What are the responsibilities and job description for the Clinical Research Coordinator position at MaximaTek?
Job Requirement: Clinical Research Coordinator (CRC) – Entry Level
Job Title: Clinical Research Coordinator (CRC) – Entry Level
Location: Texas, United States
Job Type: Full-Time
Experience: 0–3 Years (Freshers & Recent Graduates are encouraged to apply)
Job Summary
We are seeking a highly motivated and detail-oriented Entry-Level Clinical Research Coordinator (CRC) to join our clinical research team in Texas. The candidate will support clinical trials by coordinating study activities, maintaining accurate documentation, ensuring regulatory compliance, and assisting investigators with patient-related procedures.
Key Responsibilities
- Assist in planning, coordinating, and managing clinical research studies.
- Recruit, screen, and schedule eligible study participants.
- Explain study procedures and assist with informed consent documentation.
- Collect and accurately maintain patient and clinical trial data.
- Maintain source documents, regulatory binders, and study records.
- Ensure compliance with study protocols, ICH-GCP guidelines, FDA regulations, and institutional policies.
- Coordinate patient visits, laboratory samples, and study procedures.
- Communicate effectively with Principal Investigators (PIs), sponsors, and study participants.
- Report adverse events, protocol deviations, and study updates to the research team.
- Assist during sponsor visits, audits, and regulatory inspections.
Required Qualifications
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, Biochemistry, Public Health, or a related healthcare field.
- Basic understanding of clinical research and clinical trial processes.
- Strong verbal and written communication skills.
- Excellent organizational and documentation skills.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Ability to work independently and as part of a multidisciplinary team.
Preferred Qualifications
- Clinical Research Certification (CRC/CCRC, GCP training) is a plus.
- Internship, academic project, or healthcare experience preferred but not mandatory.
- Knowledge of medical terminology and electronic data capture (EDC) systems is an advantage.
Required Skills
- Attention to detail
- Time management
- Patient interaction and communication
- Data entry and documentation
- Problem-solving skills
- Ability to maintain confidentiality and professionalism
Compensation & Benefits
- Competitive salary package
- Medical, dental, and vision insurance
- Paid time off (PTO) and holidays
- Clinical research training and mentorship
- Career growth opportunities within the clinical research industry
Interested candidates can apply with their updated resume. Fresh graduates looking to build a career in Clinical Research are highly encouraged to apply.