Senior Medical Director – Oncology

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $254.9k - $382.3k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 11%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Serve as a senior medical and scientific leader in sponsor interactions • Represent the organization as physician and subject matter expert during client meetings, scientific presentations, conferences, proposal discussions, and bid defense activities • Provide medical and scientific expertise during client feasibility assessments, including study design, patient populations, enrollment strategies, and site selection • Serve as Medical Monitor for assigned studies and provide medical oversight of patient safety, scientific rigor, and operational excellence • Review and interpret laboratory data, adverse events, medical coding dictionaries, and study data outputs • Review and provide expert input into medical monitoring plans, study protocols, statistical analysis plans, case report forms, training materials, investigator brochures, clinical study reports, and other study documents • Conduct independent medical analyses of emerging study data and communicate findings, risks, and recommendations • Collaborate with Safety/Pharmacovigilance teams on safety documentation, safety signal evaluation, and risk management • Contribute medical expertise to safety review meetings, data monitoring activities, and governance committees • Lead complex global clinical programs and guide regional medical leaders and project teams • Participate in investigator meetings and scientific advisory discussions • Mentor, coach, and develop Medical Directors, Associate Medical Directors, and other colleagues • Identify opportunities to improve processes, efficiencies, quality, client experience, scientific excellence, operational effectiveness, and innovation

🎯 Requirements

• MD, DO, MBBS or equivalent education with completion of residency in a medical or pediatric sub-specialty, including completion of a fellowship in hematology and/or oncology • At least 10 years combined experience in academic and/or industry clinical research in drug development • Experience as a Medical Monitor on clinical oncology and/or rare clinical trials is required • Clinical practice experience of a minimum of 3-5 years preferred • Board certification in hematology and/or oncology preferred • Effective written and verbal communication skills • Salesmanship and presentation skills • Proficiency and sensitivity to work in a global company with reports from varied cultures and backgrounds • Candidates must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Discretionary annual bonus • Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation