Actalent
Clinical Research Coordinator
We are seeking an onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Vaccine clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. Key Responsibilities: 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. Medical Record Retrieval: Obtain necessary medical records for the study. 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. Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders. General Support: Assist with any other study-related efforts as deemed necessary by the site. Qualifications: Minimum of two years of experience as a Clinical Research Coordinator Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system Pay and Benefits The pay range for this position is $25.00 - $35.00/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 Hammond, LA. Application Deadline This position is anticipated to close on Oct 2, 2025.
We are seeking an onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Vaccine clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. Key Responsibilities: 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. Medical Record Retrieval: Obtain necessary medical records for the study. 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. Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders. General Support: Assist with any other study-related efforts as deemed necessary by the site. Qualifications: Minimum of two years of experience as a Clinical Research Coordinator Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system Pay and Benefits The pay range for this position is $25.00 - $35.00/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 Hammond, LA. Application Deadline This position is anticipated to close on Oct 2, 2025.