Cipla Hiring For Clinical Operations Don’t Miss It

Job Posting: Team Member – Clinical Operations at Cipla

Company: Cipla
Location: Mumbai
Position: Team Member – Clinical Operations
Qualifications: B.Pharm, M.Pharm, MSc, BSc, MBBS, BVSC, MVSC
Experience: 2 Years
Salary: Not disclosed

About Cipla

Cipla operates within the Clinical Research field, focusing on executing studies to support regulatory submissions. This role is crucial in ensuring studies are conducted effectively and within regulatory guidelines, contributing to the advancement of pharmaceutical and chemical products.

Job Description

As a Team Member in Clinical Operations, you will execute, monitor, report, and interpret preclinical, clinical, and BABE (Bioequivalence) studies at CROs to support various regulatory submissions within targeted timelines, budgets, quality, and regulatory guidelines.

Responsibilities

Responsibilities
Gather preclinical/clinical/BABE study outline data for trials.
Evaluate CROs for capability and facilities.
Liaise with CROs and internal teams for study protocol preparation.
Ensure procurement and dispatch of samples and formulations.
Monitor ongoing studies for compliance with guidelines and timelines.
Act as project coordinator, aligning stakeholders.
Conduct toxicological reviews and derive exposure limits.

Qualifications

Education Qualification:

Field	Qualifications
BABE	B.Pharm/B.Sc.
Clinical	B.Pharm/M.Sc./M.B.B.S./B.V.Sc. & A.H.
Preclinical	M.V.Sc. (Pharmacology and Toxicology) desirable

Relevant Work Experience:

Experience	Details
BA/BE or Clinical Research	2 years with knowledge of regulatory guidelines
Preclinical Pharmacology	2 years including practical experience

How to Apply

Connect with us via LinkedIn or email for more information.

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