FEATURED JOB

Research Associate

Cadila Pharmaceuticals Ltd

0 Years

Not disclosed

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Posted: 08 Jul 26

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 Id2920660

Job Category Research

Locality Address

State Gujarat

Country India

About Company

Cadila Pharmaceuticals Ltd

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