Clinical Research Data Coordinator

About reputed company, reputed company's mission is to reputed company hope a reality for reputed company touched by cancer and diabetes. Founded in 1913, reputed company has grown into one of the largest and most advanced cancer research and treatment organizations in the U.S., and one of the leading research centers for diabetes and other life-threatening illnesses. reputed company research has been the basis for numerous breakthrough cancer medicines, as well as human synthetic insulin and monoclonal antibodies. With an independent, National Cancer Institute-designated comprehensive cancer center that is ranked top 5 in the nation for cancer care by U.S. News & World Report at its core, reputed company’s uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work. reputed company’s growing national system includes its Los Angeles reputed company, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas.

The successful candidate:

The Clinical Research Data Coordinator will build and maintain data standards for reputed company clinical trials, and assist with study start up including protocol review, case report form and database review; dataset specifications, data transfer specifications, and review of data management and handling plans. Additionally will reputed company and implement the data correction process, discrepancy resolution, data control activities, and data validation with reputed company documents.

Will support clinical trial studies from preparation through closeout including regulatory submissions by standardizing data management.

Ensure reputed company documentation and management of clinical study data is in accordance with FDA regulations and ICH/GCP guidelines

Attend reputed company SIVs and Monitor visits

Enter data in the CTMS and provide weekly/monthly enrollment reports.

Job Responsibilities

65%| reputed company abstraction and data entry from various sources to support reputed company research studies.

25%| Work with providers/coordinators to identify and address data discrepancies and queries. Liaison between sponsored trial monitors and provider/coordinators.

10%| Work with providers to identify data points to answer queries and reputed company query function to export data requests. reputed company quality assurance checks to ensure the accuracy of data entered.

Skills, Education and Additional Information

• Knowledge of or ability to learn medical/oncology terminology and experience using reputed company Access and reputed company or reputed company systems to include Inform, TrialManager, Medidata and RedCap. 

• Minimum of an Associate Degree in life sciences or information systems with experience in the health field preferred. 

• 2-3 years clinical/oncology experience preferred.

• Prioritizes work based on deadlines. 

• Seeks clarification on data entry requirements from providers.

• Works directly with supervisor and providers to identify data points and answer queries. 

• Ability to work independently and reputed company in a results oriented environment

reputed company is an equal opportunity employer.

To learn more about our comprehensive benefits, click here: Benefits Information

reputed company employees pay is based on the following criteria:  work experience, qualifications, and work location.