Regional Medical Advisor
Abbott
Regional Medical Advisor
Job Description
MAIN PURPOSE OF THE ROLE
Experienced professional individual contributor that works under limited supervision.
Applies subject matter knowledge in the area of Medical Affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
MAIN RESPONSIBILITIES
• As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills 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 1 year
Locations
- Mumbai, India
Salary
55,000 - 95,000 INR / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Medical Affairs expertiseintermediate
- clinical trials oversightintermediate
- clinical researchintermediate
- protocol implementationintermediate
- investigator recruitmentintermediate
- study design negotiationintermediate
- adverse event reportingintermediate
- safety monitoringintermediate
- regulatory reportingintermediate
Required Qualifications
- Associates Degree (± 13 years) (experience)
- Minimum 1 year experience (experience)
Responsibilities
- Oversee direction, planning, execution, clinical trials/research and data collection activities
- Contribute to implementation of clinical protocols and facilitate completion of final reports
- Recruit clinical investigators and negotiate study design and costs
- Direct human clinical trials phases III & IV
- Participate in adverse event reporting and safety responsibilities monitoring
- Coordinate and provide reporting information for regulatory agencies
- Monitor adherence to protocols and determine study completion
- Coordinate investigator initiations and group studies
- Act as consultant/liaison with other corporations under licensing agreements
Answer 10 quick questions to check your fit for Regional Medical Advisor @ Abbott.
Regional Medical Advisor
Abbott
Regional Medical Advisor
Job Description
MAIN PURPOSE OF THE ROLE
Experienced professional individual contributor that works under limited supervision.
Applies subject matter knowledge in the area of Medical Affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
MAIN RESPONSIBILITIES
• As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills 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 1 year
Locations
- Mumbai, India
Salary
55,000 - 95,000 INR / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Medical Affairs expertiseintermediate
- clinical trials oversightintermediate
- clinical researchintermediate
- protocol implementationintermediate
- investigator recruitmentintermediate
- study design negotiationintermediate
- adverse event reportingintermediate
- safety monitoringintermediate
- regulatory reportingintermediate
Required Qualifications
- Associates Degree (± 13 years) (experience)
- Minimum 1 year experience (experience)
Responsibilities
- Oversee direction, planning, execution, clinical trials/research and data collection activities
- Contribute to implementation of clinical protocols and facilitate completion of final reports
- Recruit clinical investigators and negotiate study design and costs
- Direct human clinical trials phases III & IV
- Participate in adverse event reporting and safety responsibilities monitoring
- Coordinate and provide reporting information for regulatory agencies
- Monitor adherence to protocols and determine study completion
- Coordinate investigator initiations and group studies
- Act as consultant/liaison with other corporations under licensing agreements
Answer 10 quick questions to check your fit for Regional Medical Advisor @ Abbott.