Clinical Site Manager

About Rare Disease Research:

As an independent clinical research site, we are 100% dedicated to conducting clinical research, accelerating the development of safe and effective treatments and providing rare disease patients with access to innovative investigational therapies. We are a passionate, caring, multi-disciplinary team conducting clinical research with expertise and compassion, and always to the highest ethical standards.

About This Opportunity:

We are looking for a Clinical Site Manager to join our team of researchers in our Atlanta location. The ideal candidate will have Senior Clinical Research Coordinator Experience and strong management skills. •

Important Note:

Applicants for employment in the United States must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States and with Rare Disease Research.

Responsibilities:

Oversee daily operations of a clinical research site, ensuring compliance with protocols, regulatory requirements, and sponsor expectations Manage and mentor clinical research staff, including coordinators and assistants, to maintain high performance and professional development Ensure adherence to

ICH-GCP, FDA

regulations, and internal SOPs across all active studies Have a working knowledge of all studies at Atlanta RDR site Serve as a resource for the clinical team to navigate through study protocols, and to prepare and navigate additional new studies Attend all study meetings to help clinical staff manage and prioritize study projects and tasks If required, ability to serve as primary CRC for studies to provide direct oversight and mentorship for junior staff Coordinate closely with investigators, often assisting with patient visits, scheduling, and protocol execution Assist the clinical team with communications with monitors, CRAs, and other internal and external parties to ensure clinical trial activities are completed on time and on budget Supports quality assurance with study documents to ensure studies are conducted effectively and with strict adherence to study protocols Directly manages Research Assistants (RA) and their work to assist their growth to becoming Clinical Research Coordinator (CRC) Identify and mitigate operational risks, protocol deviations, and compliance issues Develop and implement process improvements to increase efficiency and data quality Ensure proper training and onboarding of new staff on protocols, SOPs, and systems Supports staff offboarding, ensuring any remaining tasks are identified and covered This list is not exhaustive and additional duties may be added due to company needs

REQUIREMENTS

Bachelor's degree in clinical related field, post-secondary degree preferred 6 - 8 years experience in the clinical research field, including management of clinical research teams. Detail-oriented, excellent verbal and written communication skills. Certification from CRP from SOCRA or ACRP Please note that due to the immunocompromised nature of our patients COVID and flu vaccinations are

REQUIRED

Notice To Third-Party Agencies:

Rare Disease Research does not accept unsolicited resumes from recruiters or agencies. Any staffing/employment agency, person or entity that submits an unsolicited resume to this site does so with the understanding that the applicant's resume will become the property of Rare Disease Research will have the right to hire that applicant at its discretion and without any fee owed to the submitting staffing/employment agency, person, or entity. Work Remotely No, this position is full-time in-person

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance

Job Type:

Full-time Pay:

$85,000.00 - $120,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance

Experience:

Management:

3 years (Preferred) Clinical trials management: 6 years (Preferred)

License/Certification:

CCRC with SOCRA or ACRP (Preferred) Ability to

Relocate:

Brookhaven, GA 30329: Relocate before starting work (Required)

Work Location:

In person