Clinical Project Assistant
SanofiÂ
Advertisement
Job Description
Location: Delhi, India
Job Requisition ID: Not Specified
Job Category: Clinical Research / Site Operations
Job Type: Full-Time (On-site, Contract)
About the Role
MS Clinical Research is seeking enthusiastic and motivated Clinical Research Coordinators (CRC) to join our expanding clinical team in Delhi. This position offers an exciting opportunity for fresh graduates with a background in life sciences, pharmacy, or clinical research training to gain hands-on experience in the management and conduct of clinical trials.
As a CRC, you will play a key role in ensuring the smooth execution of clinical studies, maintaining compliance with ICH-GCP guidelines, and supporting the integrity of research data. This role provides a strong foundation for building a rewarding career in clinical research.
Role & Responsibilities
- Conduct clinical trials in accordance with ICH-GCP guidelines and study protocols.
- Support study start-up activities and assist with site initiation visits (SIVs).
- Participate in subject recruitment, screening, and retention processes.
- Complete and maintain source documents, case report forms (CRFs), and study logs accurately.
- Compile and regularly update the Site Master File (SMF) and ensure compliance readiness.
- Manage Investigational Product (IP) handling, accountability, and documentation.
- Coordinate Ethics Committee submissions and maintain regulatory correspondence.
- Communicate study progress and updates with sponsors and monitor site activities.
- Prepare for and support monitoring visits, audits, and inspections.
- Perform other site-related or administrative responsibilities as assigned by management.
Educational Qualification
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field.
- Completed Clinical Research certification or course preferred.
Experience & Skills
- Freshers with relevant training or coursework in clinical research are encouraged to apply.
- Strong understanding of clinical trial processes and regulatory compliance requirements.
- Excellent organizational, communication, and documentation skills.
- Proficiency in Microsoft Office tools (Word, Excel, Outlook).
- Ability to work effectively in a team and manage multiple tasks with attention to detail.
Location
Delhi, India
Advertisement
Recent Jobs
Clinical Research Associate 1
AstraZenecaÂ
CTIS Administrator
Parexel
Clinical Research Associate (Level I, Level II & Sr. CRA)
Thermo Fisher Scientific
Associate Clinical Study Manager
Novartis
eClinical Coordinator
Medpace
Pharmacovigilance Services Associate
accenture
Associate – Regulatory Affairs
CLINCHOICE