Medical Director

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.

Job Title: Medical Director

Location: US Remote

Function: Strategy and Safety

Education: MD with specialty in Gynecologic Oncology, ex. Endometrial Cancer

DESCRIPTION:

The Medical Director will offer strategic input on current and prospective clinical projects, support site investigators, and oversee medical monitoring in relevant clinical trials. The ideal candidate will have extensive experience in clinical trials focused on gynecologic oncology across all phases, with a proven track record of successfully leading and conducting trials at either sites or sponsors. A strong background in developing and executing clinical trials with innovative treatments, particularly immunotherapy or small molecule therapy, is preferred.

Key Responsibilities:

• Provide strategic input on potential projects, supporting proposal writing and bid-defense meetings with a deep understanding of the current clinical research landscape in gynecologic oncology.
• Collaborate closely with Clinical Operations to ensure trials are effectively operationalized to meet milestones.
• Review and address site and CRA queries regarding inclusion/exclusion criteria.
• Prepare listings of protocol deviations and adverse events for regular meetings, perform initial reviews for coding, and reconcile coding based on inputs from clinical and medical teams.
• Support medical writing for protocols and study reports.
• Prepare and review protocol deviation listings and code deviations per protocol deviation guidance.
• Draft appropriate study plans and adverse event listings.
• Assist in the medical monitoring and management of clinical trials.

EDUCATION AND EXPERIENCE REQUIRED:

• Licensed MD
• 5+ years of experience working in clinical trials as a Medical Director with medical monitoring, trial design / strategy in Gynecologic Oncology and or equivalent relevant experience
• Gynecologic Oncology specifically Endometrial Cancer

PREFERRED SKILLS:

• Strong communication
• Medical Writing
• Independent worker
• Excel
• CTMS

COMPENSATION & BENEFITS:

Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits.

EMPLOYMENT TYPE:

Contract; Part time, Hourly

COMMITMENTS:

• Hourly as project requires
• Willing to work in shifts as and when needed.

DISCLAIMER:

Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.