Clinical Research Coordinator

Overview

Direct message the job poster from Maxima Tek

Maxima Tek partners with top-tier healthcare organizations and research institutions to connect exceptional recent graduates and experienced professionals (0-5 years) with high-impact, full-time clinical roles. We specialize in placing talent where it can truly thrive, with a strong focus on Clinical Trial Management, Regulatory Compliance, and Patient Data Integrity. Our expertise and network help us place candidates in environments where they can excel and develop their careers in the life sciences.

Clinical Research Coordinator

We are actively seeking motivated individuals for Entry-Level and Mid-Level full-time Clinical Research Coordinator positions. Responsibilities focus on the daily operations of clinical trials, ensuring that studies are conducted according to protocol, budget, and regulatory requirements. This includes recruiting and screening participants, maintaining essential study documents, and ensuring the accuracy of clinical data collection.

• Manage daily operations of clinical trials to ensure protocol adherence, budget compliance, and regulatory requirements.
• Recruit and screen participants; maintain essential study documents; ensure accuracy of clinical data collection.

• Education: Hold a Bachelor’s or Master’s degree in Life Sciences, Biology, Public Health, Nursing, or a similar healthcare-related discipline (Required).
• Experience: Possess 0-5 years of relevant work experience in a clinical setting, laboratory, or healthcare environment.
• Technical Skills (Required):
• Solid understanding of Good Clinical Practice (GCP) and FDA regulations
  .
• Experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Veeva, or Oracle).
• Proficiency in maintaining Trial Master Files (TMF) and processing Informed Consent Forms (ICF).
• Strong familiarity with HIPAA regulations and patient privacy standards.
• Preferred Skills (Clinical Specific):
• Experience with patient recruitment, screening, and enrollment processes.
• Knowledge of medical terminology and standard laboratory procedures (phlebotomy experience is a plus).
• Familiarity with Institutional Review Board (
  IRB
  ) submission processes.
• Proficiency in Microsoft Office Suite and clinical project management tools.
• Certifications: Certified Clinical Research Coordinator (
  CCRC
  ) or Certified Clinical Research Associate (
  CCRA
  ) is a strong plus.

• Targeted Placement: Direct, high-volume marketing of your profile to our extensive network of hiring managers specializing in Clinical Trials, Biotech, and Pharmaceutical research.
• Expert Resume Rebuild: Personalized refinement of your resume to make it competitive and optimized for the Clinical Research and Life Sciences ecosystem.
• Career Guidance: Dedicated support and guidance to help you navigate behavioral interviews and regulatory knowledge assessments.

Email your updated resume to:

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Consulting
• Industries: IT Services and IT Consulting

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