Senior Research AssociateJobs Opening in Cadila Pharmaceuticals Ltd at Dholka
FEATURED JOBSenior Research Associate
Cadila Pharmaceuticals Ltd
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Posted: 17 Dec 25
Job Description
The major purpose of a Clinical Research Associate (CRA) is to ensure that clinical trials to be
conducted in compliance with regulatory requirements, ethical standards, GCP and the study
protocol.
Responsibilities:
- Acts as point of contact for communication between the team and external parties if any (i.e.
sponsor, central lab, PI)
- Charting of Site Initiation, Monitoring Plan
- Coordinate and distribute clinical study material to study sites
- Providing inputs for study protocol and CRF
- Coordinator with In-house/ Vendor/Pharmacist for IMP supply and shipments
- Supervise Clinical Research Activities
- Organize the IB, Protocol, CRF, ICF, Instruction manuals etc.
- Perform Site Identification and conduct feasibility studies
- Preparation and review of clinical trial related SOPs
- Presenting kick off meeting and project training to team members
- Perform projects SSV, SIV, SMV and SCV in timely manner
- Periodic monitoring to clinical trials sites
- Maintain updated site files and collection of essential documents
- Send follow up letter to sites and submit visit report to Project Manager
- Internal QC of study files/ documentation
- Archival of study documents
Regulatory & Ethical Affairs:
? Co-ordinate with sites for Ethics Committees Submission
? Updating about the trial status, such as investigator, site, SAE reporting and SCV
Job Particulars
Role research jrf srf
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2809614
Job Category Research
Locality Address
State
Country India
About Company
Cadila Pharmaceuticals Ltd
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