RESEARCH COORDINATOR I at ATLANTA DIABETES ASSOCIATES PC

Atlanta, Georgia, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

0.0

Posted On

05 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Patient Recruitment, Informed Consent, Clinical Trial Documentation, Data Entry, Microsoft Office, Human Subject Protection, IRB Operations, Regulatory Standards, HIPAA Compliance, Interpersonal Communication, Specimen Processing, Organizational Skills

Industry

Medical Practices

Description

Description The Clinical Research Coordinator I will work within a leading endocrinology practice in Atlanta, GA, implementing, managing, and overseeing clinical studies related to diabetes and other endocrine disorders. The coordinator ensures compliance with ICH, GCP, and FDA standards and observes the guidelines set by Atlanta Diabetes Associates. Core responsibilities include patient recruitment, assisting with informed consent, monitoring study progress, and maintaining meticulous documentation for clinical trials. The role involves direct patient interaction, data entry, and managing study inventories. This in-office position may occasionally require evening or weekend hours, depending on project needs, and is ideal for those passionate about advancing endocrine research. Requirements Education/Experience: Prior experience in a medical office, laboratory, or research setting is preferred, with an emphasis on clinical research or endocrinology. Skills: Proficiency in Microsoft Office (Word, Excel, PowerPoint) and general computer use. Understanding of human subject protection, Institutional Review Board (IRB) operations, and regulatory standards. Familiarity with medical and lab equipment and their protocols. Strong attention to detail, organizational skills, and ability to maintain confidentiality, particularly with HIPAA guidelines. Excellent interpersonal skills for effective communication with study participants, investigators, regulatory agencies, and the healthcare team. Adaptability and flexibility to handle changing responsibilities and environments, with the ability to work on multiple projects simultaneously. Commitment to professional growth, with access to ongoing training and development through workshops and seminars. Physical and Schedule Requirements: Job Type: Full-time (40 hr./week) Location: In-office (non-remote) Schedule: Typically follows business hours of 8a-5p, Monday through Friday. Start-End times may vary depending on assigned projects. Occasional weekend and night work required, as assigned by Department managers Physical Requirements: This role requires the ability to move throughout the clinic and laboratory areas, including standing or walking for extended periods. Coordinators should be able to lift and carry materials up to 20 pounds, have manual dexterity for specimen processing and data entry, and clear vision and hearing for reviewing medical records and effective communication. This position may also require extended periods of sitting and computer use, as well as the use of personal protective equipment (PPE) when handling specimens or working with patients. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management retains the right to add or to change the duties of the position at any time.

Responsibilities

The coordinator implements and manages clinical studies related to diabetes and endocrine disorders while ensuring compliance with ICH, GCP, and FDA standards. Key duties include patient recruitment, monitoring study progress, and maintaining meticulous trial documentation.