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Covance
- San Francisco, CA
Job Overview Covance is seeking candidates for a Site Selection Lead II. The Site Selection Lead II can be home based or remotely located anywhere within the United States. Develop, in conjunction with the Global Feasibility Lead, the initial site list for feasibility and site identification Full oversight of the Feasibility/Site identification process survey development and programming, local res
Posted Today
Covance
- San Francisco, CA
Job Overview Lead Project Data Manager (CDM I) permanent, salaried Remote from anywhere in the U.S. or Canada Get ahead in your career and make a difference in people's lives! Are you a self starter who knows how to take initiative in your daily work? Would you enjoy making a real difference in the lives of others. If you are looking for a high energy position in a collaborative environment, learn
Posted Today
Job Overview Our mission is to help our clients bring the miracles of medicine to market sooner join us for your next career move. Reporting to the Executive Medical Director, the primary role of the Medical Director / Physician is to provide subject matter expertise in support of advancing clinical trials and drug development supporting our haematology group. In partnership with Covance clients,
Posted Today
Job Overview CRA I or II, Oncology Experience Required Why settle for one thing when you can have everything. Covance gives you the best two for one opportunity for career growth. Who doesn't want twice the perks working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. As a Covance employee dedicated to an FSP project you will bring your sp
Posted 1 day ago
Job Overview Covance is seeking candidates for a Clinical Applications Programmer II. This role will be home based or remotely located within the United States. Expected to assist with leading EDC Builds and mentor the study team in setting up Medidata RAVE, Oracle Inform, or SAS or any other proprietary software. Oversees the project work of technical and design staff. Manage projects within the
Posted 2 days ago
Job Overview Reporting to the Executive Medical Director, the primary role of the Medical Director is to provide subject matter expertise in support of advancing clinical trials and drug development supporting our haematology group. In partnership with Covance clients, he/she will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Medic
Posted 2 days ago
Job Overview The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations ONCOLOGY CTL group. The Clinical Team Lead (CTL) is responsible and accountable for the execution of the clinical operations component of the project, at the global or regional level, as assigned. The CTL is responsible for working cross functionally, within a matrix environment, to ensure succ
Posted 6 days ago
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or ot
Posted 7 days ago
Job Overview Senior Clinical Scientist Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada Why settle for one thing when you can have everything ? Covance gives you the best two for one opportunity for career growth. Who doesn't want twice the perks ? W orking at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeut
Posted 7 days ago
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to provide subject matter and drug development expertise in support of Respiratory/Pulmonary, Critical Care, and Infectious Disease drug development trials. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Medical Director o
Posted 7 days ago
Job Overview CRA Drug Accountability (Unblinded CRA) Covance is seeking an Unblinded CRA to cover the Western Region of the US. This is a specialized CRA role which primarily focuses on drug accountability at a site level across a range of protocols and therapeutic areas. Essential Job Duties Responsible for all aspects of study site monitoring including routine monitoring and close out of clinica
Posted 7 days ago
to include; Client Relationship & Business Development Activities Partnering with GCO to develop new and enhance existing client relationships where possible Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team Leverage known and builds new relationships with investigators/sites to performs site/ investigator feasibility and to support op
Posted 9 days ago
Develop, direct and review the delivery of world class veterinary and animal welfare services that contribute to the successful implementation of early development strategy and generate high customer satisfaction. Lead a high performing team of animal welfare experts and laboratory animal veterinarians in the USA by focusing on agreed objectives delivery, developing leadership capacity and promoti
Posted 14 days ago
Covance
- San Carlos, CA
Job Overview We are presently seeking an Attending Veterinarian to join our team in San Carlos, CA. The incumbent will be primarily responsible for providing veterinary health care for laboratory animals, giving advice regarding the care and maintenance of laboratory animals, and providing training for technicians. Additionally, he/she will monitor animal health and welfare in compliance with appl
Posted 14 days ago
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or ot
Posted 22 days ago
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