This retained search is being conducted on behalf of our rapidly-growing client focused on early cancer detection. The Vice President, Medical Affairs will be a key member of the management team. One will develop and implement strategies in medical affairs that affirm our client’s credibility in the medical community and position the company as a leading-edge organization.
This retained search is being conducted on behalf of a global pharmaceutical and diagnostics company that has FDA approved innovative oncology diagnostics. Their highest priority is to improve diagnostic and therapeutic approaches to human health by enabling detection and analysis of important cells and to provide researches and oncologist the access to unparalleled precision in molecular characterization.
We have been retained by our client to hire a Clinical Development Director. Our client has identified a gap and expertise and needs a clinician to help develop high level strategic clinical development plans for products from conception through reimbursement and post market needs. They have successful achieved a marketed product and have a full pipeline. The goal is to develop strategies on clinical evidence development. This is not about executing a protocol but about setting the strategy and being able to know what goes into the protocol, know how it is structured to assure that patient enrollment will work and that they can access the patients in a reasonable time-frame during the care of their journey.
This Market Access Director search is being conducted on behalf of a global pharmaceutical and diagnostics company that has FDA approved innovative oncology diagnostics.
Although the role is remote based, one will be responsible for ensuring market adoption of the products and/or services with national, regional, and governmental payers. This includes developing a well-defined market access strategy. This will include the development of…
This Medical Director search is being conducted on behalf of our global biopharmaceutical company. This individual is accountable for the ethical and scientific integrity of the plans and studies and responsible for the preparation of medical components of Investigator Brochures, ethics, IND and other regulatory communications.
One must have the ability to draw on previous clinical research experience to design clinical development plans, to plan and lead studies, to anticipate potential problems and to take appropriate action.
This Clinical Development search is being conducted on behalf of our global biopharmaceutical client. We seek an individual with proven leadership skills and the ability to interact collaboratively in a cross functional environment. One must be able to integrate and analyze non-clinical and clinical data as well as data/input from multiple internal and external functional areas. This is an individual contributor role, one must be able to work independently with minimal supervision.