaining the Trial Master File (TMF), assisting in clinical operations, coordinating research activities, and ensuring compliance with regulatory requirements. Daily tasks include coordinating with research teams, managing documentation, and assisting with data collection and analysis.

Qualifications

• Communication skills
• Experience with Trial Master File (TMF)
• Research and Clinical Trials experience
• Clinical Operations experience
• Attention to detail and excellent organizational skills
• Ability to work independently and as part of a team
• Bachelor's degree in Life Sciences, Medicine, or related field
• Previous experience in a similar role in the healthcare industry is a plus

Job Summary:

We are seeking The Clinical Trial Team Leader oversees and manages the execution of clinical trials, ensuring compliance with regulatory standards, timelines, and quality metrics. This role involves cross-functional leadership, strategic planning, and direct supervision of study teams to deliver successful trial outcomes. Key Responsibilities:

•Lead cross-functional teams, including operations managers, team leads, quality analysts, and support staff, to ensure seamless service delivery and collaboration.

•Providementorshipandguidancetoteammembers,fosteringacultureofaccountability, innovation, and continuous improvement.

• Monitorprocessperformance, identifying and addressing risks, issues, and deviations to maintain service excellence.

• Over see client onboarding, workflow management, quality assurance, and process optimization to ensure compliance with industry standards and client expectations.

• Prepare and present operational reports, performance updates,andinsights to senior management and stakeholders.

• Serve as the primary point of contact for clients, ensuring professional and courteous communication.

• Maintain strong client relationships by providing clear, accurate, and proactive support to meet business objectives. Areas of Expertise

• Medical Record Interpretation: Proficient in analyzing various components of medical records, with strong understanding of confidentiality standards and data security protocols for research subjects.

• Medical Terminology & Clinical Knowledge: Solid foundation in medical terminology, anatomy, and physiology through formal coursework and hands-on experience in clinical and research environments.

• Oncology Research Experience: Prior experience working in oncology-focused research settings, contributing to clinical trials and patient data management.

• Electronic Medical Records (EMR) & Clinical Systems: Extensive knowledge of EMR platforms such as Power Chart, and expertise in using clinical trial management systems like OnCore, along with other specialized data entry tools. SSPL - Unauthorized access, reproduction, or distribution of this document is prohibited. Required Skills and Qualifications:

• Education: o Bachelors degree in pharmacy or Life Sciences.

• Experience: o Minimum (5-8+) years of experience in clinical research in BPO / KPO with at least (2-4+) years in a leadership or management role.

• Communication Skills: Excellent written and verbal communication.

• Other Skills: o Strong organizational and multitasking abilities. Work Environment:

• Work from office. Compensation and Benefits:

• Competitive salary and benefits, including health insurance and paid time off. This position is an excellent opportunity for individuals looking to advance their careers in Clinical Trial

Candidates Please call on the below Number :

HR lead (Vijay Jadhav ) Mob :

Email :-

Medpace is currently looking for
Clinical Trial Manager (CTM)
to lead global clinical research studies. This position is fully office-based in our Mumbai, India office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

Responsibilities
The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.

Qualifications

• Bachelor's degree in a health related field (Master's degree or PhD is preferred);
• At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable and comfortable in working in a global environment.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

• 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.

• 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.

Job Title: Clinical Trial Manager

Onsite - Hyderabad

Company Overview: We eteraflex connects a fast-growing global CRO specializing in oncology, rare diseases, and immunotherapies. Our mission is to accelerate access to innovative treatments by combining regulatory precision with deep site engagement, particularly in complex government-led research environments across India.

Position Summary: We are seeking an experienced Clinical Trial Manager (CTM) to lead the execution of Phase I, II and III oncology studies at key national institutions in India. This role is pivotal in driving site activation, regulatory compliance, and clinical delivery in alignment with global sponsor expectations.

Key Responsibilities:

• Lead clinical operations and site-level engagement for assigned Phase’s studies in India
• Manage relationships with Principal Investigators (PIs), CRCs, and Institutional stakeholders at government hospitals
• Oversee timely and compliant PSSV, site initiation visits (SIV), patient recruitment, and data collection
• Ensure study milestones are met, including First Patient First Visit (FPFV) and clean database targets
• Collaborate with sponsor teams, regulatory consultants, and third-party vendors to streamline dossier submissions and audit readiness
• Coordinate regulatory submissions and ethics committee (EC) approvals; ensure alignment with CDSCO, ICMR, and local EC timelines
• Conduct ongoing risk assessment and drive mitigation strategies across sites
• Provide oversight to field CRAs and monitor site compliance
• Contribute to internal SOP development and quality initiatives

Key Qualifications:

• Bachelor’s degree in life sciences or related field; advanced degree preferred
• Minimum 6-8 years of clinical research experience with at least 3 years in an independent CTM role
• Demonstrated experience in oncology or immunotherapy trials, preferably with exposure to AIIMS or government research centers
• Strong working knowledge of GCP, ICH, and CDSCO guidelines
• Proven track record managing multi-site studies and remote monitoring teams
• Excellent interpersonal, communication, and problem-solving skills
• Proficiency in CTMS, EDC, and eTMF systems is a plus

Job Title: Clinical Trial Manager

Onsite - Hyderabad

Company Overview: We eteraflex connects a fast-growing global CRO specializing in oncology, rare diseases, and immunotherapies. Our mission is to accelerate access to innovative treatments by combining regulatory precision with deep site engagement, particularly in complex government-led research environments across India.

Position Summary: We are seeking an experienced Clinical Trial Manager (CTM) to lead the execution of Phase I, II and III oncology studies at key national institutions in India. This role is pivotal in driving site activation, regulatory compliance, and clinical delivery in alignment with global sponsor expectations.

Key Responsibilities:

• Lead clinical operations and site-level engagement for assigned Phase’s studies in India
• Manage relationships with Principal Investigators (PIs), CRCs, and Institutional stakeholders at government hospitals
• Oversee timely and compliant PSSV, site initiation visits (SIV), patient recruitment, and data collection
• Ensure study milestones are met, including First Patient First Visit (FPFV) and clean database targets
• Collaborate with sponsor teams, regulatory consultants, and third-party vendors to streamline dossier submissions and audit readiness
• Coordinate regulatory submissions and ethics committee (EC) approvals;
  ensure alignment with CDSCO, ICMR, and local EC timelines
• Conduct ongoing risk assessment and drive mitigation strategies across sites
• Provide oversight to field CRAs and monitor site compliance
• Contribute to internal SOP development and quality initiatives

Key Qualifications:

• Bachelor’s degree in life sciences or related field;
  advanced degree preferred
• Minimum 6-8 years of clinical research experience with at least 3 years in an independent CTM role
• Demonstrated experience in oncology or immunotherapy trials, preferably with exposure to AIIMS or government research centers
• Strong working knowledge of GCP, ICH, and CDSCO guidelines
• Proven track record managing multi-site studies and remote monitoring teams
• Excellent interpersonal, communication, and problem-solving skills
• Proficiency in CTMS, EDC, and eTMF systems is a plus