OmniSeq is seeking an experienced data manager to support a growing molecular diagnostics evidence development program. The successful candidate will be responsible for meticulous capture, fidelity and management of clinical, outcome and specimen data from external collaborators for multiple studies.

 

RESPONSIBILITIES

• Develop and deploy study data management plans and procedures including collection, organization, coding and storing data for analysis.
• Verify biospecimen receipt and labeling, perform submission and tracking of research sample and associated clinical data in laboratory information system (LIMS).
• Design and manage study specific databases using internal and external data sets.
• Perform all aspects of data capture (electronic and paper), entry and quality control.
• Perform and document data cleaning, transformation, and conformation procedures across multiple primary and secondary sources (medical record, imaging, cancer registry, billing, and laboratory).
• Act as a point of contact for external specimen providers for clinical studies.
• Provide support for preparation of data for analysis and calculation of derived variables.
• Perform complex queries across OmniSeq databases for cohort and sample identification for new studies based on molecular diagnostic test results.
• Setup and maintain project progress dashboard reports.

 

QUALIFICATIONS

• Master’s degree in scientific discipline, preferred epidemiology, public health, or pharmacoeconomics, with at least 3 years’ direct experience preferred. Bachelor’s degree with extensive relevant experience considered.
• Experience managing oncology endpoints/outcomes data
• Ideal candidates will be highly proficient in RDMBS and able to facilitate query resolution with study collaboration staff and internal investigators.
• Excellent verbal and written communication, organizational, analytical, project management and multitasking skills are required.
• Experience designing and managing REDCap and Access databases, strong data quality management skills, and experience with oncology clinical trial endpoint and outcome measurement data highly desired.
• Experience with ethics/human subjects, and regulatory requirements.
• Strong interpersonal skills, positive outlook, and ability to work in a team environment is necessary.

 

To apply, please submit your resume to Jenna Murray, Operations Manager and Human Resources Coordinator at jenna.murray@omniseq.com