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Job Description
- Responsible for implementing general strategy and plans of the medical department, dividing them into objectives and reporting for the results.
- Duties and Responsibilities:
- Ensuring the proper application of good clinical practice (GCP/ICH) guidelines in the study;
starting from protocol approval by ethics committee, safety delivering and storage of the drugs
(accountability), reporting adverse events (serious and non-serious) and patients’ consents. - Regular contact with the investigators to ensure strict application of the study protocol,
documentation and CRFs proper completion. - Collecting CRF and study reports from different centers participating in the study.
Job Requirements
- Bachelor’s degree in a medical field.
- Computer skills: Office & internet surfing
- English language: very good written & spoken.
- Skills and Attributes:
- Strong communication and public presentation skills
- Excellent interpersonal skills with the ability to interact with physicians and researchers across
The health system. - Strong ability to handle multiple programs and portfolios.
- Ability to work both independently and as part of a team.