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Job Overview Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team focused environment as you explore unique career opportunities? If you are looking for a company where you can gain exposure to a wide variety of science and explore a multitude of career paths across the drug development spectrum, consider working at Covance as a Medica
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Job Overview At Covance , Improving lives and improving health is more than just a catchphrase. It's the mission that drives our 60,000+ enterprise team members across the globe. These exceptional people help solve drug development challenges and transform ideas into reality for patients. Become part of this exceptional team as an Animal Care Technician working in our Animal Research area. Day ti
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Covance
- Seattle, WA / San Francisco, CA / Portland, OR / 7 more...
Job Overview Senior Clinical Research Associate Cardiology & Oncology 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 wil
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Job Overview Responsible for the entry and accuracy of the appropriate tracking system. Communicates client disposition authorization with appropriate staff. Accurate protocol and relevant documentation interpretation (i.e., Sample Analysis Outline, client paperwork, contracts). Contacts clients routinely to determine disposition With assistance, works with Finance and/or Client Services to ensure
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Job Overview Covance's work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life saving work. Help improve patients' lives while growing your career. Covance is currently looking for a Data Reviewer Laboratory Operations to join our growing Necropsy team in Somerset, NJ . Covance's work in developing new pharmaceutical solutions
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Learns to and reviews and adjust the reporting schedule to ensure client expectations are met. Learns to and schedules and leads the prewriting meeting, as required Learns to and schedules and coordinates study report finalization efforts Learns to coordinate expedited reporting, as necessary, among global counterparts #LI NW1 Education/Qualifications Preferred Degree and/or experience in science,
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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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What to Expect Establish an understanding of basic lab practices and SOPs in a multidisciplinary lab environment Attend training sessions to learn additional skills 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 your business acumen and profession
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What to Expect Establish an understanding of basic lab practices and SOPs in a multidisciplinary lab environment Attend training sessions to learn additional skills 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 your business acumen and profession
Posted Today
What to Expect Establish an understanding of basic lab practices and SOPs in a multidisciplinary lab environment Attend training sessions to learn additional skills 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 your business acumen and profession
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Receiving and placing calls from and to potential study participants. Enter medical history and demographic information from potential study participants into computerized database. Communicate study information to potential participants. Phone screen participants according to the scripts provided for each study. Schedule screening appointments for potentially qualified participants. Confirm scree
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Serve as site lead for all assigned Phase I clinical studies ensuring that studies are delivered according to Sponsor requirements on time and to high quality. Serves as the primary point of contact for the PM and maintains close and proactive communication with the PM and the clinical team. Provides consolidated comments from the clinical site on the draft study protocol to the Project Manager, t
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Job Overview We have a unique opportunity for an Operations Manager to join our Covance team in San Carlos, CA . This site is a medical device contract research organization. This role provides Oversight and direction on special projects occurring within the business unit including but not limited to equipment and facilities. Assist Site Lead in making important policy, planning and strategic deci
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Covance
- Princeton, NJ / Philadelphia, PA / Austin, TX / 8 more...
Job Overview Responsible for the production of SDTM datasets to the required specification Responsible for the production of TFLs and ADaM datasets to the required specification for clinical, PK, Efficacy and PD reports Responsible for leading studies, ensuring datasets, TFLs and associated documents are completed in a timely and quality manner High level of interaction with external and internal
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A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient's lives. Joining Covance will offer a rewarding career, an opportunity to work in a high energy & collaborative work place, along with access to comprehensive benefits. As an employee your work will be meaningful, the patient outcomes are real, and the results are lasting. Our m
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