My client, a commercial-stage, publicly traded, medical device company developing products to help patients with venous diseases, is hiring an experienced Regional Clinical Research Associate (CRA) homebased in California to conduct site monitoring visits and site management activities on Cardiovascular Medical Device studies utilizing good clinical practice (GCP) and all applicable regulations. This is a California
We are seeking a highly motivated, PhD-level Immunologist with cellular and molecular biology experience for the role of Research Scientist I. The position will be based in North Brunswick, New Jersey, and will directly report to Chief Scientific Officer. This individual will be required to engineer new biological entities to screen, clone, and develop with multiple partners. Practical, ‘out-of-the-box’ thinking is
Startup biotechnology company in San Francisco seeks a Scientist - Myogenesis to join a scientific team developing a proprietary technology platform to targeting various regenerative pathways critical for the establishment of complex diseases. This well funded start-up offers an exciting environment where your input matters. Requirements for Scientist - Myogenesis: * PhD in molecular biology, biotechnology, ph
Startup biotechnology company in San Francisco seeks a Research Associate, to join a scientific team developing a proprietary technology platform to targeting various regenerative pathways critical for the establishment of complex diseases. This well funded start-up offers an exciting environment where your input matters. Requirements for the Research Associate - Cell Engineering: * Bachelor's degree in biotechnol
be a part of a team that is passionate and dedicated to saving lives threatened by the global public health crisis of bacterial infections, We strive to offer a dynamic work environment in which innovation, teamwork, knowledge and flexibility are valued. Our novel antibiotics portfolio has the unique ability to provide providers and patients with a range of solutions that can meet the tremendous need for treating ser
Remote Medical Writer for Pharmaceutical company. Must have Clinical writing and Submission experience This position works to write scientifically valid, complete, and consistent documents, including but not limited to clinical study protocols, IND, IND amendments, regulatory responses clinical study reports (CSRs), investigator's brochures (IBs), briefing books, and other similar items. Key Responsibilities * Und
The Sr. CTM is responsible for the execution of clinical trials and will review, monitor, and ensure adherence to protocols. The Sr. CTM will: * Participate in the design & execution of clinical trials, development of critical clinical documents & oversee operational implementation * Independently manage and communicate to management overall clinical operations plan for clinical trials including internal and exter
My client, a commercial-stage, publicly traded, medical device company developing products to help patients with venous diseases, is hiring an experienced Regional Clinical Research Associate (CRA) homebased in the greater NYC area to conduct site monitoring visits and site management activities on Cardiovascular Medical Device studies utilizing good clinical practice (GCP) and all applicable regulations. This is a
My client, a commercial-stage, publicly traded, medical device company developing products to help patients with venous diseases, is hiring an experienced Regional Clinical Research Associate (CRA) homebased in Michigan to conduct site monitoring visits and site management activities on Cardiovascular Medical Device studies utilizing good clinical practice (GCP) and all applicable regulations. This is a Michigan hom
My client, a commercial-stage, publicly traded, medical device company developing products to help patients with venous diseases, is hiring an experienced Regional Clinical Research Associate (CRA) homebased in Texas to conduct site monitoring visits and site management activities on Cardiovascular Medical Device studies utilizing good clinical practice (GCP) and all applicable regulations. This is a Texas home-offi
