Clinical Affairs Specialist
Abbott
Clinical Affairs Specialist
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
Associates Degree (± 13 years)
Experience/Background
Minimum 1 year
Locations
- Tokyo, Tokyo, Japan
Salary
75,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical trials managementintermediate
- Data collection and reportingintermediate
- Adverse event monitoringintermediate
- Regulatory reportingintermediate
- Investigator recruitment and negotiationintermediate
Required Qualifications
- Associates Degree (±13 years) (experience)
- Minimum 1 year experience (experience)
Responsibilities
- Oversee direction, planning, execution of clinical trials/research
- Contribute to implementation of 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 for regulatory agencies
- Monitor protocol adherence and study completion
- Coordinate investigator initiations and group studies
Answer 10 quick questions to check your fit for Clinical Affairs Specialist @ Abbott.
Related Books and Jobs
Clinical Affairs Specialist
Abbott
Clinical Affairs Specialist
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
Associates Degree (± 13 years)
Experience/Background
Minimum 1 year
Locations
- Tokyo, Tokyo, Japan
Salary
75,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical trials managementintermediate
- Data collection and reportingintermediate
- Adverse event monitoringintermediate
- Regulatory reportingintermediate
- Investigator recruitment and negotiationintermediate
Required Qualifications
- Associates Degree (±13 years) (experience)
- Minimum 1 year experience (experience)
Responsibilities
- Oversee direction, planning, execution of clinical trials/research
- Contribute to implementation of 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 for regulatory agencies
- Monitor protocol adherence and study completion
- Coordinate investigator initiations and group studies
Answer 10 quick questions to check your fit for Clinical Affairs Specialist @ Abbott.
Related Books and Jobs