Job description

Articularis Healthcare Group, Inc (AHG) is a physician led and owned organization dedicated to improving the healthcare by supporting independent rheumatology practices across the country. As the nation’s largest rheumatology specialty group with 20+ practices across 7 states, AHG provides access to best business practices, advisory and management services, and value-based treatment pathways.

Articularis Healthcare Group is seeking to add an experienced Clinical Research Coordinator (CRC) to our Summerville, SC. The candidate will work closely with our team of physicians and research coordinators to help execute Rheumatology clinical trials at our Gainesville, GA office.

Job Duties and Responsibilities:

Under the direction and supervision of the Clinical Research Manager, the CRC is responsible for:

• Coordinating and managing multiple investigational study protocols. The CRC will assume a primary role in:
• Reviews, comprehends and develops a familiarity with the investigational study protocols
• Conducts or participates in the informed consent process with study participants
• Screens and enrolls eligible study participants in an efficient and timely manner
• Performs study procedures in accordance with GCP and OSHA guidelines (lab draws/processing, vital signs, EKG, subcutaneous injections, dispense study medications, manage and monitor the use of study electronic devices, etc.)
• Collects data and documents procedures as required by the protocol. Assures timely completion of Case Report Forms, query resolution, and database lock deadlines.
• Prepares and submits IRB reports and maintains regulatory documents compliance with the help of the Clinical Research Regulatory Coordinator (including but not limited to: serious adverse events, protocol deviations, screening logs, database updates, and annual renewal reports)
• Maintains all study records in accordance with sponsor requirements and facility policies.
• Maintains effective and ongoing communication with sponsor, research participants and investigators during the study.
• Coordinates and prepares for monitor / audit visits
• Works effectively and cooperatively with colleagues to provide back-up coordination as required
• Maintains adequate inventory of study supplies
• Assists with orientation of new employees.
• Other duties including travel to Investigator meetings

Required Skills and Qualifications:

Our CRC(s) enjoy a dynamic and challenging job that offers a host of opportunities for growth and career development. The ideal candidate will possess:

• A bachelor's degree in chemistry, biology, or other natural, life or health care science and at least one year of strong, investigational drug studies experience. An associate degree and three years of strong, relevant research experience may be substituted for the required experience.
• A knowledge of clinical research terminology, research documentation, informed consent process, regulatory / IRB submission, and Good Clinical Practice (GCP)
• A proven track record of detail-orientation and high level of performance and accuracy.
• Ability to work well independently and effectively within a team dynamic. Conduct daily operations with minimal supervision and maintain a flexible work schedule.
• Ability to multi-task and set priorities against deadlines.
• Ability to exercise judgment and discretion. Strong critical thinking and problem solving.
• Ability to effectively communicate, both written and verbally
• Strong computer software knowledge and skills
• Excellent interpersonal skills and professional demeanor
• Patience, compassion, enthusiasm, and a strong desire to help humankind through advances in clinical research

Desired Qualities:

• Assertive, self-motivated, passionate and able to learn new things
• Accountable, takes ownership of projects, follow-up and follow through
• Success driven through personal pride
• Commitment to personal and professional excellence
• Team player. Understands quality and produces efficiency and repeatable quality work.
• Learns from mistakes. Follows directions well
• Willing to give and accept positive criticism/feedback without being defensive.
• Must be efficient and conscientious in delivering medical care to patients.
• Must have awareness of patient confidentiality

Work hours: Monday -Thursday. Closed on Fridays! We pay a competitive salary that considers both your experience and your fit with our facility. Full time benefits include PTO, 6 paid holidays, 401k, pension plan, health, dental, long and short term disability, and life insurance.

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 10 hour shift

Ability to commute/relocate:

• Summerville, SC 29486: Reliably commute or planning to relocate before starting work (Required)

Work Location: One location

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