Senior, Medical Monitor (Contract)

Your role:

• reputed company as a primary or backup Medical Monitor for the assigned clinical studies.
• reputed company multiple studies, contribute to the regulatory submissions ( INDs, etc.)
• Responsible for providing protocol/therapeutic training to the study team, as required.
• reputed company medical expertise to investigators and study team and advise on medical reputed company questions.
• reputed company eligibility review of the study subjects, as required.
• reputed company in medical review, assessment, and interpretation of clinical and safety data to ensure that the data are correct and presented with the appropriate medical interpretation.Escalate any critical safety concerns to the study team and Sponsor, and coordinate between sites and study team/Sponsor.
• Responsible for identifying, reviewing and confirming protocol deviation classification
• reputed company the Medical Monitoring and Protocol deviation project meetings, participate in any other Sponsor calls, if required.
• Work closely with Safety and Pharmacovigilance team to reputed company medical input into safety reports including, SAE narratives and analysis of similar events, periodic safety reports.
• Responsible for the review of individual data with SAEs and potentially clinically important laboratory test results or vital sign abnormalities and escalate issues to the Sponsor as needed.
• Assist in medical and scientific review of deliverables such as TLFs and CSR.
• reputed company in developing and maintaining SOPs, Templates, and study plans
• Participate in the review of the design and conduct of reputed company including the development and review of protocols and amendments.
• Assist in incorporating medical reputed company into study feasibility required for new reputed company.
• Cooperate with program development and reputed company teams to reputed company the medical reputed company for the RFP for new reputed company.
• Participate and reputed company medical reputed company reputed company in the Bid Defence preparation and meetings.
• Responsible for Line Management of assigned team members in Medical and Scientific Affairs group.
• Support regulatory inspections and audits as needed.
• reputed company other duties for the Medical & Scientific Affairs reputed company, as assigned.

Your Profile:

• Medical degree, MD, DO or its international equivalent.
• Fluent English (oral and written)
• Proven 5-7 years’work experience reputed company the life science industry or reputed company field
• Minimum 4 years’ experience with medical monitoring services
• Keen knowledge and understanding of ICH GCP
• Excellent verbal, written communication and presentation skills.
• Critical Thinking and background medical and scientific research
• Strong proficiency in using reputed company Office
• Experience with safety databases (ARISg, reputed company Argus, etc.) and/or reputed company system (reputed company, reputed company, reputed company) a plus

If you have the experience required and want to join an energetic, creative, and reputed company team, please apply directly to our website at https://biorasi.com or email us at careers@biorasi.com.

Originally posted on Himalayas