Clinical Research Coordinator

Industry

Medical and Nursing

Advert ID

USA_520557

Location

Corpus Christi

Job Type

Contract

Hours

Full-Time

Salary Range

USD30-60/hr

No. of Openings

1

Branch Information

Frederick, MD - Professional - (USA) 7470 New Technology Way (Professional) MD Frederick , MD 21703

ContactNumber

301-694-8921

Job Description

Clinical Research Coordinator

Corpus Christi



Do you have experience with clinical trials/protocols? Do you have a current nursing license? In this Contract opportunity, you'll have the chance to recruit and screen patients for inclusion in protocols/clinical trials; perform patient assessments and collect medical histories and physicals. You'll also:



* 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.



Well qualified applicants will bring:

* Bachelor's degree in nursing

* 2-5 years of related experience

* Current nursing license

* 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



Apply today to learn more about this rewarding Contract opportunity!