Lead the scientific planning and execution of one or more clinical trials or significant aspects thereof
Serve as the lead clinical scientist on the clinical trial team
Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director
Collaborate cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments)
Provide tactical/scientific mentorship to other clinical scientists

Requirements

Bachelor's degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR master's degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD degree
Degree in life sciences, preferred
Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Experience in conducting global clinical trials, including trial initiation through database lock

Benefits

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays, vacation, and compassionate and sick days

Applicant Tracking System Keywords

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

Hard Skills & Tools

clinical trial managementdata interpretationprotocol developmentclinical data reviewmedical monitoringproject managementanalytical skillsclinical researchregulatory complianceglobal clinical trials

Soft Skills

leadershipcollaborationmentorshipcommunicationtactical planning

Certifications

GCPICH