Medical Director | China

Medical Director | China

inVentiv Health Clinical SRE, LLC
Not Specified
Not Specified

Job Description

Job Description :

Interacts with senior management, customers, and project teams to ensure the safety of subjects in clinical trials;
ensures the scientific integrity of the clinical portions of clinical trials; provides medical input to clinical programs;
provides clinical development and regulatory consulting advice as needed. Performs the duties of a Medical
Monitor. Manages subordinate physicians when required to do so.
Essential Functions:
1. Responsible for subject-safety and the scientific integrity of clinical trials.
2. Performs the duties of a Medical Monitor.
3. Provides 24-hour coverage for clinical trials.
4. Participates in bids, bid-defenses & feasibility assessments when requested.
5. Provides project-specific and therapeutic training to sponsors and Company staff as needed.
6. Works with the Drug Safety Department by providing medical input and oversight.
7. Works with Medical Writing/Regulatory in the preparation of a variety of documents as required.
8. Maintains in-depth knowledge of worldwide drug development regulations and Good Clinical Practice (GCP)
9. Interacts with senior management, project management and other departments as appropriate.
10. Provides clinical development and regulatory consulting advice both within Company and to clients as
11. Locates and interacts with outside experts as necessary.
12. Provides feedback to management on quality issues within the clinical trial team
13. Represents Company at scientific meetings as required
14. Primary senior-level contact for customers.
15. Assumes line-management duties as needed. Qualifications

A doctoral-level degree in medicine and must have practiced medicine and have extensive clinical research
experience. In-depth knowledge of FDA and worldwide drug-development regulations. Strong understanding of
the use of medical terminology and of drug-names in multiple nations, cultures and environments. In-depth
knowledge of national and ICH Good Clinical Practice (GCP) guidelines. Basic computer and word-processing
skills, including the use of spreadsheets, e-mails and smart-phones. Experience working in matrix-teams. Ability to
handle multiple tasks to meet deadlines in a dynamic environment. Effective organizational and interpersonal skills.
Skilled at presenting data to groups, and in the creation of effective documentary communication. Customerfocused
with a disciplined approach to work with excellent verbal communication and language skills. Fluency in
written and spoken English.

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