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Participate in the full stack design and development of web and mobile based SaaS solutions for integrating, processing and visualizing data at scale. Participate in the full development cycle from product inception, research and prototyping to release in production. Work with a team of software engineers to write production quality code while implementing your own ideas. Provide support for the r
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Covance
- San Francisco, CA / Philadelphia, PA / Pittsburgh, PA / 19 more...
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
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Covance
- Princeton, NJ / Nashville, TN / Raleigh, NC
Developing understanding of ICH/GCP, core Clinical Research documentation, soft skills/business communication, clinical trial management, and business client interactions General On Site Monitoring Responsibilities Observe Senior CRAs, CRA 2 and CRA 1 with on site tasks as required and according to training goals (e.g. review of Case Report Forms and Study File Notebook, drug accountability) Engag
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Covance
- Princeton, NJ / Chicago, IL / New York, NY / 4 more...
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical Director will play a key role in people leadership/management, client relations, a
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Covance
- Princeton, NJ / Seattle, WA / Phoenix, AZ / 3 more...
Job Overview Reporting to the Executive Medical Director, the primary role of the incumbent will be to serve as a physician providing subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Sr. Medical Director will play a key role in people leadership/management, client relations, a
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Covance
- Princeton, NJ / Durham, NC / Dallas, TX / 2 more...
Job Overview Discover new opportunities to grow your career as a Medical Director! 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. In partnership with Covance clients, he/she will be expected to be a key contributor to the medical strategy and execu
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Job Overview Exciting Opportunity to join Covance as a Post Life Necropsy Technician in Somerset, NJ ! Company Overview If you've ever taken a medicine, received a vaccine or had blood drawn for a lab test, you've already benefited from the powerful work of 57,000+ exceptional employees across Covance and LabCorp. By supporting leading pharmaceuticals and 600+ biotech companies through our contra
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Job Overview Exciting Opportunity to join Covance as a Study Technician in Somerset, NJ ! Company Overview If you've ever taken a medicine, received a vaccine or had blood drawn for a lab test, you've already benefited from the powerful work of 57,000+ exceptional employees across Covance and LabCorp. By supporting leading pharmaceuticals and 600+ biotech companies through our contract research or
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Conduct of animal studies including dosing of both large and small animal species (mice, rats, rabbits, dogs and non human primates via various routes including but not limited to iv, po, dermal, subq and inhalation) and sample collections (blood, urine, etc.). Maintain clear and timely observations and health monitoring on all study animals. Record accurately and timely study related data in comp
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Job Overview Are you passionate about market intelligence, while making a difference in patients' lives? Do you want to leverage your expertise in market research, modeling and insights to drive positive change, alongside executive leadership? If you answered yes to these, we'd like you to consider joining Covance as an Associate Director, Market Intelligence. In this role, you will Leadership Man
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Covance
- Princeton, NJ / Raleigh, NC / Burlington, NC
Collect and manage current and historical exposure information and prepare annual underwriting submissions for casualty program Conduct contract reviews when there is a discrepancy from standard language Check accuracy of insurance policies, prepare insurance coverage summaries Analyze loss experience at the location, business unit, and corporate level to identify trends Manage Certificate of Insu
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Covance
- Princeton, NJ / Seattle, WA / Austin, TX / 27 more...
Job Overview Senior Project Manager, Oncology Home Based Anywhere in the US or Canada Therapeutic Area Experience Required Oncology At times working under the direction of a Project Director; the Senior Project Manager oversees and manages domestic, regional and/or international projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedul
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Covance
- Princeton, NJ / Miami, FL / Chicago, IL / 4 more...
Job Overview Reporting to the Vice President and Global Therapeutic Area Head , the incumbent will function as a leader supporting clinical trials by serving as global lead project physician and as a program level physician across multiple indications for a given compound. Furthermore, he/she will provide subject matter and drug development expertise to be a key contributor to the medical strategy
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Job Overview Covance is currently seeking candidates for an Associate II Regulatory Submissions position. The Associate II Regulatory Submissions position will be office based in Princeton, NJ. Responsible for providing support to regulatory managers and others for the timely submission of information to Regulatory Authorities in support of investigational and marketed products. Interacts with Reg
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Covance
- Philadelphia, PA / Pittsburgh, PA / Princeton, NJ / 7 more...
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 Today
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