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Saturday, October 9, 2010

Sr Clinical Research Associate – Medical Writing

Summary

Experience:
0 - 2 Years
Location:
Pune
Compensation:
As per industry standard
Education:
UG - B.Pharma - Pharmacy,B.Sc - Any SpecializationPG - M.Pharma - Pharmacy
Industry Type:
Pharma/ Biotech/Clinical Research
Role:
Clinical Research Associate/Scientist
Functional Area:
Healthcare, Medical, R&D

Desired Candidate Profile

 • D Pharm, MPharm, B Sc with minimum 2 years of relevant experience in CRO / Hospitals.

Job Description

 • Writing of study protocols for Bioequivalence studies & Clinical end point studies as per ICH/GCP requirements.

• Coordinate with the Principal investigator, statistician and pharmacokineticist to elucidate study design and protocol development.

• Build procedures in compliance with established guidelines and regulatory requirements for BA/BE studies.

• Ensuring development of study reports that comply with ICH/GCP guidance.

• Contribute to an atmosphere of teamwork provide collaboration with external and internal clients.
Keywords: Clinical Research Associate, Medical Writing ,Protocol Writer, ICH / GCP, Bioequivalence ,

Company Profile

Synapse Labs is a Contract Research Organization (CRO) which offers a range of services to the Pharmaceutical and Biotechnology industry. We are dedicated to quality service, with focus on reducing time and cost, We are achieving this by understanding client requirement and working close with them to match their timeline. 

Synapse Labs offers services in Bioavailability/Bioequivalence Studies, Clinical Research (Phase II-IV), Data Management, Biometrics as well as formulation development and much more
Contact Details
Company Name:
Synapse Labs
Executive Name:
Pradnya Uplap
Address:
Not Mentioned

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