CenExel
Location
Broward County, Florida
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various monitoring reports and logs 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 being self-directed, managing shifting priorities across multiple projects, and maintaining exceptional written and oral communication 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.
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.