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PHARMA JOBS POST > Join Insignia: Study Start-Up Specialist Wanted in Clinical Trials

Join Insignia: Study Start-Up Specialist Wanted in Clinical Trials

ARPITA
Last updated: May 16, 2025 7:23 pm
ARPITA 1 year ago
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Insignia Clinical Services (ICS) is a full-service Contract Research Organization (CRO) based in India, offering comprehensive clinical research and regulatory solutions to the pharmaceutical, biotechnology, medical device, cosmetics, and healthcare industries. With a team combining over 50 years of experience from pharmaceutical, clinical research, and regulatory backgrounds, ICS provides end-to-end support across the clinical development lifecycle.

HIRING NOW STUDY STARTUP SPECIALIST
IN CLINICAL TRIALS

Key Responsibilities:
Site Selection and Feasibility, Regulatory Approvals, Study Start-up Activities, Contract Negotiation, Budget Management, Documentation Management, Communication and Collaboration, Site Activation, Problem Solving, Data Management

Qualification: B.Pharma /Master’s degree in a related field (e.g., life sciences, healthcare).

Experience: Minimum Two years of experience specifically in Study Startup Activities in clinical trials, preferably in a CRO (Contract Research Organization).

Skills:
•Strong knowledge of GCP, ICH and regulatory guidelines.
•Excellent organizational, communication, and interpersonal skills
•Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) tools.
•Ability to work independently and as part of a team.
•Experience with site feasibility assessments, budget management and site initiation.

MAIL YOUR CV AT:
careers@insigniacs.com

Salary: As per Industry Norms Delhi, Office-Based, Full Time

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