Clinical Research Coordinator job in Corpus Christi, USA

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: Clinical Trial Assistant (CTA), Clinical Research Associate (CRA), Patient Recruitment

Location: United States

This vacancy has now expired. Please see similar roles below...

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.

#LI-MJ1

Related jobs

Clinical Research Coordinator

Salary

Highly Competitive Salary

Location:

Philadelphia, USA

Proclinical is seeking a dedicated and enthusiastic Clinical Research Coordinator who is passionate about clinical-translational research in the field of head and neck cancer