Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s)
Serving as the lead clinical scientist on the clinical trial team
Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director
Collaborating cross-functionally in the development of Protocol and related study materials
Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming
Providing 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 years of pharmaceutical, clinical drug development, project management and/or medical field experience OR PhD / PharmD
Demonstrated ability to drive and manage scientific activities on clinical protocols
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)
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
Must be proficient in English

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 protocol executionmedical monitoringdata interpretationCRF designdata collectionproject managementclinical trial data analysisscientific mentorshipclinical researchpharmaceutical development

Soft Skills

analytical skillsplanningtime managementprioritizationcollaborationleadershipmentorship

Certifications

Bachelor's degreeMaster's degreePhDPharmD