CenExel
Location
Decatur, Georgia
Salary
$53,000 - $55,000 / YEAR
The coordinator ensures the highest standards of data quality and participant safety are maintained, adhering strictly to protocols, SOPs, and regulatory guidelines. Key duties involve assisting the QA Manager with program development, reviewing monitoring reports for trends, and performing ongoing quality reviews of study documentation.
Candidates must possess a minimum of 1-2 years of relevant experience in clinical research and demonstrate in-depth knowledge of FDA regulations, GCP, and ICH guidelines. Essential abilities include strong written and verbal communication, self-direction, flexibility with shifting priorities, and exceptional organizational skills.
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.
$53,000 - 55,000/ year depending on education, experience, and skillset
Ensure that highest standards of data quality and study participant safety are maintained, as well as adherence to study protocols, CenExel SOPs, Site Working Practices (WPs), ICH GCP, Code of Federal Regulations, and IRB Guidelines.
1. Indoor, Office environment. 2. Essential physical requirements include sitting, typing, standing, walking. 3. Lightly active position, occasional lifting of up to 20 pounds. 4. Reporting to work, as scheduled, is essential. 5. On-site work arrangement.
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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