Clinical Research Coordinator - Full-time / Part-time

Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, 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.

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 (CRC) 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.

Responsibilities associated with this position:

• 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
• 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
• 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
• Coordinates CRF activities as appropriate; i.e.: Oversees completion of case report forms, CRF documentation and data queries
• 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.

• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)

• In lieu of a degree, typically 3 years’ experience in related field (e.g. pharmaceutical, laboratory, data analysis) will be considered in addition to the experience requirement
• Typically 1-2 years of professional work experience, must include clinical research or related experience
• Basic knowledge of computer and programs (e.g. Microsoft Word, Excel)
• Knowledge of drug development process, ICH Guidelines and GCP