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Senior Clinical Research Associate

3+ years
Not Disclosed
10 Feb. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research Associate
Location: Deerfield, IL, USA
Requisition Number: 605
Remote Opportunity

Company Overview:
Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience, and innovation. Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions.

This position can work remotely anywhere in the United States.


What’s in it for YOU?

  • Competitive Compensation: Comprehensive medical, vision, and dental benefits package.

  • Paid Holidays: 10 paid holidays, including a Floating Holiday for a religious or cultural holiday of your choice.

  • Volunteer Time Off: 8 hours of additional PTO to volunteer for a charity of your choice, with up to $120 paid to your charity for your commitment.

  • Wellness Reimbursement: Up to $50 per month for fitness and wellness memberships.

  • Tuition Reimbursement: Up to $5,000 per year.

  • Visibility and Recognition: Direct interaction with Senior Leadership for positive contributions to the business.

  • Team Culture: Opportunity to have a voice and be a part of a very close-knit team offering mentorship, advice, and reliable partnerships.

  • Additional Perks: And more!


Responsibilities:

  • Ensure clinical trials are conducted in compliance with protocol/amendment(s), ICH GCP, SOPs, and applicable regulatory requirements in the assigned countries and sites.

  • Monitor subject safety and verify diligence in protecting the confidentiality and well-being of study subjects.

  • Verify adequacy, completeness, reliability, and quality of trial data collected at study sites.

  • Conduct site qualification, site initiation, interim monitoring, and close-out visits.

  • Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently.


Qualifications:

  • Bachelor’s degree preferred; a Registered Nurse (RN) may also be considered.

  • Minimum of 3+ years of clinical monitoring experience.

  • Ability to travel up to an average of 80%, depending on project needs.

  • This role may be office and/or home-based/field-based; however, regular infrequent visits to a company office will also be required.

  • Current passport or identity card with a valid driving license required.


Commitment to Diversity & Inclusion:

At Advanced Clinical, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. A diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness. Diversity strengthens the legitimacy and relevance of Advanced Clinical in delivering services to our clients. We seek talented, creative individuals from a variety of backgrounds and cultures to work with us. It is our priority that our workplace be inclusive, welcoming of diverse ideas, and appreciative of valuable experience.


How to Apply:

Interested candidates can apply by visiting our careers page or submitting their resume and cover letter directly to Advanced Clinical.

Join us and help drive innovation in clinical research!