Covance Operations Coordinator in Dallas, Texas

Job Description:

Covance has a job opening for an Operations Coordinator at its Dallas, TX facility.

The Operations Coordinator is responsible for logistical set up of studies; to ensure good study flow and adequate resources are assigned.

Responsibilities & Duties:

  • Assists the Clinical Research Coordinator with their responsibilities and acts as their back-up as needed

  • Assists in creation of source documents, labels and study specific instructions

  • Assists in creation of study schedules

  • Orders supplies/equipment and dietary needs for assigned studies

  • Assists in staff training of study specific procedures

  • Coordinates tasks related to participant check in and discharge and may assist with resolution of participant issues

  • Completes sample shipment documentation as necessary

  • Compiles data tables/summaries as requested.

  • Assists with the compilation of protocol and SOP deviations

  • Maintains an understanding of FDA, GCP and ICH requirements

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.

Requisition ID: 70246BR

Job Category: Clinical Research

Locations: United States - Dallas, TX

Shift: 1

Job Postings: Covance has a job opening for an Operations Coordinator at its Dallas, TX facility.

The Operations Coordinator is responsible for logistical set up of studies; to ensure good study flow and adequate resources are assigned.

Responsibilities & Duties:

  • Assists the Clinical Research Coordinator with their responsibilities and acts as their back-up as needed

  • Assists in creation of source documents, labels and study specific instructions

  • Assists in creation of study schedules

  • Orders supplies/equipment and dietary needs for assigned studies

  • Assists in staff training of study specific procedures

  • Coordinates tasks related to participant check in and discharge and may assist with resolution of participant issues

  • Completes sample shipment documentation as necessary

  • Compiles data tables/summaries as requested.

  • Assists with the compilation of protocol and SOP deviations

  • Maintains an understanding of FDA, GCP and ICH requirements

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.

Education/Qualifications: • 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).

o In lieu of a degree, typically 1 years experience in related field (e.g. pharmaceutical, laboratory, data analysis) will be considered in addition to the experience requirement.

Experience: • Typically 6-12 months of professional work experience. Experience in clinical research is preferred.

• Basic knowledge of computer and programs (e.g. Microsoft Word, Excel).

• Knowledge of drug development process, ICH Guidelines and GCP.

EEO Statement:

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.