Clinical Research Coordinator

Covance Inc Located in: Dallas,  Texas
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Do you have experience in Clinical Research? Are you looking for new opportunities? Covance has a job opening for a Clinical Research Coordinator at its Dallas, TX facility.

The Clinical Research Coordinator serves 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. The CRC serves as the primary point of contact for the PM. Maintains close and proactive communication with the PM and the clinical team.

Other Duties and Responsibilities:

• Provides consolidated comments from the clinical site on the draft study protocol to the PM, taking into account operational and subject safety issues

• Perform all aspects of the clinical process to include the development and approval of study schedules, study specific documentation, clinical set-up, resourcing, clinical conduct, delegating tasks as appropriate

• Monitors/maintains participant safety, dignity and compliance, including coordination of appropriate medical consultation/treatment as appropriate. Provides updates regarding participants wellbeing to the investigators and PM

• Work closely and proactively with operational teams to ensure laboratory, equipment and all operational requirements are fulfilled, study is adequately resourced and all personnel are trained and competent on all study procedures. Leads operational team members to ensure staff, supplies and equipment are appropriate

• Keeps the PM and site management aware of deficiencies or potential problems and assists in taking appropriate action in response to issues

• Is fully aware of all regulatory submissions, timelines and approvals and coordinates and ensures submission of documents to the IRB/IEC as appropriate for timely review

• Works with recruiting and screening staff to define a recruiting plan for the trial and to ensure the study is recruited on schedule. Update PM regularly with recruiting and screening information, question and concerns. Reviews participant eligibility information to determine if protocol criterions are met. Communicates with Investigators and PM regarding participant eligibility.

• Coordinates CRF activities as appropriate; i.e.: Oversees completion of case report forms, CRF documentation and data queries. Works with key staff to ensure these items are completed in a timely manner. Oversees transfer of CRF information to appropriate data management individuals

• Ensures biological samples are shipped as appropriate and as directed by the client, in a timely manner

Covance believes that their best-in-class employees deserve first-class benefits. Covance offers an outstanding benefits package including medical & dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, short and long-term disability, and life insurance.

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.



Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.


Seniority Level:
Experienced - Not Management
  R&D / Science
Preferred Industry Background:
Managing a team of:
Required Travel:

Base Salary:
Other Compensation: