Manager, Clinical Research
MSD
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Main Responsibility
- The clinical research physician is expected to abstract high level relevant clinical and preclinical data and effectively use these data in supporting China registration. The clinical research physician is expected to address issues/questions raised.
- Whenever Clinical Research designs a clinical study, the clinical research physician (clinical monitor) is expected to drive study design, and collaborate with biostatisticians, regulatory affairs, and other relevant disciplines to construct a high quality clinical study protocol.
- The clinical research physician will also work as clinical scientist, to lead lab selection and clinical supply application during study planning phase, provide scientific inputs, and review protocol deviation and answer protocol related questions during study implementation phase.
- To develop the best, most suitable clinical plan and protocol, the clinical research physician is expected to engage scientific leaders and internal key stakeholders such as medical affair, and marketing and regulatory affair.
- The clinical research physician will participate due diligence evaluation as expert for medical related matter. Clinical physician is also working closely with medical affair to identify gap/opportunities of patient care in China and develop clinical plan/study to capitalize the emerging opportunities.
Requirements
- Master Degree and above in clinical medicine (at least 5 year medical school graduates)
- Deep understanding of China regulatory environment and clinical development procedure.
- Previous experience of clinical research/clinical development is highly desirable.
- Be bright, driven, dedicated, persistent, strategic, flexible, clever, and resourceful.
- The candidate should have a strong leadership, excellent written and oral communication skills, and project management skills.
- Strong capability of work prioritization and deliver results with parallel multiple tasks.
- Excellent language skills in both English and Chinese (fluent in verbal and written).
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Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
07/31/2024*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Job Posting End Date:07/31/2024
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R292146
This job is no longer accepting applications
See open jobs at MSD.See open jobs similar to "Manager, Clinical Research" LHH.