Clinical Team Lead; Oncology

About the Company

Valkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading oncology multi‑site clinical research network with expertise in oncology. Founded by Dr. David Berz, VCT spans several sites across California and now Denver, Colorado.

Flourish Research is 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 — everyone deserves the best care regardless of race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status.

Clinical Team Lead – Oncology (Denver, Colorado)

LOCATION
:
Onsite

FLSA
:
Non‑Exempt

HOURS
:
Monday to Friday, Day Shift, 40 hours per week

COMPENSATION
: $43.27 – $52.88 per hour (depending on experience)

We are actively hiring a Clinical Team Lead to support our Valkyrie Clinical Trials Denver site, working closely with nursing, pharmacy, laboratory, regulatory, budgets, contract personnel, principal investigators, sub‑investigators, and study sponsors/CROs.

• Represent Flourish in a professional and courteous manner when interacting with staff, sponsors/CROs, IRBs, patients/subjects, nurses, medical staff, and physicians.
• Ensure maintenance of confidentiality and HIPAA compliance for participant/patient information.
• Execute duties in coordination with a Senior CRC as needed.
• Coordinate multiple and complex protocols and guide day‑to‑day activities of the team.
• Follow and enforce SOP compliance for all team members.
• Assist in the review, development, and implementation of SOPs.
• Lead study conduct, including accurate and timely data entry into EMR, EDC, CTMS, and other required systems.
• Provide feedback to the Site Director on team and organizational performance.
• Help with hiring, performance management, talent planning, and termination decisions.
• Educate, mentor, and provide orientation and ongoing training for Clinical Research staff.
• Assist the Site Director with coordination of team members’ daily and weekly schedules to maintain adequate staffing.
• Act as backup for team members during absences or heavy workload periods.
• Schedule and attend meetings such as pre‑Site Selection Visits, SIVs, CRA/Monitor visits, periodic team meetings, and trainings.
• Communicate written and oral information to the team’s performance and any issues requiring intervention.
• Participate in study start‑up, conduct, and close‑out of assigned studies.
• Review charts for accuracy prior to randomization or screen failures.
• Oversee data collection and entry to ensure data integrity.
• Maintain quality control reviews of completed work.
• Ensure prescribed supplies, lab kits, and other study‑specific materials are stocked and valid.
• Track enrollment goals and ensure they are met.
• Assist with budget and contract matters during study creation and amendments.
• Work with the regulatory department to ensure accurate informed consent documents and related records.
• Maintain vital communication channels with Medical Director/Lead Investigator, Site Director, and other team and department leaders.
• Ensure continuous high‑level involvement by principal investigators per FDA, ICH, and SOP requirements.
• Attend meetings and training as required by Site Director, Regional Director, or General Manager.
• Perform additional duties as assigned by management.

• Work performed in a typical interior/office environment.
• Local travel and occasional interstate or international travel.
• Exposure to human bodily fluids.
• Laboratory procedures to obtain and process specimens.
• Participant/patient care responsibilities.
• Daily computer use.
• Occas…