Medical Director (Oncology)
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve.
Title: Medical Director (Contract, Remote | Oncology – Multiple Myeloma)
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
Description:
We are seeking an experienced Medical Director to lead clinical trial strategy, design, and execution for oncology studies, with a focus on multiple myeloma. This individual will serve as the primary medical lead and Medical Monitor, ensuring patient safety while partnering cross-functionally to drive high-quality clinical development programs.
This is a high-impact, fully remote contract opportunity ideal for a physician-scientist with strong industry experience and a passion for advancing cancer therapies.
Key Responsibilities
Qualifications
Position Details
Why This Role
This is an opportunity to play a key leadership role in advancing innovative oncology therapies, working alongside a collaborative and mission-driven team dedicated to improving patient outcomes.
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Title: Medical Director (Contract, Remote | Oncology – Multiple Myeloma)
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
- Duration: 6 months (potential for conversion)
- Pay rate: Up to $190/hr (flexible based on experience)
- Job Location: Remote, US (East Coast working hours)
- Job#: bh18910
Description:
We are seeking an experienced Medical Director to lead clinical trial strategy, design, and execution for oncology studies, with a focus on multiple myeloma. This individual will serve as the primary medical lead and Medical Monitor, ensuring patient safety while partnering cross-functionally to drive high-quality clinical development programs.
This is a high-impact, fully remote contract opportunity ideal for a physician-scientist with strong industry experience and a passion for advancing cancer therapies.
Key Responsibilities
- Lead the design and development of clinical study protocols, Investigator’s Brochures, and Clinical Development Plans
- Serve as Medical Monitor, overseeing patient safety and reviewing clinical data for assigned trials
- Collaborate with cross-functional teams (Clinical Operations, Regulatory, Data Management, etc.) to ensure efficient study execution
- Contribute to regulatory submissions including INDs, CTAs, safety reports, and responses to health authorities and IRBs/Ethics Committees
- Provide clinical and scientific input into key study documents (ICFs, CRFs, SAPs, CPAPs, CSRs)
- Support lifecycle management and data generation strategies to address unmet medical needs
- Partner with Medical Affairs teams to support scientific communications, publications, and external engagement
- Build and maintain relationships with key opinion leaders (KOLs), investigators, and external stakeholders
- Stay current on scientific and clinical advancements through literature review and conference participation
- Author manuscripts and contribute to publication plans
- Present data at scientific and medical meetings as needed
- Participate in business development and due diligence activities as appropriate
Qualifications
- MD, DO, or PhD required (MD/DO strongly preferred)
- 5+ years of clinical trial experience in academic or industry settings
- Minimum 3 years as an attending physician in oncology, hematology, internal medicine, or related specialty
- Oncology experience required; multiple myeloma experience strongly preferred
- Prior pharmaceutical/biotech industry experience, including clinical development and/or trial leadership
- Strong understanding of GCP, clinical study design, regulatory requirements, biostatistics, and pharmacokinetics
- Experience contributing to regulatory submissions and scientific publications
- Excellent communication and collaboration skills
- Ability to thrive in a fast-paced, matrixed environment
Position Details
- Start Date: ASAP
- Duration: 6 months (with potential for extension)
- Compensation: Up to $190/hour (flexible based on experience)
- Location: 100% Remote
- Therapeutic Area: Oncology – Multiple Myeloma
Why This Role
This is an opportunity to play a key leadership role in advancing innovative oncology therapies, working alongside a collaborative and mission-driven team dedicated to improving patient outcomes.
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Meet Your Recruiter
