Medical Science Liaison- Europe

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

The Medical Science Liaison will work closely with investigators, clinical research associates and other study team personnel conducting the trials to ensure that the sites possess an understanding of eligibility criteria and other aspects of the protocols. This includes engaging investigators about the scientific background, study rationale, data collection and data related questions. The Clinical Trial Liaison may be involved in the identification and evaluation of trial sites and provide insight on best practices for the identification and recruitment of trial subjects. The clinical trial liaison will also engage in peer-to-peer discussions with investigators about trial data and results.

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