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Weekend Clinical Trials Jobs in Alabama (NOW HIRING)

Houston Methodist

$24 - $32/hr

Five years of clinical research-related experience LICENSES AND CERTIFICATIONS Required * Must have one of the following: CCRC - Certified Clinical Research Coordinator (ACRP)CCRP - Certified ...

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Weekend Clinical Trials information

What is the difference between Weekend Clinical Trials vs Part-Time Clinical Research Coordinator?

AspectWeekend Clinical TrialsPart-Time Clinical Research Coordinator
CredentialsTypically requires clinical trial experience, basic medical knowledgeRequires certification in clinical research or related field, experience preferred
Work EnvironmentConducted at research sites, hospitals, or clinics during weekendsOffice-based, overseeing trial activities, often flexible hours
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, clinical trial sites
Search & Comparison IntentUnderstanding weekend trial roles, flexible clinical trial workPart-time research coordination, clinical trial management

Weekend Clinical Trials involve participating in or managing clinical studies during weekends, often at research sites. Part-Time Clinical Research Coordinators oversee trial activities, ensuring compliance and data collection, usually during regular hours but on a part-time basis. Both roles support clinical research but differ in schedule, responsibilities, and required credentials.

What are the most commonly searched types of Clinical Trials jobs in Alabama?

The most popular types of Clinical Trials jobs in Alabama are:

Weekend Clinical Trials jobs near you

Clinical Research Coordinator Auburn AL

Medovation Clinical Research LLC

Auburn, AL • On-site

$22 - $28/hr

Part-time

Medical, Dental, PTO

Posted 19 days ago

Key responsibilities

  • Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.

  • Analyze data collected during trials and maintain accurate records for compliance management.

  • Oversee blood sampling procedures and ensure proper handling and documentation.

Job description

Benefits
Competitive salary
Dental insurance
Health insurance
Paid time off
Training & development
About Us
We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role.
Role Overview
Here's an opportunity to work for a dynamic and growing clinical research company. We have a fantastic and supportive work environment. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies. This position works on-site at the physician’s practice. This position requires a detail-oriented individual with a strong background in medical terminology, data management, and clinical trials management. The ideal candidate will have at least two (2) years of experience coordinating all aspects of clinical research projects from initiation to completion. Phlebotomy skills required. 
Key Responsibilities
Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
Analyze data collected during trials and maintain accurate records for compliance management.
Oversee blood sampling procedures and ensure proper handling and documentation.
Train on clinical trial protocols and procedures.
Collaborate with healthcare professionals to ensure participant safety and integrity of data.
Utilize software for data capture and reporting
Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders.
Ensure compliance with ethical standards and regulatory requirements throughout the research process.
Required Qualifications
Clinical experience preferred but not required
Experience in Sleep Clinical Trails preferred
Experience in clinical trials 2+ years of coordinator experience
Proficiency in data entry
Knowledge of medical terminology relevant to clinical research.
Phlebotomy and blood sampling techniques is required
Patient Recruitment experience required
Excellent organizational skills with attention to detail and the ability to manage multiple tasks simultaneously
What We Offer
A mission-driven and collaborative team culture.
Opportunities for career growth as the company scales.
The chance to contribute meaningfully to expanding access to clinical research for underserved populations.
If you’re looking for an opportunity to take ownership, build something from the ground up, and make a significant impact, we’d love to hear from you!
Compensation: $22.00 - $28.00 per hour
Medovation Clinical Research is an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. We value impactful work, open collaboration, and a spirit of diversity and inclusion.