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Precision Medicine GroupClinical Trial Manager
Precision Medicine Group is hiring a Clinical Trial Manager to oversee the operational aspects of clinical studies. The organization combines advanced data sciences, laboratory expertise, and…
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About This Role
Precision Medicine Group is hiring a Clinical Trial Manager to oversee the operational aspects of clinical studies. The organization combines advanced data sciences, laboratory expertise, and scientific knowledge with clinical trial execution, maintaining a primary focus on rare disease and oncology research. In this remote, full-time position, the Clinical Trial Manager acts as the main clinical point of contact for clients and leads internal study teams. Responsibilities include managing study…
Job Description
Precision Medicine Group is hiring a Clinical Trial Manager to oversee the operational aspects of clinical studies. The organization combines advanced data sciences, laboratory expertise, and scientific knowledge with clinical trial execution, maintaining a primary focus on rare disease and oncology research.
In this remote, full-time position, the Clinical Trial Manager acts as the main clinical point of contact for clients and leads internal study teams. Responsibilities include managing study execution from start-up through close-out, guiding site feasibility, maintaining compliance with protocols and regulatory guidelines, and collaborating on budgeting and invoicing. This role requires domestic and international travel with overnight stays, as well as Mandarin language proficiency to support Mandarin-speaking clients.
This opportunity is ideal for clinical research professionals with substantial monitoring background and experience in healthy volunteer and Phase 1 first-in-human clinical trials. Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Responsibilities
- Act as the primary clinical point of contact for clients
- Collaborate on monthly invoicing and clinical budget variance management
- Create study-related documentation including clinical plans, informed consent form templates, manuals, and training materials
- Drive the site feasibility process and identify potential recruitment risks
- Establish country recruitment and retention strategies
- Lead internal clinical team meetings and direct clinical team expectations
- Oversee submissions and approvals involving Competent Authorities and IRBs or Ethics Committees
- Monitor study metrics using tools such as CTMS and data management query trends
- Implement and manage the eTMF
- Manage investigational product processes such as drug reconciliation and accountability
Requirements
- Minimum of 5 to 8 years of clinical research experience or proven competencies with substantial clinical monitoring background
- Experience with Phase 1 first-in-human and healthy volunteer clinical trials
- Mandarin language proficiency
- Familiarity with Microsoft Office products including Outlook, Word, Excel, and PowerPoint
- Legal authorization to work in the country of employment without employer sponsorship
- Ability to travel domestically and internationally with overnight stays
Qualifications
- Bachelor’s degree in a science or health-related field or equivalent combination of education and experience
- Advanced degree in a science or health-related field
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the posting specifies that the role is remote, though it does require the ability to travel domestically and internationally with overnight stays.
What is the employment type?
This is a full-time position.
What language skills are required?
Mandarin language proficiency is required to support Mandarin-speaking clients.
Does the posting specify a salary?
The salary is not stated in the job posting.
What education or experience is needed?
Candidates must have a bachelor's degree in a science or health-related field or equivalent education and experience, alongside 5 to 8 years of clinical research experience with significant monitoring background and Phase 1 FIH experience. An advanced degree is preferred.
Sample Interview Questions
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