QC & Data Management Specialist

About Us

FLOURISH RESEARCH is where clinical trials thrive. We are one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At FLOURISH RESEARCH, we strive toward excellence. We embrace employees, customers, and patients from underrepresented groups to help make this vision a reality. We are committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.

Essential Job Functions

• Represent site in a professional and courteous manner (verbal, written and in appearance) when interacting with site staff, sponsors, IRBs, patients/subjects, nursing and medical staff members of various clinics/hospitals and physician offices.
• Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and sponsor protocols. Indicate data points that are missing or discrepant and identify and report any trends to the QC Manager, Team Leads, and upper management.
• Accurately enter data into an eCRF/CRF system according to the sponsor provided eCRF/CRF guidelines in a timely manner. Identify and report missing data points or inconsistencies to the clinical research coordinator and QC Manager, Team Leads, and upper management as soon as possible.
• Attend SIV meetings. Report any discrepancies between the source and CRF/eCRF immediately to the CRC and the QC Manager, Team Leads, and upper management.
• Resolve open queries thoroughly, accurately and in a timely manner. Assist in sponsor monitor visits to resolve queries in a timely manner.
• Possess the ability to work closely with other staff members and sponsor representatives in a professional manner. Assist with training onboarding procedures.
• Perform all duties in a time- and cost-effective manner. Additional duties as assigned by management.

Requirements

• Minimum of 1-3+ years' experience within the field of clinical or biological research.
• Experience: Bachelor's degree or commensurate experience.
• Demonstrates core values & all skills set required.
• Must be experienced with Microsoft office applications (Outlook, Word and Excel) as well as internet-based applications.
• Must be detail oriented, organized, self-motivated, be able to work independently and on a team, and the ability to stay on task.
• Must have good written and verbal skills.
• Must have good critical thinking and problem-solving skills.
• Must be professional and have a strong work ethic.
• Must have the ability to adapt and take-on additional tasks as requested.
• Must have the ability to understand medical terminology and research concepts.
• Demonstrates some knowledge of FLOURISH processes.
• Demonstrates some knowledge of clinical research industry guidelines/regulations.
• Assists with key initiatives/process improvements in the department.
• Assists with training company new hires.
• Completes at least 8% of goals annually.

Benefits

• Health, dental, and vision insurance plans.
• 401(k) with a 100% employer match on the first 4% of employee contributions.
• Tuition reimbursement.
• Parental leave.
• Employee referral program.
• Employee assistance program.
• Life insurance.
• Disability insurance.
• A generous PTO plan covering vacation, sick, personal days and 8 paid holidays.