Data Coordinator

START Research; San Antonio (TX); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

401(k) match

Annual performance bonus

Paid time off

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA/HSA plans

Collaborative, growth-oriented culture

Job summary

START Center for Cancer Research invites a Data Coordinator to join our San Antonio team. The role focuses on collecting, entering, and transmitting clinical data for investigational drug studies, with emphasis on accurate CRF completion and data integrity.

Work hours are Monday–Friday, 7:30 a.m.–4:00 p.m. On-site location at 4383 Medical Dr, San Antonio, TX. Collaboration with study teams and compliance with regulatory standards are essential to success in this role.

Qualifications

• High School Diploma or GED required.
• Minimum 2 years of clinical data entry experience.
• General office administration skills and computer applications.

Responsibilities

• Collect, enter/transcribe, and transmit/submit clinical data for assigned studies.
• Receive and request patient records/data to complete CRFs.
• Review patient data for completeness and accuracy.
• Coordinate and schedule monitor visits, including exit meetings.
• Identify labs and coordinate with Regulatory Affairs for lab certifications.
• Review protocols and ensure data entry is current.
• Attend study meetings (site initiation, monitor exit, close-out, audit prep).

Skills

Clinical data entry

General office administration

Education

High School Diploma/GED

Bachelor’s degree

CCR or CCRC credentials

Job description

The START Center for Cancer Research ("START") is the world’s largest early 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 are seeking a Data Coordinator. This role will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies.

Work Schedule:

Work Schedule:

Monday - Friday 7:30 a.m. - 4:00 p.m.

Location:

Location:

4383 Medical Dr.San Antonio, Texas78229

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 as required to 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.
• Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
• Review and utilize protocols as guides for study activities for assigned studies.
• Assure that data entry remains current for all assigned studies.
• Attend meetings as required for assigned studies. This includes, but is not limited to, site initiation meetings, monitor exit 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 computer applications, filing systems.

PreferredEducationandExperience:

• 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 coverage and optional insurance options
• 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. START represents the 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 of the most effective cancer drugs in medical history.

Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide.

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.