Clinical Data Associate

FANTASTIC IMMEDIATE OPPORTUNITY for ENTRY LEVEL & EXPERIENCED candidates

Preference given to candidates with prior clinical research experience

All positions currently hybrid, working 1-2 days/week out of our Boston office.

The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians throughout this process. Great job for someone looking to get back into the workforce.

Duties include:

• Review and evaluation of clinical patient data utilizing the electronic data capture system Medidata Rave®.
• Assisting with the creation and validation of electronic case report forms and edit checks for their assigned studies.
• Using a study specific Data Management Plan, review site reported data elements, generate manual queries, resolve answered queries.
• Perform serious adverse event reconciliation between Rave® and the National Cancer Institute's safety database.
• Review treatment information, evaluate response to treatment, and ensure follow-up and survival data are accurately coded and updated in the database in a timely way.
• Work with the Study Chair to perform final case review. Review and provide input for protocols in development.
• Assist the study chair and statistician with the preparation of the database for analysis.
• Other duties as assigned.

Qualifications:

• Bachelor's degree; preferably in one of the Life Sciences. Medical or biological sciences background is helpful but not required.
• 1+ yr of experience; Previous experience with clinical studies is desired
• Excellent organizational and interpersonal skills
• Proficiency in database and word processing skills, and MS Office
• Excellent written and verbal communication skills
• Strong customer service skills and an ability to interact cordially with others
• Attention to detail
• Knowledge/experience with electronic data submission a plus, but will fully train qualified candidates.

Ideal candidate will have 1+ yr experience with a clinical studies background

All Candidates must submit a cover letter expressing their interest to be considered as well as answering the questions posted.

Complete training is provided to qualified candidates. Full time, 40 hour position, Monday - Friday during normal business hours (8-4 or 9-5).

The ECOG-ACRIN Medical Research Foundation (EAMRF) serves as the grantee organization for the ECOG-ACRIN Cancer Research Group (Group). As a unique nonprofit organization, the overarching mission is to improve and increase patient awareness as well as facilitate access and promote participation in adult oncology clinical trials. The EAMRF provides the necessary support for EA to coordinate the scientific, administrative, governance and membership activities of the Group.

The EAMRF provides the support required to conduct oncology clinical trials. All the trials conducted under the auspices of the Group benefit public health by improving the quality and standard of care of patients with cancer. In addition, the organization promotes collaboration across the scientific community and encourages engagement of patient advocacy at all levels.