The Med Dir is responsible for external-facing interactions with medical experts and other stakeholders, and is expected to build and maintain strong opinion leader relationships. The GMAL engages in external collaborations in order to gain insight and to facilitate clinical development and life cycle plans.
This Director of Medical Monitoring will involve acting as Medical Monitor for numerous Oncology trials.The Director will be assigned as a leader of a group of Medical Monitors within Oncology and/or geographical region.
Responsible to implement behavioral Health medical policy, technology assessment and clinical practice standards developed by Magellan corporate and participates in management of the inter-rater reliability process to ensure consistency between reviewers. Provides input regarding the need for modifications and additions to medical policy. May participate on corporate medical policy and clinical guideline committees.
You will need to be comfortable in conducting peer to peer discussions with medical professionals and medical and scientific colleagues. You also need a strong clinical science background in order to understand how to design clinical studies for evidence generation and evaluate data.
Responsible for the supervision of all clinical provider personnel within the clinic which will include supervising and evaluating Nurse Practitioners and Physician Assistants working in collaborative practice, including chart review.
The medical records director plans, develops, and administers medical record systems for nursing centers in accordance with state and federal regulations as well as professional standards of practice and company and facility policies and procedures.
In this role, the selected candidate will be responsible for the development, management and approval of scientific methods for design of clinical protocols, case report forms, guidelines and study reports.