Assc Medical Director (Md) / Clinical Research Physician (Md) - Onsite, Madison Wi

Fortrea

2+ years

Not Disclosed

Madison

10 Jan. 18, 2025

Job Description

Job Type: Full Time Education: MD/DO Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Associate Medical Director (MD) / Clinical Research Physician (MD)
Location: Madison, WI (ONSITE)
Category: Clinical
Job ID: 2432655

Job Overview

Fortrea is seeking a Clinical Research Physician/Associate Medical Director to provide onsite medical coverage at our Clinical Research Unit in Madison, WI. This full-time, office-based position offers the opportunity to work with leading pharmaceutical, biotechnology, and medical device companies in Phase 1 trials. You will be directly involved in ensuring the safety and well-being of participants while witnessing the development of innovative medical treatments and technologies.

Key Responsibilities

Medical Oversight:
- Provide medical coverage and ensure the safety and welfare of participants in the clinical research unit.
- Administer test articles or delegate this to nursing staff as appropriate.
- Perform pre-study and on-study physical exams to ensure participants meet the inclusion/exclusion criteria.
- Ensure physical and mental well-being of volunteers at the conclusion of the study.
Protocol and Study Management:
- Review and evaluate study protocols and provide clinical and scientific support.
- Present protocols at IRB/IEC meetings and assist with study initiation.
- Act as Principal Investigator/Co-Investigator as assigned by the Medical Director.
- Review and sign CRFs at the conclusion of the study.
Collaboration & Compliance:
- Interact with regulatory bodies, Operations, and Client Managers.
- Inform relevant stakeholders (Principal Investigator, IRB/IEC, Sponsor) of important events.
- Assist with sponsor visits and other duties as required.

Qualifications

Education & Licenses:
- MD or DO degree.
- Active and unrestricted Wisconsin Medical License and DEA certification.
- ACLS/CPR/AED certification.
Experience:
- Minimum 2 years of clinic/patient care experience.
- Specialization in Family Medicine or Primary Care preferred.
- Previous Clinical Trials experience preferred but not required.
Skills:
- Strong interpersonal and communication skills.
- Ability to work in a fast-paced, constantly changing environment.
- Comfort with technology-based systems and electronic data collection.

Compensation & Benefits

Benefits:
- Comprehensive benefits including medical, dental, vision, life insurance, STD/LTD, 401(K), paid time off (PTO), and employee recognition awards.
Work Environment:
- A fast-paced, dynamic environment that requires quick adaptability and team collaboration.

Company Overview

Fortrea is a global leader in clinical research, revolutionizing drug and device development to improve patient outcomes worldwide.

Equal Opportunity Employer Statement

Fortrea is committed to fostering a diverse and inclusive workforce. We make employment decisions based on qualifications and business needs, ensuring equal opportunities for all.

Accommodation

For accommodation during the hiring process, please contact taaccommodationsrequest@fortrea.com.

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