Bayer Walk In Interview 2023 .Bayer Notification full details below..Intrested and eligible candidates can attend Interview on scheduled time and venue.A growing and aging world population and the increasing strain on nature’s ecosystems are among the major challenges facing humanity. As one of the world’s leading companies in the fields of health and nutrition, we are able to play a key role in devising solutions to tackle these challenges. The COVID-19 crisis and Russia’s invasion of Ukraine have reminded us of the importance of health and nutrition and underlined our systemic relevance.
Vacancy details:
- Department: Medical Research Associate
- Qualification: Bsc/Msc/B.pharm/M.pharm/Lifescience graduate
- Experienced: 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.
Job Description: Greeting from Bayer !!!!!!!!!!
Important Details :
- Location: Maharashtra – Thane
- Post of date:29/07/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Fact to face Interview.
- Rounds of Interview: HR
YOUR TASKS AND RESPONSIBILITIES:
To be a key resource personnel in Medical Affairs concerning Phase IV and 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 regular meetings and conference calls with project management, operation team and other team members, regional and global teams as required.
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 the resolving the quality issues of outsourced studies.
To provide regular status updates to the project team and related business cross-functional teams.
WHO YOU ARE:
Qualification: Bsc/Msc/B.pharm/M.pharm/Lifescience graduate
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
