Description
Requirements of the role:- Medically manages clinical trials to which you are assigned as medical monitor. Collaborates with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)
- Provides therapeutic and protocol-specific training to the project teams
- Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc
- Maintains working knowledge of GCPs and regulatory requirements relating to clinical development and safety assure compliance with ethical, legal and regulatory standards
- Assists in the mentoring of other medical staff (nurses, junior physicians, etc) as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, support Senior Management's leadership of both the department and the company
- Provides after hours medical support for projects to which you are assigned
- Supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management
- Reviews and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc.) as directed by senior management
Among other Duties.
The Ideal Candidate will have the following requirements:
- Medical Degree from an accredited institution of Medical Education.
- Two years clinical research or industry experience
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Excellent computer skills (Word, Excel, Access)
Excellent organizational and time management skills -
Excellent communication skills -
Excellent presentation skills
If you are interested please email your details to the address below and I will call to discuss further.