Category Archives: biotech-pharma-openings
Description of Role We are currently seeking an experienced, creative, and highly motivated Process Developer to build in-house manufacturing capabilities including but not limited to: innovative systems, building a team, and identifying and removing barriers to efficient production of complex …..
The Associate Director, Pharmacovigilance & Epidemiology, under the guidance of the Director of Medical Safety Science, Risk Management, is responsible for liaising with PVE Operations, managing clinical trial support activities, and accessing data for Aggregate Reports. The candidate should be …..
Job Description The Senior Manager, Pharmacovigilance & Epidemiology is responsible for or supports various pharmacovigilance and risk management/minimization activities for investigational and marketed products Responsibilities (include but are not limited to): Author and coordinate/project manage development of periodic safety reports …..
The Medical Director will join the global heart failure clinical development program, which includes approved and multiple investigational therapies across all phases of development. Responsibilities Provide clinical and scientific leadership and oversight for generation of scientific evidence, especially the development and execution …..
The Early Development Leader (EDL) will be responsible for providing scientific/ medical direction and leadership for pre-clinical/ early clinical programs for biotech’s Early Development cardiovascular-metabolic pipeline. The Medical Director will lead the early phase clinical development of compounds in the cardiovascular-metabolic …..
Tanner & Associates is recruiting a Clinical Research Medical Director in Bone Health for a large biotech company based in California. Please send CV to email@example.com Key Responsibilities: Supporting the development, execution and communication of the global scientific/medical evidence plan …..