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Clinical Research Consulting Jobs (NOW HIRING)

Actalent

Clinical Research Nurse

Mobile, AL · On-site

$25 - $35/hr

Clinical Research Nurse - Mobile, AL Hours: 20 hours per week CLINICAL RESEARCH EXPERIENCE ... With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and ...

Vitalief

Clinical Research Nurse

New Brunswick, NJ · On-site

ABOUT VITALIEF Vitalief is a consulting and professional services firm that partners with clinical research sites, sponsors, and CROs to enhance trial activation, operational performance, and ...

Actalent

Clinical Research Nurse

Mobile, AL · On-site

$25 - $35/hr

Clinical Research Nurse - Mobile, AL Hours: 20 hours per week CLINICAL RESEARCH EXPERIENCE ... With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and ...

Actalent

Clinical Research Coordinator

Lancaster, CA · On-site

$25 - $35/hr

Clinical Research Coordinator Hours: 36 hours per week Contract: 6 months This Clinical Research ... With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and ...

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Clinical Research Consulting information

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$49K

$107.3K

$189K

How much do clinical research consulting jobs pay per year?

As of Aug 10, 2026, the average yearly pay for clinical research consulting in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals in clinical research consulting, and how can they be addressed?

Clinical Research Consultants often encounter challenges such as navigating complex regulatory requirements, balancing the needs of multiple stakeholders, and adapting to changing study protocols. Staying current with regulatory updates, maintaining clear communication with clients and research teams, and developing strong organizational skills are key strategies for overcoming these challenges. Additionally, consultants benefit from building a robust professional network to share insights and best practices, which helps ensure study compliance and successful project delivery.

What is clinical research consulting?

Clinical research consulting involves providing expert guidance and support to organizations or investigators conducting clinical trials and research studies. Consultants help with protocol development, regulatory compliance, study design, data management, and ensuring that research follows ethical and legal standards. They play a key role in optimizing study processes, navigating complex regulations, and improving the quality and efficiency of clinical research projects.

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

To thrive as a Clinical Research Consultant, you need a strong background in clinical research methodologies, regulatory compliance, and a relevant life sciences degree—often complemented by experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and data analysis tools is typically required. Exceptional communication, problem-solving, and organizational skills help consultants build client trust and navigate complex regulatory environments. These competencies are crucial for ensuring ethical, efficient, and successful research outcomes that meet both client expectations and industry standards.

What is the difference between Clinical Research Consulting vs Clinical Research Associate?

AspectClinical Research ConsultingClinical Research Associate
CredentialsTypically requires a degree in life sciences, clinical research certifications (e.g., CCRP, CCRA)Requires a degree in life sciences; certifications like CCRA or RAC are common
Work EnvironmentConsultants often work independently or with consulting firms, providing expert advice to multiple clientsWorks directly on clinical trial sites or with sponsors, monitoring trials
Employer & Industry UsageUsed by consulting firms, CROs, or as independent contractors in the clinical research industryEmployed by pharmaceutical companies, CROs, or clinical trial sites

While both roles require similar educational backgrounds and certifications, Clinical Research Consulting involves providing expert advice and strategic guidance across multiple projects, often independently. In contrast, a Clinical Research Associate focuses on monitoring and managing specific clinical trial sites to ensure compliance and data integrity.

More about Clinical Research Consulting jobs
What cities are hiring for Clinical Research Consulting jobs? Cities with the most Clinical Research Consulting job openings:
What states have the most Clinical Research Consulting jobs? States with the most job openings for Clinical Research Consulting jobs include:
What job categories do people searching Clinical Research Consulting jobs look for? The top searched job categories for Clinical Research Consulting jobs are:
Clinical Research Consulting jobs near you
Infographic showing various Clinical Research Consulting job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Nurse

Actalent

Mobile, AL • On-site

$25 - $35/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 days ago

Job description

Job Title: Clinical Research Nurse - Mobile, AL
Hours: 20 hours per week
CLINICAL RESEARCH EXPERIENCE & REGISTERED NURSE LICENSE REQUIRED
Job Description
This part-time Clinical Research Nurse role offers an opportunity for a nursing professional to support an clinical trial at a dedicated research site in Mobile, AL. The Clinical Research Nurse will work closely with patients and the research team to ensure safe, accurate, and compliant execution of study activities, including patient screening, visit coordination, and clinical procedures.
Responsibilities
  • Pre-screen patients for enrollment by reviewing medical records and evaluating eligibility against study inclusion and exclusion criteria.
  • Schedule patient appointments and coordinate visit logistics in alignment with the clinical trial protocol and site processes.
  • Perform detailed medical record reviews to collect and verify relevant clinical data for the study.
  • Navigate and utilize the electronic medical record (EMR) system to access patient information, document study-related data, and maintain accurate records.
  • Attend and support patient study visits, ensuring all protocol-required procedures and assessments are completed correctly and on time.
  • Perform blood draws and related specimen collection in accordance with clinical standards and study requirements.
  • Educate patients on study medications, including proper usage, potential side effects, and adherence expectations, while reinforcing informed consent and patient understanding.
  • Support patient recruitment and enrollment efforts by communicating study information clearly and professionally to potential participants.
  • Collaborate with the research team to maintain high-quality data, ensure protocol compliance, and uphold patient safety throughout the trial.
  • Maintain attention to detail in all documentation, data entry, and patient interactions within a fast-paced research environment.
Essential Skills
  • Minimum of 2 years of experience as a Clinical Research Nurse, Registered Nurse (RN), or Licensed Practical Nurse (LPN).
  • Direct experience working in oncology, preferably within a clinical or research setting.
  • Proficiency with electronic medical record (EMR) systems, including navigation, data entry, and chart review.
  • Demonstrated ability to conduct thorough chart reviews and extract relevant clinical information accurately.
  • Experience with patient enrollment and recruitment for clinical studies or healthcare programs.
  • Competence in performing blood draws and handling specimens according to clinical standards.
  • Strong patient education skills, with the ability to explain medications and study procedures clearly.
  • High level of attention to detail and accuracy in documentation and data management.
  • Ability to work effectively in a fast-paced clinical research environment while managing multiple tasks.
Additional Skills & Qualifications
  • Experience in oncology nursing or experience supporting oncology patients in a clinical setting.
  • Strong organizational and time-management skills to coordinate multiple patient appointments and study tasks.
  • Effective communication skills to interact with patients, families, and the research team..
  • Professional nursing licensure as an RN or LPN in good standing, consistent with local regulations.

Work Environment
This is a part-time contract position (approximately 20 hours per week) for a duration of about 7 months, based on-site at a clinical research facility in Mobile, AL. The role follows normal business hours and operates in a fast-paced environment that requires strong attention to detail, accurate documentation, and consistent adherence to clinical research protocols.
Job Type & Location
This is a Contract position based out of Mobile, AL.
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 hybrid position in Mobile,AL.
Application Deadline
This position is anticipated to close on Aug 16, 2026.
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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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About Actalent

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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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