Provides after-hours medical coverage for clinical studies.
Adheres to all enterprise policies, work instructions, standard operating procedures, and project plans.
May support responses to Requests for Proposals (RFPs) or Bid Defense Meetings (BDMs), upon request.
May represent the Company at scientific meetings, upon request.

Requirements

Must be located in the United States with no sponsorship needs to be considered for this role.
Provides medical oversight of assigned clinical studies in the duty as a medical monitor.
Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department.
Responsible for protocol design and development, upon request.
Develops and delivers project-specific and therapeutic training to project team members and clinical site staff; provides training to customer staff as needed.
Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts.
Provides medical input into data collection tools, monitoring plans, and review and analysis plans.
Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data.
Maintains in-depth knowledge of FDA and worldwide drug development regulations and national and ICH Good Clinical Practice (GCP) guidelines.

Benefits

Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time

Applicant Tracking System Keywords

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

Hard Skills & Tools

medical oversightprotocol designdata collection toolsmonitoring plansreview and analysis plansproject-specific trainingtherapeutic trainingclinical data reviewdrug safetypharmacovigilance

Soft Skills

communicationleadershiporganizational skillsinterpersonal skills