Provides leadership to the global medical function including medical monitoring. Collaborates with
Global Medical Affairs Leadership on the ongoing development of the Department and contributes to the
business plan at both the tactical and strategic levels. Directly and through subordinate staff ensures the
successful management of medical advisory and medical monitoring projects in compliance with federal
regulations ICH Guidelines Good Clinical Practices (GCPs) and the Companys Standard Operating
Procedures (SOPs). Additionally this position involves cross-functional communications strategic
planning and participation in clients strategic decision-making physician review medical monitoring
and critical interactions with scientific advisors.
The Medical Director will assist the Head of Medical Affairs in educating mentoring and developing
Ergomed physicians to ensure their competence and confidence in developing their skills to become
subject matter experts in medical monitoring. The role requires active monitoring of costs and project
deliverables and interaction with the project managers project directors and the Head of Medical
Affairs. Additionally the role must include the review and implementation of efficiency strategies whilst
maintaining the highest quality of work.
ROLE AND RESPONSIBILITIES
- Provides all levels of medical monitoring activities including patient safety surveillance and integrity.
- Included in multi-cross-functional support to the project team in conducting clinical trials
- Could act as the main point of contact with the sponsor as a medical representative
- Coordination and delivery of trainings supervision and oversight of Medical Monitors
- Main point of contact and escalation for Medical Monitors
- Participation in the development and revision of Medical Monitoring SOPs
- Assists with the assignment transitioning and assimilation of individuals to work as Medical Advisors Medical Monitors and Study Physicians on project.
- Interacts with other departments to ensure the required quality of service is provided to a sponsor
Qualifications :
QUALIFICATIONS
Proven efficient medical communication
Highly organized with strong interpersonal presentational and documentation skills
Proven efficiency in timely delivery
Self-motivated able to work independently as well as in multi-disciplinary teams and with the intellectual flexibility to continually develop and learn new skills
In-depth knowledge of medical terminology and of GCP ICH guidelines relevant to global drug safety and drug development process and regulations
Good decision-making and problem resolution based on all relevant information.
Strategic thinking recognizing key issues and providing practical solutions
Ability to work effectively in an environment characterized by tight timelines and changing priorities.
Excellent Leadership skills
Additional Information :
Why Should You Apply
- You want be involved in a wide range of interesting projects and studies
- You want your achievements and hard work to be recognized
- You want to work for a growing company where you can progress in your career and where there are opportunities for advancement.
- You want to work in a company that has a great reputation with its clients and employees and invests in its relationships with both
All your information will be kept confidential according to EEO guidelines.
Remote Work :
Yes
Employment Type :
Full-time
Provides leadership to the global medical function including medical monitoring. Collaborates withGlobal Medical Affairs Leadership on the ongoing development of the Department and contributes to thebusiness plan at both the tactical and strategic levels. Directly and through subordinate staff ensur...
Provides leadership to the global medical function including medical monitoring. Collaborates with
Global Medical Affairs Leadership on the ongoing development of the Department and contributes to the
business plan at both the tactical and strategic levels. Directly and through subordinate staff ensures the
successful management of medical advisory and medical monitoring projects in compliance with federal
regulations ICH Guidelines Good Clinical Practices (GCPs) and the Companys Standard Operating
Procedures (SOPs). Additionally this position involves cross-functional communications strategic
planning and participation in clients strategic decision-making physician review medical monitoring
and critical interactions with scientific advisors.
The Medical Director will assist the Head of Medical Affairs in educating mentoring and developing
Ergomed physicians to ensure their competence and confidence in developing their skills to become
subject matter experts in medical monitoring. The role requires active monitoring of costs and project
deliverables and interaction with the project managers project directors and the Head of Medical
Affairs. Additionally the role must include the review and implementation of efficiency strategies whilst
maintaining the highest quality of work.
ROLE AND RESPONSIBILITIES
- Provides all levels of medical monitoring activities including patient safety surveillance and integrity.
- Included in multi-cross-functional support to the project team in conducting clinical trials
- Could act as the main point of contact with the sponsor as a medical representative
- Coordination and delivery of trainings supervision and oversight of Medical Monitors
- Main point of contact and escalation for Medical Monitors
- Participation in the development and revision of Medical Monitoring SOPs
- Assists with the assignment transitioning and assimilation of individuals to work as Medical Advisors Medical Monitors and Study Physicians on project.
- Interacts with other departments to ensure the required quality of service is provided to a sponsor
Qualifications :
QUALIFICATIONS
Proven efficient medical communication
Highly organized with strong interpersonal presentational and documentation skills
Proven efficiency in timely delivery
Self-motivated able to work independently as well as in multi-disciplinary teams and with the intellectual flexibility to continually develop and learn new skills
In-depth knowledge of medical terminology and of GCP ICH guidelines relevant to global drug safety and drug development process and regulations
Good decision-making and problem resolution based on all relevant information.
Strategic thinking recognizing key issues and providing practical solutions
Ability to work effectively in an environment characterized by tight timelines and changing priorities.
Excellent Leadership skills
Additional Information :
Why Should You Apply
- You want be involved in a wide range of interesting projects and studies
- You want your achievements and hard work to be recognized
- You want to work for a growing company where you can progress in your career and where there are opportunities for advancement.
- You want to work in a company that has a great reputation with its clients and employees and invests in its relationships with both
All your information will be kept confidential according to EEO guidelines.
Remote Work :
Yes
Employment Type :
Full-time
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