Clinical Research Coordinator

Joulé; Houston (TX); On-site; USD 50,000 - 59,000; Full time

Job summary

A leading staffing company is seeking a Clinical Research Coordinator in the Houston area. This entry-level position involves screening and enrolling study participants while ensuring protocol compliance and data integrity. The successful candidate must exhibit strong organizational skills and communicate effectively with a diverse team.

Qualifications

• Entry-level role with main focus on patient monitoring and data collection.
• Strong skills in communication, organization, and detail orientation preferred.

Responsibilities

• Screen and enroll study subjects ensuring protocol compliance.
• Collect and enter data into study-specific case report forms.
• Maintain accurate records and documentation as required.

Skills

Organizational skills

Detail-oriented

Professional communication

Interpersonal skills

Tools

MS Word

Excel

Job description

Title:Clinical Research Coordinator

Location:Kingwood, TX

Type/Duration:Contract, 6 months

Schedule:Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning starts

Start Date: ASAP



Summary of Key Responsibilities:Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports.



Duties and Responsibilities:



• Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements

• Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance

• Collects, completes, and enters data into study specific case report forms or electronic data capture systems

• Ensures timely and accurate data completion

• Collects blood samples and tracks shipments and requests supplies as needed

• Implements study-specific communications

• Ensures timely adherence to protocol requirements

• Responsible for completion of all required documentation

• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications

• Communicates all study-related issues to appropriate study colleagues or manager

• Apprises principal investigator and management of all study specific medical issues for guidance

• Attends study specific meetings as required or asked to do so

• Reviews and responds to any monitoring findings and escalates issues

• Organizational and prioritizing capabilities

• Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel

• Professional communication

• Communicate and work effectively with a diverse team of professional

• Interpersonal skills, detail-oriented and meticulous

• Work independently in a fast pace environment with minimal supervision at off-site facilities



Ref: #568-Clinical



#M3

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research

• Industries

  Staffing and Recruiting

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