Remote opportunity at
Precision Medicine GroupClinical Trial Manager/Senior Clinical Trial Manager
Precision Medicine Group seeks a Clinical Trial Manager or Senior Clinical Trial Manager to lead the operational planning, execution, and oversight of clinical studies. This full-time…
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About This Role
Precision Medicine Group seeks a Clinical Trial Manager or Senior Clinical Trial Manager to lead the operational planning, execution, and oversight of clinical studies. This full-time position operates remotely and offers a salary between USD 110,700 and 200,900 per year. The person in this role will serve as the main clinical point of contact for clients, direct internal clinical team meetings, manage site feasibility and recruitment strategies, and oversee regulatory…
Job Description
Precision Medicine Group seeks a Clinical Trial Manager or Senior Clinical Trial Manager to lead the operational planning, execution, and oversight of clinical studies. This full-time position operates remotely and offers a salary between USD 110,700 and 200,900 per year.
The person in this role will serve as the main clinical point of contact for clients, direct internal clinical team meetings, manage site feasibility and recruitment strategies, and oversee regulatory submissions alongside institutional review boards and competent authorities. Additional duties include eTMF administration, investigational product management, monitoring plan execution, and handling vendor relations for laboratories and patient diaries.
This role suits professionals with extensive clinical research expertise, strong capabilities in cross-functional team environments, and knowledge of regulatory guidelines. Candidates must possess the ability to travel both domestically and internationally, including overnight stays.
Responsibilities
- Act as the primary clinical point of contact for clients
- Collaborate on monthly invoicing and clinical budget variance management
- Create study-related documents such as clinical plans, informed consent templates, manuals, and tracking tools
- Identify CRA and third-party vendor training needs and present at kickoff meetings
- Drive site feasibility processes and establish country recruitment and retention strategies
- Lead internal clinical team meetings and maintain communication with investigators and study teams
- Oversee and track submissions and approvals to competent authorities and ethics committees
- Implement and manage the eTMF and ensure data quality and cleaning compliance
- Develop and close corrective and preventative action plans in collaboration with quality assurance and project management
- Manage investigational product processes, drug accountability, and reconciliation
Requirements
- Minimum of seven years of clinical research experience or proven competencies with substantial clinical monitoring experience
- Proficiency with Microsoft Office applications including Outlook, Word, Excel, and PowerPoint
- Demonstrated mastery knowledge of ICH-GCP, relevant standard operating procedures, and regulatory guidance
- Direct work background in cross-functional settings
- Proven background in functional management, planning, risk management, and change management
- In-depth proven experience in pharmaceutical and/or device research
- Ability to travel domestically and internationally with overnight stays
- Legal authorization to work in the country of employment without employer sponsorship
Qualifications
- Bachelor's degree or equivalent combination of education and experience in a science or health-related field
- Advanced degree in a science or health-related field
Core Skills
Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance
- Disability benefits
- Parental leave
- Paid time off for sick leave and vacation
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
What is the salary range for this role?
The compensation range is estimated between USD 110,700 and 200,900 per year, and the role is also eligible for a discretionary annual bonus and other benefits.
Is this position remote?
Yes, the posting specifies that the role is remote, though it requires the ability to travel domestically and internationally including overnight stays.
What educational background is required?
Candidates must have a bachelor's degree or an equivalent combination of education and experience in a science or health-related field, while an advanced degree is preferred.
Are candidates required to have prior clinical research experience?
Yes, applicants need a minimum of 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring background, alongside in-depth proven experience in pharmaceutical or device research.
Sample Interview Questions
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