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Snr. Clinical Research Associate - Remote

CyberCoders

Arlington Heights (IL)

Remote

USD 90,000 - 120,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a Senior Clinical Research Associate to lead clinical trials and ensure regulatory compliance. In this pivotal role, you will manage site monitoring activities, collaborate with regulatory authorities, and develop essential documentation to support clinical studies. This position offers a competitive salary and benefits, along with the opportunity to make a significant impact in the field of clinical research. If you have a passion for advancing healthcare and possess strong project management skills, this is the perfect opportunity for you to thrive in a dynamic environment.

Benefits

Health Insurance
Dental Insurance
Vision Insurance
401(k)
PTO/Vacation

Qualifications

  • 6-10 years of clinical research experience required.
  • Expertise in oncology or infectious diseases preferred.

Responsibilities

  • Oversee clinical trials ensuring compliance with ICH-GCP guidelines.
  • Lead site selection and monitoring visits, ensuring timely issue resolution.

Skills

Clinical Research
Regulatory Compliance
Site Monitoring
Project Management

Education

Bachelor's degree in Life Sciences
Nursing
Pharmacy

Job description

Snr. Clinical Research Associate - Remote

This range is provided by CyberCoders. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$90,000.00/yr - $120,000.00/yr

Senior Clinical Research Associate (CRA)

We are seeking an experienced Senior Clinical Research Associate (CRA) to oversee and ensure the successful execution of clinical trials. This role requires expertise in site monitoring, regulatory compliance, and stakeholder collaboration.

Key Responsibilities

  • Maintain and ensure the accuracy of the Trial Master File (eTMF).
  • Lead site selection, initiation, monitoring, and closeout visits.
  • Ensure compliance with ICH-GCP guidelines, ethical regulations, and sponsor protocols.
  • Collaborate with Ethics Committees (ECs) & Regulatory Authorities (RA) for approvals.
  • Develop and maintain monitoring plans, issue reports, and training materials.
  • Identify risks, implement CAPA plans, and ensure timely resolution of study issues.
  • Review CRA visit reports and escalate quality or compliance concerns as needed.
  • Support audits, inspections, and provide site personnel training.
  • Travel up to 50% as required.
Qualifications
  • Bachelor's degree in Life Sciences, Nursing, or Pharmacy (required).
  • 6-10 years of clinical research experience.
  • Expertise in oncology, rare diseases, infectious diseases, cardiology, or neurology.
  • Experience with Phase I-II and First-in-Human (FIH) trials preferred.
  • Strong project management and regulatory compliance knowledge.

This is an exciting opportunity for a detail-oriented CRA to make a meaningful impact in clinical research. Apply today!

Benefits

Competitive Base Salary
PTO/Vacation
Health, Dental, Vision Insurance
401(k)

Email Your Resume In Word To

Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
brianna.lancaster@cybercoders.com

Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : BL8-1847216 -- in the email subject line for your application to be considered.

Brianna Lancaster - Recruiter

For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.

This job was first posted by CyberCoders on 04/02/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.

CyberCoders is proud to be an Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please contact a member of our Human Resources team to make arrangements.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Research, Analyst, and Information Technology

Industries

Pharmaceutical Manufacturing

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