PL - Associate Director, Clinical Research
Verona Pharma
This listing was originally posted on Verona Pharma's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Project lead for GYN programs.
Our Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct innovative clinical research thus broaden the indications and facilitate the drug development globally. This individual will be the key driver of assigned program(s) for developing products towards registration, with efforts on developing study protocol, engaging key opinion leaders, drafting study report, and preparing dossier for regulatory submission.
Requirement:
A PHD/Master in clinical medicine (at least 5-year medical school graduates) with postgraduate training in oncology or relative major.
Deep understanding of China regulatory environment and clinical development procedure.
Previous experience of clinical research/clinical development is highly desirable, including strategy development, medical monitoring, and protocol/ writing.
The candidate who is ideally suited for this position will 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).
The position may require the flexibility to work outside of the area of primary medical specialization.
Required Skills:
Adaptability, Clinical Quality Management, Clinical Research, Clinical Study Design, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Data Analysis, Healthcare Project Management, ICH GCP Guidelines, Investigation Procedures, IS Audit, Medical Research, Medical Writing, Process Improvements, Recruiting, Regulatory Compliance, Risk Management, Strategic Planning, Strategic Thinking, Team Leadership, Training and DevelopmentPreferred Skills:
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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:
06/30/2026*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.
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