Medical Advisor
Abbott
Medical Advisor
Job Description
MAIN PURPOSE OF 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
Education Level
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 affairsintermediate
- clinical trials managementintermediate
- protocol implementationintermediate
- adverse event reportingintermediate
- 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
- Contribute to implementation of clinical protocols and facilitate 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 monitoring
- Coordinate reporting to regulatory agencies
- Monitor adherence to protocols and determine study completion
- Coordinate investigator initiations and group studies
- Act as consultant/liaison with other corporations
Answer 10 quick questions to check your fit for Medical Advisor @ Abbott.
Medical Advisor
Abbott
Medical Advisor
Job Description
MAIN PURPOSE OF 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
Education Level
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 affairsintermediate
- clinical trials managementintermediate
- protocol implementationintermediate
- adverse event reportingintermediate
- 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
- Contribute to implementation of clinical protocols and facilitate 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 monitoring
- Coordinate reporting to regulatory agencies
- Monitor adherence to protocols and determine study completion
- Coordinate investigator initiations and group studies
- Act as consultant/liaison with other corporations
Answer 10 quick questions to check your fit for Medical Advisor @ Abbott.