CenExel
Location
Decatur, Georgia
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties involve creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution.
Candidates should possess an interest in and knowledge of specific study indications, excellent computer skills, and proficiency in organization and record maintenance. Preferred qualifications include phlebotomy experience and prior experience working with patients, alongside strong initiative and attention to detail.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
1. Indoor, Office environment. 2. Essential physical requirements include sitting, typing, standing, and walking. 3. Lightly active position, occasional lifting of up to 20 pounds. 4. Reporting to work, as scheduled, is essential.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
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