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The VP, Non Clinical Development will provide scientific leadership, strategic planning and actively contribute to the drug development process from late stage discovery through marketed products. Accountable for leading the non clinical development process through designing and implementing non clinical strategies for successful development of the company's lead molecule
Posted 1 day ago
The Sr. Clinical Study Manager manages global clinical studies for one or more product candidates, with one or more indications, from early development to regulatory approval (Phase 1 3) and beyond, to achieve a high quality product for the marketplace and business success for company. This involves participation in all aspects of study design, execution, analysis and rep
Posted 2 days ago
Lead projects from an analytical standpoint of view, perform and oversee analytical testing of drug substance, drug products, and related materials according to written standard operating procedures (SOPs) and test methods. ESSENTIAL DUTIES & RESPONSIBILITIES Assure that all aspects of method development, validation, troubleshooting and laboratory compliance procedures ar
Posted 2 days ago
Coordinate, and administer planning, research, and development of new and existing processes, ideologies, and programs for the continued support of the preclinical and discovery departments. Conduct and collaborate with other departments within the company as well as consults with outside contract organizations on research and development projects relevant to long term ob
Posted 3 days ago
The Trial Master File (TMF) Manager is responsible for developing and implementing processes, systems, and training programs to ensure consistent creation, maintenance, inspection readiness, and archival of BioCryst TMFs in accordance with Standard Operating Procedures (SOPs), GCP and ICH guidelines. This individual is experienced and proficient in set up, indexing, track
Posted 3 days ago
The Director of Regulatory Affairs at BioCryst Pharmaceuticals will be responsible for ensuring robust regulatory drug development strategies, accurate and timely regulatory submissions for BioCryst, as well as collaborating in general strategic drug development program implementation. This position will work closely with product development core teams and sub teams as th
Posted 3 days ago
The Clinical Scientist is responsible for ethical, medical and scientific rigor in development, conduct and reporting of assigned clinical studies across all stages of drug development and commercialization. Responsible for medical and scientific quality in the design, planning, initiation and successful completion of assigned clinical trials for new or marketed drugs for
Posted 3 days ago
The candidate for the Patent Counsel position will be responsible for a wide array of duties related to creating and managing BioCryst's patent portfolio. Candidates will have a strong background in the life sciences and passion drug development & will directly interact with BioCryst's research and development teams. As a member of our best in class legal team, this posit
Posted 4 days ago
The Rare Disease Specialist will compliantly market BioCryst products to our customers in the West TX area. #LI Remote ESSENTIAL DUTIES & RESPONSIBILITIES Have "game changing" conversations with our customers, compliantly utilizing effective selling techniques and marketing strategies to create and expand demand for any/all promoted brand(s) for which are responsible. Dev
Posted 4 days ago
As a field based Sr. MSL you will be a true scientific, medical expert and an extension of BioCryst Medical Affairs. You will build and facilitate strategic peer to peer relationships with key Health Care Providers (HCP) in the assigned region. You will be providing credible and unbiased scientific information, identifying and executing the strategic Medical Affairs Plan
Posted 4 days ago
The Corporate and Securities Paralegal will provide support to the Securities and Corporate Governance team in the company's Legal department on the company's global entity management, SEC filings, corporate transactions, and corporate governance matters. This position is based in Durham, NC and reports to the Exec. Director, Securities, Corporate Governance & Assistant C
Posted 4 days ago
The Rare Disease Specialist will compliantly market BioCryst products to our customers in the Richmond, VA area. #LI Remote ESSENTIAL DUTIES & RESPONSIBILITIES Have "game changing" conversations with our customers, compliantly utilizing effective selling techniques and marketing strategies to create and expand demand for any/all promoted brand(s) for which are responsible
Posted 6 days ago
The Rare Disease Specialist will compliantly market BioCryst products to our customers in the Louisiana or Arkansas area. #LI Remote ESSENTIAL DUTIES & RESPONSIBILITIES Have "game changing" conversations with our customers, compliantly utilizing effective selling techniques and marketing strategies to create and expand demand for any/all promoted brand(s) for which are re
Posted 7 days ago
Accountable for assisting with the toxicology strategy for successful development of the company's small molecule and biologics across all stages of development. Responsibilities include the design, planning, initiation and successful completion of toxicology studies required for new or marketed drugs for all phases of development. #LI Remote ESSENTIAL DUTIES & RESPONSIBI
Posted 10 days ago
Accountable for quality of medical and scientific conduct of assigned Phase I IV clinical studies and/or drug product development. May lead product development medical teams if more than 1 physician supports a program. In addition, the Sr. Medical Director may be consulted or have responsibilities for Phase IV studies conducted by medical affairs if appropriate. The Sr. M
Posted 10 days ago
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