Instagram
youtube
Facebook

Medical Director (Oncology Contract)

5+ years
Not Disclosed
10 Feb. 18, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Medical Director (Oncology Contract)
Location: Remote (US)
Function: Strategy and Safety
Education Required: MD with specialty in Gynecologic Oncology (e.g., Endometrial Cancer)


Company Overview:

Sitero is an emerging leader in clinical services and software solutions within the life sciences industry. With expertise in a variety of therapeutic areas, we focus on delivering innovative, technology-enabled solutions that allow clients to focus on their core strengths. Our team offers high-touch services and technology for clinical trials, from early-phase studies through Phase III, with an emphasis on ethics, compliance, and safety.


Job Description:

The Medical Director will provide strategic guidance on current and prospective clinical projects, support site investigators, and oversee medical monitoring for relevant clinical trials. This role requires extensive experience in gynecologic oncology clinical trials across all phases, especially in trials involving innovative treatments such as immunotherapy or small molecule therapy.


Key Responsibilities:

  • Strategic Input & Support:

    • Provide strategic input on potential projects, including supporting proposal writing and bid-defense meetings.

    • Offer expertise on the current clinical research landscape in gynecologic oncology.

  • Collaboration with Clinical Operations:

    • Work closely with Clinical Operations to ensure trials are operationalized effectively and meet milestones.

  • Trial Management:

    • Review and address site and CRA queries regarding inclusion/exclusion criteria.

    • Prepare and review protocol deviation listings, adverse event reports, and reconcile coding inputs.

  • Medical Monitoring & Reporting:

    • Assist in the medical monitoring and management of clinical trials.

    • Support medical writing for protocols and study reports, including drafting study plans and adverse event listings.


Education & Experience Required:

  • Education: Licensed MD

  • Experience:

    • 5+ years of experience in clinical trials as a Medical Director.

    • Experience in medical monitoring, trial design, and strategy in Gynecologic Oncology (specifically Endometrial Cancer).


Preferred Skills:

  • Strong communication skills.

  • Proficiency in medical writing.

  • Ability to work independently.

  • Experience with Excel and CTMS.


Compensation & Benefits:

  • Competitive salary.

  • Variable pay.

  • Paid time off.

  • Healthcare and retirement benefits.


Employment Type:

Contract (Part-Time, Hourly)


Commitments:

  • Hourly commitment based on project requirements.

  • Willingness to work in shifts as necessary.