Clinician/Clinician Manager

🕒 June 2

🇨🇳 China – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 45%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Provides clinical and scientific expertise to the clinical trial strategy and protocol development process, including acquisition of knowledge of competitor products. • Designs/writes clinical trial outlines, protocols and amendments, in collaboration with internal contributors and external experts. • Creates (and where appropriate, delivers) clinical/protocol training materials for study and site management. • Helps establish and oversees Data Monitoring Committees (DMCs) and endpoint adjudication committees. • Maintains direct contact with investigative sites to facilitate investigator engagement and support enrolment activities.

🎯 Requirements

• Fluent in both oral and written English • Fluent in host country language required • Thorough understanding of local / international regulations applicable to clinical trials (pre and post approval). • Practical experience in clinical trial strategies, methods and processes. • Track record of design, oversight and interpretation of clinical studies. • Previous leadership /management experience or training. • Knowledge and experience in Good Clinical Practices.

🏖️ Benefits

• Health insurance • Flexible work arrangements