Clinical Trial Manager – CTM 

Precision for Medicine isn’t your typical CRO. We’re passionate about supporting your professional growth and career trajectory in nuclear medicine as a Clinical Trial Manager. If you have experience in radiopharmaceuticals, join our team as a Clinical Trial Manager and support cutting-edge companies bringing life-changing therapies to market ensuring patients have access to breakthrough treatments. You will serve as the clinical trial lead responsible for the planning, conduct, and oversight of the operational portion of clinical studies per defined scope of work to ensure clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

About You:

• You have a minimum of 5 years clinical research experience with significant clinical monitoring experience in radiopharmaceuticals and/or radiolabeling.
• You are knowledgeable about ICH-GCP, regulatory guidance and can implement working knowledge of clinical management techniques and tools.
• You are a leader with experience in functional management who excels at delegating while fostering cohesive team dynamics.
• You are results oriented, have a high level of integrity, and the ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency.

About the Role:

As the primary contact for clients, you will develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) and maintain good working relationships with investigators and the study team to ensure effective and timely feasibility, site start up, enrollment, maintenance, and close out procedures. As the CTM, you are responsible for generating potential site lists from key stakeholders, driving site feasibility process, and identifying potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment. As the leader of your team, you will lead internal team meetings and set team expectations with CRAs and CTAs, inspiring excellence and insisting the highest standards from a professional and ethical perspective.

Required:

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred 
• Minimum of 5 years of clinical research experience or proven competencies for the position
• Significant clinical monitoring experience in radiopharmaceuticals and/or radiolabeling
• Ability to travel domestically and internationally including overnight stays 

More about Us

Precision for Medicine is the first biomarker-driven clinical research and development services organization supporting life sciences companies in the use of biomarkers essential to targeting patient treatments more precisely and effectively. Precision applies a transformational approach to clinical research that integrates clinical trial design and execution with deep scientific knowledge, laboratory expertise, data intelligence and advanced manufacturing solutions. This convergence is driving faster clinical development and approval. Precision for Medicine is part of Precision Medicine Group, with 3,500 people in 40 locations globally across North America, Europe and Asia-Pacific. For more information, visit PrecisionForMedicine.com.