Data Coordinator

START Research; West Valley City (UT); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

401(k) retirement plan with employer 1

Annual performance bonus

Generous paid time off

Medical, dental, and vision coverage

EAP program

Flexible FSA and HSA plans

Job summary

START Research in Utah seeks a Data Coordinator to collect, enter, validate, and transmit clinical data for investigational drug studies across START's Mountain Region.

The role requires meticulous data handling, CRF knowledge, and coordination of monitor visits while maintaining regulatory standards. Hours are Monday through Friday, 8 a.m. to 5 p.m., in West Valley City.

Qualifications

• Must have strong data entry capabilities and familiarity with clinical data terminology.
• Experience with case report forms (CRFs) and data quality checks is preferred.
• CCRP or CCRC credentials are a plus.

Responsibilities

• Collect, enter, and transmit clinical data for assigned studies.
• Review data for completeness and accuracy and resolve data queries.
• Coordinate monitor visits and archive study documentation.
• Ensure timely data entry and CRF completion according to protocols.

Skills

Data entry

Medical terminology

Attention to detail

CRF knowledge

Education

High School Diploma/GED

Bachelor’s degree

Tools

EHR systems

Job description

The START Center for Cancer Research (“START”) is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access”tocutting edgetrials throughout the UnitedStatesand Europe.

We areseekingaData Coordinator. This role will collect, enter/transcribe, andtransmit/submitclinical data for assigned investigational drug studies.

Schedule: Monday - Friday 8 a.m. - 5 p.m.

Location: START Mountain Region 2965 W 3500 S #4thWest Valley City, Utah

84119

Essential Responsibilities

• Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
• Receive and request patient records/data from the study team asrequiredto complete CRFs for assigned studies.
• Review patient data for completeness and accuracy for assigned studies.
• Coordinate and schedule monitor visits for assigned studies.This includes exit meetings with monitors to review data or queries.
• Identifylab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
• Review andutilizeprotocols as guides for study activities for assigned studies.
• Assure that data entryremainscurrent for all assigned studies.
• Attend meetings asrequiredfor assigned studies.This includes, but is not limited to, site initiation meetings,monitorexit meetings, close-out visit meetings, and audit preparation meetings.

Education & Experience

• High School Diploma/GED.
• 2 years of clinical data entry experience.
• Knowledge and training in general office administration skills, including computerapplications,filing systems., etc.

Preferred Education and Experience

• Bachelor’s degree.
• Ability to accurately perform data review and CRF completion in its entirety with minimal direction.
• Familiarity with medical terminology.
• CCRP or CCRC credentials is highly desirable.

Best-in-Class Benefits and Perks

• 401(k) retirement savings plan with employer match
• Eligibility for an annual performance bonus, based on role and company results
• Generous paid time off and paid holidays
• Comprehensive medical, dental, and vision coverageand optional insuranceoptions
• Company p‑aid life and disability insurance for added financial protection
• Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one
• Flexible FSA and HSA plans to support your financial wellness
• Commitment to a supportive environment that values balance, wellbeing, and flexibility
• We’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda –one ofthe most effective cancerdrugsin medical history.

Learn more at STARTresearch.com.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.