Senior Medical Affairs Manager
Abbott
Senior Medical Affairs Manager
Job Description
MAIN PURPOSE OF THE ROLE
Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs.
Ability to execute highly complex or specialized projects.
Adapts precedent and may make significant departures from traditional approaches to develop solutions.
MAIN RESPONSIBILITIES
• As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• Monitors adherence to protocols and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.
• May act as consultant/liaison with other corporations when working under licensing agreements.
QUALIFICATIONS
Education
Education Level Major/Field of Study or Equivalent
Associates Degree (± 13 years)
Experience/Background
Experience Experience Details
Minimum 7 years
Locations
- Bangkok, Bangkok, Thailand
Salary
100,000 - 160,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical trials managementintermediate
- Adverse event reportingintermediate
- Protocol adherence monitoringintermediate
- Regulatory reportingintermediate
- Investigator recruitmentintermediate
Required Qualifications
- Associates Degree (±13 years) (experience)
- Minimum 7 years experience (experience)
Responsibilities
- Oversee direction, planning, execution of clinical trials/research
- Contribute to clinical protocols and final reports
- Recruit clinical investigators and negotiate study design/costs
- Direct human clinical trials phases III & IV
- Participate in adverse event reporting and safety monitoring
- Coordinate reporting to regulatory agencies
- Monitor protocol adherence and study completion
Answer 10 quick questions to check your fit for Senior Medical Affairs Manager @ Abbott.
Senior Medical Affairs Manager
Abbott
Senior Medical Affairs Manager
Job Description
MAIN PURPOSE OF THE ROLE
Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs.
Ability to execute highly complex or specialized projects.
Adapts precedent and may make significant departures from traditional approaches to develop solutions.
MAIN RESPONSIBILITIES
• As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• Monitors adherence to protocols and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.
• May act as consultant/liaison with other corporations when working under licensing agreements.
QUALIFICATIONS
Education
Education Level Major/Field of Study or Equivalent
Associates Degree (± 13 years)
Experience/Background
Experience Experience Details
Minimum 7 years
Locations
- Bangkok, Bangkok, Thailand
Salary
100,000 - 160,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical trials managementintermediate
- Adverse event reportingintermediate
- Protocol adherence monitoringintermediate
- Regulatory reportingintermediate
- Investigator recruitmentintermediate
Required Qualifications
- Associates Degree (±13 years) (experience)
- Minimum 7 years experience (experience)
Responsibilities
- Oversee direction, planning, execution of clinical trials/research
- Contribute to clinical protocols and final reports
- Recruit clinical investigators and negotiate study design/costs
- Direct human clinical trials phases III & IV
- Participate in adverse event reporting and safety monitoring
- Coordinate reporting to regulatory agencies
- Monitor protocol adherence and study completion
Answer 10 quick questions to check your fit for Senior Medical Affairs Manager @ Abbott.