Opportunity for M.Pharm as Clinical Research Specialist at Dr. Reddy’s Laboratories
Post : Clinical Research Specialist
Job Description
Purpose
Execute, manage and oversee the clinical trial operations activities for both in-house and outsourced studies for optimal clinical development of global generic formulations and differentiated products
• Particulars
• Planning and execution of clinical studies, monitoring and conducting the clinical development operation activities of clinical and patient based pharmacokinetic studies
• Identification, technical evaluation and monitoring the CRO/ vendor activities
• Develop/ improve Clinical Operations systems/ procedures
• Prepare / review clinical study documents
• Preparation/ review of clinical study reports
• Have a broad understanding of the Clinical operations methodology, Clinical trial management, Regulatory requirements for late phase clinical and Pharmacokinetic studies
Candidate Profile
MPharm (Pharmacology)/ PG in life-sciences with 6-10 years of experience in clinical monitoring of patient based studies
Additional Information
Experience : 6 to 10 Years
Qualification : M.Pharm
Location : Bachupally, Hyderabad, Telangana, India
Skills Required : Clinical Monitoring, Project Management, Communication, Presentation
End Date : 15th August, 2020.
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube