Remote Clinical Project Manager

Clinical Project Manager | Mid-Sized CRO | Homebased/Remote USA



Remote USA




Clinical Research

i-Pharm Consulting has partnered with a mid-sized CRO seeking a Sr. Clinical Project Manager for a home-based role in the US. Our client is searching for candidates with at least three (3) years of project management and CRO experience. Candidates that wish to pioneer the way therapies are developed and delivered are strongly encouraged to apply.

Location : USA, Home-based, Remote

The Role

Acting as the Clinical Project Manager, you will become the primary liaison between the sponsor and the vendor. The CPM is responsible for end-to-end clinical trial execution through coordination of colleagues, information and tools to ensure trial success. Throughout the entire process, CPMs will evaluate project progress through maintenance proper timelines and financial information.

Documentation control with regulatory affairs will be vital along the project timeline to ensure audit compliance. CPMs will prepare study material and present content at client meetings. One must regularly attend staff meetings, team meetings and clinical training sessions to monitor project communication. As potential concerns arise, you must alert senior management to ensure corrective action to take place.

Being able to establish, develop and maintain strong relationships with current clients will assist the business development team to grow their book for the future. One must be comfortable presenting proposals, capability statements, patient populations, etc. to customers in defence meetings.

Other work-related duties may be assigned such as representing the company at professional meetings and/or seminars.

Therapeutic areas include, but are not limited to: CNS | Neurology | Dermatology | HIV | Infectious Disease | Respiratory | Anti-Bacterials | HEP B | Allergies | Oncology

Minimum travel percentage: 20 – 30%


Regular employees working over 30 hours per week remain eligible for benefits (health, dental, vision, life, disability). The benefit package begins on the first day of the month following the hire date. Disability benefits begin 90 days following the fire date. All employees, regardless of full-time or part-time are entitled to 401(k) benefits. Paid holidays include: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving Day + Day After, Christmas Day, December 26th – Jan 1st.

Experience Required

BS/BA in life sciences, nursing or equivalent combination of education and experience. Moderate to advanced experience in clinical research within a CRO, pharmaceutical or biotechnology company.Prior experience in conducting multiple global, national or local clinical trials within a CRO, pharma or hospital setting. Candidate must have spent time managing clinical projects across various functional areas. Thorough knowledge of regulatory body requirements, project development and clinical monitoring.Proficiency with ICH/GCP guidelines.Takes a team-oriented approach to project management.Proficiency in Microsoft 365.Ability to mentor/manage new staff, encouraging all teams to reach deadlines while maintaining high quality work.

Note: If your application does not meet the requirements, a rejection will not take place due to a high volume of applicants. Thank you!


If you would like to discuss this vacancy further, please call Sam Greer on +1 646 876 4889, or email [email protected] If this role is not suitable, Sam is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the USA, UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
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