Provide leadership, local/global strategic planning and operational delivery of assigned clinical studies/program through all phases of study management (study start-up, conduct/maintenance, closure)
Ensure the effective identification, initiation and motivation (patient recruitment/retention) of clinical study sites
Focus on internal and external customers service (Sponsors, study sites, vendors) related to site management and clinical monitoring activities to ensure timely and high quality deliverables
Develop a monitoring plan as well as monitoring tools
Collaborate with other functional departments to identify issues and risks to clinical activities; assists in the development of mitigation plans to minimize risk

Requirements

Bachelor’s degree or RN in a life science or related field of study
Ten (10) years’ clinical research trial and/or monitoring experience
Thorough knowledge of ICH-GCP guidelines and applicable regulations
Experience working on clinical trials in the pain space (acute or chronic)
Excellent leadership skills, promoting motivation and empowerment of others

Benefits

Health insurance
401(k) matching
Paid time off
Flexible work arrangements
Professional development opportunities

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical researchstudy managementpatient recruitmentmonitoring plan developmentrisk mitigation planningclinical trial monitoringICH-GCP guidelinesregulatory compliancedata analysisstudy site management

Soft Skills

leadershipmotivationempowermentcustomer servicecollaborationproblem-solvingcommunicationstrategic planningorganizational skillsteam management

Certifications

Bachelor’s degreeRegistered Nurse (RN)