CRC Engagement Lead

Apex Skin•Mayfield Heights, OH

About The Position

Apex Skin and the Apex Clinical Research Center is a rapidly growing skincare facility that empowers employees to deliver exceptional patient experiences. We are currently looking for a talented candidate for the role of Clinical Research Coordinator/Engagement Lead. The role is responsible for various tasks associated with clinical study coordination and patient recruitment activities. This is a Salaried, exempt position. This position requires legal authorization to work in the US.

Requirements

BA/BS/AD/High school diploma or equivalency; BS preferred at minimum
Years of experience: 4 or more in related field
Travel requirements: may be required to travel across Apex clinical sites
Trustworthy, independent and self-motivated
Excellent communication skills- both written and verbal
Presentation skills in small groups
Organizational skills- ability to prioritize
Flexibility to meet the needs of the company
Team building attitude

Responsibilities

Assist with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements which may include maintenance of regulatory documents and binders, data management, IRB submissions and communication to study team
Engage and promote Apex Clinical Research across multiple mediums, including written and face to face education of protocols to medical providers to drive patient recruitment.
Responsible for community outreach and engagement of various stakeholders to drive recruitment of eligible patients to research studies
Collaborate with marketing to drive recruitment, as well as champion the brand
Results-oriented with weekly reporting of metrics to senior leadership
Liaison to medical professionals, providing educational support and ongoing follow-up
Relationship-building with relevant stakeholders
Communicate with sponsors, monitors, and research personnel to ensure all aspects of study compliance.
Collaborate with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
Complete regulatory documents, data capture and other source documentation.
May be required to attain and maintain clinical competencies such as phlebotomy, vital signs, ECG, POC testing, photography and other testing as required.
Assist with preparation for audits, on site monitoring visits, pre study visits, and other sponsor visits to site.
May assist in the development and maintenance of research tools, such as spreadsheets, records, CTMS, etc.
Develop and maintain professional relationships, strong interpersonal skills, including frequent and open effective communication with stakeholders.
May participate in the conduct and documentation of the informed consent process.
May assist in prescreening activities, including chart review, patient intake interviews, phone conversations, and communication with company stakeholders, this includes reaching out to various network providers for the purpose of identifying eligible patients for current studies.
Maintain various Registries with minimal oversight (Psoriasis and Atopic Dermatitis Registries)
Other duties, as assigned.