Clinical Data Manager

The Massey Cancer Center has an exciting opportunity for a Clinical Data Manager - Floater to join the team! Our employees and applicants come from diverse backgrounds. We hire great people from a wide variety of backgrounds, not just because it’s the right thing to do, but because it makes VCU stronger.

Job Description

• Responsible for the collection, entry and management of data for multiple projects from multiple sponsor.
• Engage with study teams and investigators to update, verify, reconcile data
• Focus on data cleanup as a result of data backlog.
• Assist research teams with data entry/corrections in preparation for audits and monitoring visits, as needed.
• Work with the Deep 6 Clinical Research Nurse Analyst to help identify potential patients.
• Inform study teams of Deep 6 identified potential patients to approach at next appointment.
• Assist in study lab kit organization and upkeep.
• Assist in updating and correcting the staff assignments in OnCore at the patient level “on study” tab.
• Proficiency with MS Excel and Word.
• Accurate data entry, word processing, analytical thinking skills.
• Demonstrated ability to work independently and with a team. Excellent organizational and analytic skills, with the proven ability to multi-task, trouble shoot and prioritize work
• Strong attention to detail.
• Effective professional written and oral communications skills (i.e. ability to communication with others in a clear and professional manner).
• Strong interpersonal skills (i.e. ability to work with personnel at all levels to gather information and communicate compliance requirements).
• Ability to learn new programs and electronic information systems.
• Other job duties as assigned.

Minimal Qualifications

Education

• BA/BS degree or degree equivalency with 6 years of experience.
  

Certification/License

• ACRP/SOCRA (or equivalent) certification preferred.

Experience

• 2 years minimum experience in the healthcare or clinical research industry, 4 years preferred.
• Desired: proficient experience with OnCore CTMS, or any other Clinical Trials Management Systems.