Clinical Research Coordinator
Responsibilities
- Oversee the smooth running of clinical trials.
- Perform clinic visits as per the protocol, GCP, and FDA guidelines.
- Complete procedures such as phlebotomy.
- Collect and enter data obtained for the trial.
- Inform participants about study objectives.
- Administer questionnaires.
- Monitor research participants to ensure adherence to study rules.
- Adhere to research regulatory and ethical standards.
- Maintain detailed records of studies as per FDA guidelines and regulatory documentation.
- Manage investigational medication including receiving, dispensing, storing, and performing accountability.
- Liaise with laboratories to process, ship and ensure investigators review reports.
- Participate in subject recruitment efforts.
- Ensure that necessary supplies and equipment for a study are in stock and in working order.
- Engage with subjects, understand their concerns, and manage the visit flow as indicated in the protocol.
Essential Skills
- 1-3 years experience as a Clinical Research Coordinator.
- Phlebotomy experience required.
- Attention to detail.
- Exceptional interpersonal skills.
- Good computer and technical skills.
- Outstanding written and verbal communication.
- Excellent organizational skills.
- Willingness to continually self-educate.
- Bilingual in Spanish is a must.
About the Role
We are seeking a dedicated and skilled Clinical Research Coordinator to join our team in Dallas to support sponsor-led trials in Dermatology. In this role, you will engage with research investigators, pharmaceutical companies, and contract research organizations, as well as research subjects. Your role will require excellent interpersonal and communicative skills to ensure the smooth running of clinical trials.
Job Type & Location
This is a Contract to Hire position based out of Dallas, TX.
Pay and Benefits
The pay range for this position is $28.00 - $33.00/hr.
Requirements
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Dallas, TX.
Application Deadline
This position is anticipated to close on Jul 17, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
San Francisco Fair Chance Ordinance
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector
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