Medical Monitor, Oncology

Join Our Team as a Medical Monitor

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

About this role

The Medical Monitor is responsible for ensuring the highest standards for patient safety, trial conduct and data integrity.

As part of our SRS team you will be dedicated to one sponsor, a global biotech company known for innovative therapeutics for the treatment of cancer.

Key Responsibilities:

• Engage, develop and maintain strong working relationships with Clinical Investigators.
• Active participation in clinical data review, analysis and presentation (including writing and/or review of clinical study reports, patient narratives, patient profiles).
• Protocol execution, including interactions with clinical operational teams and study sites (study coordinators and Investigators).
• Provide support for trial initiation and conduct (e.g., IRB responses, CRF and database reviews).
• Interact with and support company regulatory function to ensure timely contribution of patient information for any regulatory requests or medical related questions.
• Partner with pharmacovigilance to ensure timely and accurate safety reporting to regulatory authorities.
• Close interaction with appropriate functions to ensure full understanding and clarity and ability to educate and update sites around the scientific basis for targeted therapies under development.

Qualifications:

• MD
• Formal training in Medical Oncology and/or Hematology and/or extensive oncology clinical development experience is preferred (e.g., patient cancer care experience, residency and fellowship training included)).
• Experience or exposure to clinical development in leukemia and lymphoma is preferred.
• Minimum of 5 years in Biopharma / Pharma industry as a medical monitor or study director
• Ability to work independently, with direction and within project teams.
• Strong verbal and written communication skills; comfortable with public speaking.
• Strong organizational skills, including the ability to prioritize workload.
• Strong interpersonal skills; able to engage and collaborate with a variety of internal and external personnel.
• Ability and willingness to travel up to 20 % of the time (international and domestic).

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our cores values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unifed force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference

Department SRS North America Locations USA Remote status Fully Remote Employment type Full-time REQ ID w Work Arragement Remote