Job Description

Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing cancer research in the clinical trial setting. Our passionate team is committed to bringing cancer treatments of the future to the world of today. We are seeking an experienced physician leader to head our Medical Monitoring Unit, ensuring the medical and scientific integrity of oncology clinical trials across Phase I–III studies. This is a role that goes beyond individual study oversight, requiring the ability to manage people, complexity, and competing priorities within a dynamic and growing portfolio. The ideal candidate brings deep oncology and medical monitoring expertise, combined with strong managerial capability, sound judgment, and the ability to navigate fast-moving, data-rich, and often ambiguous environments. They will balance scientific rigor with operational practicality, communicate effectively across stakeholders, and lead with a high level of ownership, credibility, and strategic perspective. Reporting directly to the Vice President, Medical Affairs, this position offers a remote or hybrid work model, depending on the candidate’s location and preference. Key Responsibilities Lead, manage, and further develop the Medical Monitoring Unit, including direct oversight of multiple Medical Monitors Ensure consistent, high-quality medical monitoring across oncology trials from Phase I through Phase III Provide expert medical guidance on protocol interpretation, safety events, eligibility, and benefit-risk assessment Act as a senior medical point of contact for sponsors, investigators, and internal stakeholders Drive consistency, quality standards, and best practices across studies and across the team Manage resource allocation and priorities across a complex and evolving study portfolio Contribute to study and portfolio-level planning, including alignment with budgets and cross‑functional collaboration Support hiring, coaching, and retention of high-performing medical staff Partner closely with cross‑functional teams including Clinical Operations, Drug Safety, Medical Writing, and Regulatory Qualifications Medical Doctor (MD) required; oncology specialization strongly preferred 8–10+ years of experience in clinical research Proven experience as a Medical Monitor in oncology clinical trials (Phase I–III) Strong background in safety review and medical decision‑making in active oncology studies Demonstrated experience in people management and team leadership Experience managing multiple studies or programs simultaneously Strong understanding of clinical trial design and regulatory frameworks (ICH‑GCP, FDA, EMA) Fluent English required; Spanish is a plus CRO experience strongly preferred; Pharma experience will also be considered What TRIO Can Offer You Opportunity to lead a critical function within an oncology-focused organization High‑impact role with visibility across senior leadership Exposure to a diverse and scientifically meaningful oncology portfolio A role combining medical depth, leadership responsibility, and strategic influence Annual compensation review with opportunities for professional growth 3 weeks of vacation plus paid December Holiday Closure 10 days paid personal/sick time 1 paid volunteer day per year A top tier, comprehensive Health / Medical plan for you and your family – monthly premiums paid for by TRIO Up to 5% matching 401(k) program Flexible working hours to promote work‑life balance Monthly Internet Allowance to support working from home Remote work arrangements anywhere across the USA and one‑time home office allowance Out‑of‑country work: employees can request to work internationally for a short period of time each year Employee Family Assistance Program to support you and your family during difficult times Employee Recognition Program to reward long‑term employees Employee Referral Bonus Program Pay Range : $150,000 to $200,000 USD – salary to be influenced by education, experience, location, knowledge, skills, abilities, internal equity, and market data. #J-18808-Ljbffr

Job Tags

Similar Jobs