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Clinical Research Coordinator

MCRAGreenville, South Carolina, United StatesOnsite
Notice: MCRA’s Talent Solutions division works to untie top talent with opportunities on our clients’ teams.

This posting is not for a position directly at MCRA, but rather for a position with a MCRA client that our team is helping to recruit and fill.


Our client seeking a full-time clinical research coordinator to support ongoing studies. This position will be based in-person at a study site/clinic and will support all trial activities at the site level. The Clinical Research Coordinator will be responsible for coordinating and managing clinical research studies in compliance with institutional, state and federal regulatory guidelines, assist investigators in securing successful study implementations and leading project meetings, while taking part in the data collection and analysis process.

Qualifications:


  • High School Diploma with a field in research or the equivalent combination of education and/or experience
  • Minimum of 2 years’ experience in clinical research setting with experience in phlebotomy (requirement).
  • Demonstrated experience in the daily activities of clinical trials such as subject recruitment, budget preparation, and collection of laboratory specimens
  • Detailed knowledge of FDA, ICH, and GCP guidelines and regulations
  • Excellent interpersonal, organizational, and communication skills
  • Ability to prioritize, manage multiple tasks, and meet deadlines
  • Experienced in Word, Excel, and Outlook

Special Requirements:


  • Onsite position at a doctors office in Greenville, SC
  • Monday-Thursday 9:30am-4:30pm EST
  • Hourly Compensation

NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.MCRA, LLC is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.Apply for this job

Life at MCRA

Musculoskeletal Clinical Regulatory Advisers, LLC (MCRA) is the leading advisory firm to the neuro-musculoskeletal industry with growing experience in other specialties. Founded in 2004, MCRA is headquartered in Washington, DC, with offices in New York, NY, and Manchester, CT, has more than 50 team members, and serves over 400 unique clients globally. The true value of MCRA is the integration of six business value creators for orthopedic & other medical/surgical specialties: regulatory, reimbursement, clinical research, intellectual property, compliance, and quality assurance. MCRA provides “first-in-class” services through its superior knowledge base, global surgeon and physician relationships, and deeply experienced management team. Additionally, MCRA recently started Specialty Healthcare Advisers (SHA), which specializes in healthcare provider consulting. MCRA’s many years of expertise in clinical, reimbursement, regulatory and compliance to provide our clients with a unique 360? integrated perspective. Depending on client needs or goals, MCRA provides clinical trial enrollment strategy and data collection, regulatory strategy, submission and execution, specialty coding & reimbursement recommendations, RAC audit preparedness and defense, Medicare pre-determination assistance, and other services. MCRA’s core clientele are orthopedic spine and biologic medical device companies, private equity firms, CROs, and law firms, and we have an increasing percentage of clientele from other healthcare industries.
Thrive Here & What We Value- Equal opportunity/Affirmative Action employer- Strong professionalism and customer service skills- Effective interpersonal skills</s>
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