343 Clinical Trial Manager jobs in India

• Developing and managing clinical trial budgets and timelines.
• Selecting and managing clinical sites and investigators.
• Overseeing study start-up activities, including regulatory submissions and essential document collection.
• Monitoring trial progress, ensuring data integrity, and managing adverse events reporting.
• Collaborating with cross-functional teams, including data management, biostatistics, and medical affairs.
• Developing and implementing risk mitigation strategies for clinical trials.
• Ensuring timely closure of clinical trials and final report generation.
• Maintaining effective communication with investigators, study coordinators, and internal stakeholders.
• Mentoring and providing guidance to clinical research associates (CRAs) and other study team members.
• Troubleshooting and resolving issues that arise during trial conduct.

• Manage all aspects of clinical trials from planning and initiation to execution and closure, ensuring adherence to protocol, GCP, and regulatory guidelines.
• Develop and manage clinical trial budgets, timelines, and resources.
• Select, train, and manage investigational sites and clinical research organizations (CROs).
• Oversee the activities of Clinical Research Associates (CRAs) and other site personnel.
• Ensure data quality and integrity through regular monitoring and review of study data.
• Prepare and present study progress reports to internal stakeholders and regulatory authorities.
• Manage communication with investigators, study coordinators, and study sponsors.
• Identify and mitigate risks associated with clinical trial execution.
• Contribute to the development of study protocols, case report forms (CRFs), and other trial-related documents.
• Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH-GCP).
• Collaborate with internal departments, including regulatory affairs, medical affairs, and biostatistics.
• Plan and conduct site initiation visits, interim monitoring visits, and close-out visits.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
• Minimum of 5-7 years of experience in clinical trial management, with at least 3 years specifically in oncology trials.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in managing multiple clinical trials simultaneously.
• Strong project management skills, including planning, execution, and risk management.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to investigational sites as needed.
• Strong analytical and problem-solving abilities.
• Experience working with CROs and other vendors.
• Ability to work effectively in a hybrid work environment.

• Plan, manage, and execute clinical trials in compliance with protocols and regulations.
• Develop and finalize clinical trial protocols, informed consent forms, and other study documents.
• Identify, evaluate, and select clinical trial sites and investigators.
• Provide training and ongoing support to clinical site staff.
• Monitor clinical trial progress, data quality, and subject safety.
• Manage study budgets and resources effectively.
• Ensure compliance with Good Clinical Practice (GCP) and other relevant guidelines.
• Liaise with regulatory authorities and prepare submission documents.
• Oversee vendor activities and performance.
• Troubleshoot and resolve operational issues that arise during the trial.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
• Minimum of 5 years of experience in clinical trial management within the pharmaceutical industry.
• In-depth knowledge of clinical trial phases, methodologies, and regulatory requirements.
• Proven experience in site selection, monitoring, and management.
• Strong project management skills, including budgeting and timeline management.
• Excellent understanding of GCP, FDA, ICH guidelines, and other relevant regulations.
• Exceptional communication, leadership, and interpersonal skills for remote team collaboration.
• Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and manage complex projects in a remote environment.

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

Awards

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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