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Clinical Trials Associate Jobs in Alabama (NOW HIRING)

Tennessee Oncology

Enroll patients in clinical trials through recruitment, screening, enrollment, treatment, and ... An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing ...

MSD

Good understanding and working knowledge of clinical research, phases of clinical trials, current ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

Good understanding and working knowledge of clinical research, phases of clinical trials, current ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

Good understanding and working knowledge of clinical research, phases of clinical trials, current ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Temple University

$120K/yr

... Research Associates, Clinical Research Coordinators, Research Specialists, and Research ... trials monthly. *Attend site initiation visits to provide management oversight. *Attend site ...

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Clinical Trials Associate information

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$15

$36

$63

How much do clinical trials associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trials associate in Alabama is $36.24, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $39.86 per hour, depending on experience, location, and employer.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

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

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

What cities in Alabama are hiring for Clinical Trials Associate jobs?

Cities in Alabama with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Alabama as of August 2026, with employment types broken down into 2% As Needed, 79% Full Time, 12% Part Time, 1% Temporary, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $75,384 per year, or $36.2 per hour.

Certified Medical Assistant/Patient Care Associate

OneOncology LLC

Huntsville, AL

$16.75 - $21.75/hr

Full-time

Posted 11 days ago

OneOncology rating

7.9

Company rating: 7.9 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

Job description

Clearview Cancer Institute is north Alabama's leading cancer treatment facility. For over 30 years Clearview Cancer Institute has provided leading-edge treatment and compassionate care to those diagnosed with cancer or blood disorders. Clearview offers every service and amenity needed in an outpatient setting and our dedication to research and involvement in Phase I-IV clinical trials gives our patients the opportunity to receive potentially life-saving treatment options.

Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description:

Job purpose

The purpose of the Certified Medical Assistant/Patient Care Associate - Urology is to provide clinical and administrative support to ensure the efficient operation. You will support doctors and patients through a variety of tasks related to patient care management and communicate with accuracy, quality and timeliness.

Essential Job Functions

  • Take and record vital signs and EKG
  • Room patients
  • Prepare patients for examination
  • Obtain and update patient medication
  • Administer Injections
  • Authorizing prescription refills as directed by physicians
  • Assist In Vasectomy , Cystoscopy and Biopsy Procedures.
  • Cleaning and Sterilizing Surgical Instruments.
  • Clinical Supply inventory
  • Collect Urine/Blood Specimens
  • Surgical Scheduling
  • Prior Authorizations for medications and radiology
  • Refills, Lab Orders, Lab results
  • PAT's in Progress
  • Utilize EMR System, Microsoft Teams, Excel and Additional Hospital EMRs
  • Customer Service (greet patients and engage with providers/staff/vendors)
  • Check In/ Check Out
  • Clerical duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without notice.

Education/Experience

  • High School diploma or equivalent
  • Medical office experience (1 year preferred)
  • Certified Medical Assistant
  • BLS Cert
  • Proven working experience as a medical assistant or medical secretary (1 year preferred)
  • Knowledge of medical office management systems and procedures
  • Excellent written and verbal communication skills
  • Strong organizational and planning skills

Working conditions

Work environment involves exposure to potentially dangerous materials and situations that require extensive safety precautions and may include the use of protective equipment.

Physical requirements

Position requires moderate physical effort, standing/walking for more than 75 percent of the day, as well as lifting objects that weight up to 10 pounds. Position may include helping to lift/arrange patients.

Direct reports

This is not a supervisory position.

What OneOncology employees say

Pay

Benefits

Hours and flexibility

Workplace

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