Clinical Research Registered Nurse

About MPact Clinical Research

At MPact Clinical Research, we are dedicated to advancing human health through innovative Clinical Research. Our mission is to contribute to generalizable knowledge about human health and illness, while testing methods that improve our ability to prevent, diagnose, and treat diseases. Located in Northwest Houston, our state-of-the-art facility is equipped to conduct clinical trials aimed at enhancing patient care and outcomes.

Clinical Research Coordinator, On-Site

· Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.

· Clinical skills experience with patients to obtain vitals and possibly perform procedures such as blood draws, EKGs, etc.

· Knowledge and experience of site operations and the drug development process

· Effective communication

· Computer proficiency in use of Microsoft Word, Excel

· This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials.

· The employee, working closely with study team members, will achieve study objectives and corporate goals.

· Ability to coordinate as primary CRC on at least 1-3 studies of low to medium complexity, with oversight by a manager or higher-level CRC.

· May assist as backup CRC on other studies.

· Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved.

· Obtains informed consent of research subjects.

· Develop strong working relationships and maintain effective communication with study team members.

· Completes all protocol-related training.

· Performs patient/research participant scheduling.

· Collects patient/research participant history.

· Collects and maintains source documentation.

· Manages inventory and administers test articles/investigational product to participants.

· Performs data entry and query resolution.

· Supports the collection and review of required essential study documents and reports.

· Order supportive study supplies (e.g., contracts, IXRS ( to manage patient enrollment, patient randomization, and study drug supplies), lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)

· Adheres to an IRB-approved protocol.

· Supports the safety of research subjects, and report adverse events.

· Coordinates protocol-related research procedures, study visits, and follow-up

· Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close-out activities.

· Collects, processes, and ship laboratory specimens.

· May be asked to perform special project responsibilities and travel to other CCT locations when needs arise.

· Complies with MPact, Clinic, and Sponsor policies, standard operating procedures (SOPs), and guidelines.

· Performs other duties as assigned.

The actual base pay offered may vary based on several factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule.

Job Type: Full-time

Pay: $55,000.00 - $60,000.00 per year

Benefits:

• 401(k)
• Paid time off

Standard shift:

• Day shift

Weekly schedule:

• Monday to Friday

Ability to Relocate:

• Houston, TX 77090: Relocate before starting work (Required)

Work Location: In person