Clinical Research Coordinator

Highly Competitive Salary
  1. Permanent
  2. Clinical Trial Assistant (CTA), Clinical Research Associate (CRA), Patient Recruitment
  3. United States
Corpus Christi, USA
Posting date: 21 Oct 2020
CR.MJ.33732

Proclinical is currently recruiting for a Clinical Research Coordinator with a leading research facility located in Corpus Christi, TX. As the Clinical Research Coordinator, you will recruit and screen patients for inclusion in protocols/clinical trials.

Job Responsibilities:

  • Perform patient assessments and collect medical histories and physicals.
  • Administer protocol consents and documentation.
  • Monitor protocol compliance.
  • Perform clinical data interpretation and data entry as needed.
  • Oversee training and mentoring of staff.
  • Evaluate and interprets protocol/clinical trial findings.
  • Manage clinical protocols by training the study personnel; oversee compliance to protocol
  • Develop and adhere to relevant SOPs
  • Manage the quality control, completion and submission of study related documentation.
  • Prepare, submit and maintain IRB, FDA, and/or other regulatory documents and research correspondence as needed.
  • Monitor study enrollment goals and initiate strategies to promote enrollment and participant compliance.
  • Coordinate and perform responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, and overseeing study visits.
  • Obtain and document informed consent of participants.
  • Assess acute and non-acute clinical and research related problems and toxicities, communicate to physicians and report adverse events per protocol to sponsor and IRB.

Skills and Requirements:

  • Bachelors degree in nursing, or equivalent experience.
  • 2-5 years' experience required.
  • Expertise in the fundamentals of clinical trials.
  • Experience in clinical data management, database operations and analysis.
  • Experience with IRB and FDA requirements.
  • Certified in GCP and Human Subjects Protection training.
  • Experience in clinical research setting with protocols and clinical trials.
  • Strong diagnostic and clinical skills.
  • Excellent Writing Skills.

If you are having difficulty in applying or if you have any questions, please contact Mary Jacobs at (+1) 312-291-4181 or m.jacobs@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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