Job Description

CLINICAL RESEARCH COORDINATOR Job Description  Collaborates with both the clinical team and physicians (principal investigators) to strategically and effectively conduct clinical trials  Serves as a liaison between the clinical team, the patient, family and the pharmaceutical company during the patient's participation on the clinical trial  Ensures data quality and integrity during each phase of data collection of industry studies  Demonstrates responsibility for the accuracy and integrity of all clinical trials through the maintenance of both paper and computerized records of experimental procedures and outcomes  Updates supervisor, principal investigators, sponsors or cooperative groups with important research study information including study progress updates, new toxicities, or serious adverse events  Ensures that serious adverse events are documented completely and reported to all appropriate parties  Ensures that all regulatory documents (amendments, continuing review, deviations, etc) are updated and submitted to the appropriate parties including the study sponsor  Participates in the study development and start-up process including reviewing protocols, designing and/or reviewing continuous review forms, preparing informed consent forms, developing study documents and submitting to the appropriate parties.  Performs other duties as assigned. Additional Skills & Qualifications MINIMUM EDUCATION: Bachelor's degree in a health related field, required MINIMUM EXPERIENCE : 3 years prior experience in a clinical setting. Pay and Benefits The pay range for this position is $26.93 - $38.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Harlingen,TX. Application Deadline This position is anticipated to close on Nov 3, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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Temporary work,

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