This is for an opportunity at a privately held, clinical-stage biopharmaceutical company developing a potentially best-in-class MDM2 inhibitor. Launched in 2018 by proven industry veterans, we have brought together scientists and clinicians with a deep understanding of hematology and oncology and an experienced leadership team. Together, we’re building an exciting biotechnology company with a culture defined by caring, ambition, dedication and teamwork! Job Summary **Responsibilities**: - Responsible for implementing enrollment site strategies in clinical trials
- Attend SIVs to train investigators and site personnel of the protocols including scientific rationale and eligibility criteria
- Train investigators and site staff on administration of the investigational product
- Provide initial and continuous training, education and support for clinical center personnel on clinical trial protocols, clinical process, and data questions
- Accelerate enrollment of patients through investigator engagement activities, referrals and implementing awareness initiatives
- Engage KOLs and continue to garner interest in the investigational product and clinical development plan




- Support the clinical trial objectives; responds to or triages questions for appropriate escalation
- Contribute to the organization, preparation, and execution of investigator and study meetings in collaboration with the study team and external collaborators
- Collaborate on the preparation of scientific material for presentations
- Provide enrollment support along with fellow medical affairs, clinical scientists and medical officers Qualifications: - Advanced Clinical/ Science Degree is preferred (e.g., PharmD, PhD, MSN, NP, RN)
- 3+ year experience in the biopharmaceutical industry preferably in clinical field support
- Clinical knowledge in hematology and patient management issues preferred
- Working knowledge of Good Clinical Practices, ICH, and other regulatory requirements for clinical studies
- Excellent communication (written and orally) of clinical and scientific data to a variety of audiences
- High level of organizational and project management skills
- Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy
- Ability to travel up to 70% of time

📌 Medical Science Liaison- Europe (Roma)
🏢 TriNet Pharma
📍 Roma