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Job Overview Clinical Trial Administrator (CTA) performs study related tasks as required by the Department, including (but not limited to) communicate with Project Team and members of the project team regarding study updates, maintain documentation as required by protocols, SOPs and regulatory standards, to ensure timely production of high quality clinical data, provide system's support, track inf
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Job Overview Clinical Trial Administrator (CTA) performs study related tasks as required by the Department, including (but not limited to) communicate with Project Team and members of the project team regarding study updates, maintain documentation as required by protocols, SOPs and regulatory standards, to ensure timely production of high quality clinical data, provide system's support, track inf
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Job Overview We have a great opportunity for a Veterinary Anatomic Pathologist to join our team. Come join a global team of veterinary pathologists focused on providing high quality support to nonclinical studies spanning all phases of drug development. Due to our continuous growth, we are looking for veterinary anatomic pathologists to be based at our site in Chantilly, VA. Covance's work in deve
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Job Overview We are seeking a Senior Scientist to join our Global Clinical Microbiology team. This position is based in our Indianapolis, IN Lab. The Senior Scientist will have global responsibility for internal and external technical consultation, method selection and validation and, as appropriate, method implementation, regulatory compliance and production. The incumbent will have the opportun
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Responsible for protecting the rights, safety and welfare of participants under their care. Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations. Provide medical and scientific feasibility of all new sponsor inquires. Direct test article administration or dispensation. Review and evaluate protocols and provide clinical a
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Covance
- Burlington, NC / Raleigh, NC
Job Overview We are is seeking to fill a IT Hardware Asset Specialist in Burlington, NC. This role will support all of LabCorp Holdings. There are 17 different brands under LabCorp Holding with 61k employees in 65 countries. A multi disciplinary position, the IT Hardware Asset Specialist will assist in life cycle management of Enterprise End User computing hardware assets including inventory track
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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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Manages the washroom area by prioritizing workload and equipment to be washed Organizes and maintains clean equipment in appropriate locations Maintains well documented laboratory records according to SOP's & GLPs. Reviews other equipment service technician data and identifies potential problems Pull reports and utilize information to assist with workload projections Monitors environmental conditi
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, you'll be empowered to own your career journey with mentoring, training and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients and your career. What we're looking for Study Technicians are the most successful at Covance with A motivated, hardworking and p
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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
- 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
Posted Today
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
- Indianapolis, IN / Research Triangle Park, NC
Establish a repeatable, easily manageable process to load industry data sets into global intelligence systems Attend training sessions to learn universal tools linked to MySQL database development Familiarize yourself with business development platforms to analyze and visualize data into valuable insights for more informed decision making Engage in professional development workshops to enhance you
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Covance
- Greenfield, IN / Research Triangle Park, NC
Quickly and efficiently respond to incoming calls and faxes, identify how best to assist. Document calls in appropriate tracking systems, and handle/escalate calls per established procedures. Conduct insurance verifications to understand if patient's prescribed therapy is eligible for coverage. Possibly coordinate prior authorizations, investigate alternative insurance coverage, or other funding s
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What to Expect Data Management, Mining, and Curation Learn about safety assessment data management activities, including considerations for source data and mining and reporting data Prepare data compilations that are used for comparison purposes by scientists when evaluating study data Work closely with data management colleagues, IT, and scientist to identify and develop appropriate data visualiz
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