Bilingual Part Time Clinical Research Coordinator

Job description

Bilingual Part-Time Clinical Research Coordinator
Contract duration: Open-ended contract (typically 3-6 month duration)
Start date: ASAP
Schedule: 24 hours per week (Monday-Friday)
Job Description
Hiring for abilingual clinical researchprofessional to act as a consultant CRC to support am ongoing clinical trial.

The main job duties for this position will be chart review, phone screening and patient recruitment.

This position will help identify patients for enrollment through chart review, patient follow-up and pre-screening.

This individual will be speaking with potential patients over the phone to educate and screen against the study criteria for enrollment.

In addition, he or she will be responsible for educating medical professionals and networking within the medical community for patient referrals.
Responsibilities

+ Patient Recruitment: Identify and recruit suitable patients for the clinical trial.

+ Medical Record Review: Conduct thorough reviews of patient medical records.

+ Participant Screening: Perform phone screenings or prescreen participants for eligibility.

+ Informed Consent: Obtain informed consent from trial participants.

+ Data Management: Collect study data and enter it into electronic data capture (EDC) systems.

+ Query Resolution: Address and resolve data queries promptly.

+ Medical Record Retrieval: Obtain necessary medical records for the study.

+ Documentation: Create and maintain source documents.

+ Compliance: Ensure compliance with e-diary protocols.

+ Adverse Event Reporting: Assist with timely reporting of adverse events (AEs) and serious adverse events (SAEs).

+ Study Visit Preparation: organizing participant schedules, ensuring informed consent, preparing necessary documentation, and coordinating with the research team to ensure all protocols are followed.

+ Participant Follow-Up: Conduct follow-up with study subjects to ensure retention.

+ Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.

+ Administrative Tasks: Perform various administrative duties as required.

+ Community Outreach: Visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.

+ Referral Physician Networking: Building relationships between clinical researchers and community physicians to facilitate patient recruitment for clinical trials

+ Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store them, perform initial processing like serum separation, and transport them to a lab for further analysis and storage.

+ General Support: Assist with any other study-related efforts as deemed necessary by the site.

Essential Skills

+ Experience with clinical trials and electronic data capture (EDC) systems.

+ Proficiency in query resolution and patient recruitment.

+ Bilingual English/Spanish

+ At least 2 years of experience as a Clinical Research Coordinator.

+ Minimum of 2 years' experience in clinical research and query resolution.

Additional Skills & Qualifications

+ Strong attention to detail and ability to work in a fast-paced environment.

+ Excellent communication and organizational skills.

Pay and Benefits
The pay range for this position is $25.00 - $32.00/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 Cooper City,FL.
Application Deadline
This position is anticipated to close on Nov 4, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Required Skill Profession

Other General