Job Description
Title: Executive, Medical Affairs
Company Name: US FDA Approved Leading Pharmaceuticals Company
Vacancy: --
Age: at most 32 years
Location: Dhaka
Salary: Negotiable
Published: 23 Jun 2025
Education:
∎ Bachelor of Medicine and Bachelor of Surgery(MBBS)
∎ MBBS from a recognized institute with BMDC Registration.
∎ Additional MPH Degrees from any reputed university will be preferred.
∎ MBBS from a recognized institute with BMDC Registration.
∎ Additional MPH Degrees from any reputed university will be preferred.
Requirements:
Additional Requirements:
∎ Age at most 32 years
∎ Must have computer proficiency in SPSS and Microsoft Office (Excel, PowerPoint, and Word).
Responsibilities & Context:
∎ Develop a concept note, select investigators, study site, conduct feasibility, initiation, and monitoring of the study.
∎ Monitor study sites to ensure compliance with approved protocols and regulatory standards.
∎ Ensure proper documentation, data collection, and reporting procedures are followed.
∎ Communicate effectively with investigators, site staff, and project teams.
∎ Support ethics committee submissions and regulatory applications.
∎ Review and verify case report forms (CRFs) against source documents.
∎ Maintain accurate records of monitoring visits and study progress.
∎ Collaborate with cross-functional teams including data management, regulatory affairs, and pharmacovigilance.
∎ Facilitate the planning and implementation of scientific and medical initiatives that are consistent with the company's overarching strategic objectives.
∎ Foster a productive, efficient, and health-oriented relationship between medical and marketing teams, ensuring that communication encompasses various forms, ranging from monthly product planning and update meetings to informal daily interactions.
∎ Establish, cultivate, and sustain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) while organizing advanced educational forums in collaboration with them.
∎ Develop a concept note, select investigators, study site, conduct feasibility, initiation, and monitoring of the study.
∎ Monitor study sites to ensure compliance with approved protocols and regulatory standards.
∎ Ensure proper documentation, data collection, and reporting procedures are followed.
∎ Communicate effectively with investigators, site staff, and project teams.
∎ Support ethics committee submissions and regulatory applications.
∎ Review and verify case report forms (CRFs) against source documents.
∎ Maintain accurate records of monitoring visits and study progress.
∎ Collaborate with cross-functional teams including data management, regulatory affairs, and pharmacovigilance.
∎ Facilitate the planning and implementation of scientific and medical initiatives that are consistent with the company's overarching strategic objectives.
∎ Foster a productive, efficient, and health-oriented relationship between medical and marketing teams, ensuring that communication encompasses various forms, ranging from monthly product planning and update meetings to informal daily interactions.
∎ Establish, cultivate, and sustain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) while organizing advanced educational forums in collaboration with them.
Workplace:
∎ Work at office
Employment Status: Full Time
Job Location: Dhaka
Company Information:
∎ US FDA Approved Leading Pharmaceuticals Company
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Application Deadline: 3 Jul 2025
Category: Others
