Bayer Freshers Job Opening – Medical Research Associate
Bayer Job Opening 2020 official notification has been released. Pharmaceutical Sciences Educators can check out all of the relevant information with regards to the Job Post. Pharmacovigilance Job Opening 2020. Interested and eligible candidates may apply online. Check out all the details
Job Title: MEDICAL RESEARCH ASSOCIATE (MRA) – 6 MONTHS BAYER CONTRACT
Eligibility Criteria:
- B.Sc./M.Sc./B.Pharm/M.Pharm
- Relevant clinical research experience in a pharmaceutical company/CRO with a good understanding and experience in handling clinical studies in line with ICH-GCP guidelines
- Ability to work independently as well as in a team environment and to build productive work relationships both internally and externally
- Fluent in English with good presentation and written and verbal communication skills
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Medical Professional
Role: Intern
WHAT YOU DO:
- To be key resource personnel in Medical Affairs concerning Non-interventional study (NIS) activities across all business areas
- To coordinate all study activities like CRO selection, preparation of study documents for review, site selection and site feasibility, update relevant tracking systems on an ongoing basis, implement quality checks especially for outsourced studies and manage clinical trial oversight, manage study budget and required resources, site monitoring and quality review and archival. The major responsibility includes on-time and on-budget study completions in India
- To manage all operational and quality aspects of allocated studies in compliance with ICH GCP
- Responsible for the implementation and training of standardized processes within the study and according to organizational SOPs
- Development of essential studies as per the local requirements and creating the essential documents like protocol, ICF etc with coordination of global/local team
- Ensures that essential documents quality meets the expectations of Regulatory requirements in India and Bayer guidelines and SOPs
- To attend the regular conference calls with the project management, clinical operation team and other clinical team members
- To communicate regularly with all other related departments to ensure timelines, resources, interactions and quality are maintained
- To prepare and monitor clinical activity timelines and metrics
- To ensure regular project review, using tracking and management tools, implementing appropriate recovery actions to ensure project timelines are met
- Responsible for resolving the quality issues of outsourced studies
- To provide regular status updates to the project team and related business cross-functional teams
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