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The START Center for Cancer ResearchPosted 18 days ago

Data Coordinator

Full-time
On-site
2+ years
Competitive
Posted 18 days ago

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

Posted
18 days ago
Source
startresearch.bamboohr.com
Sector
Healthcare

Opens the employer's application page in a new tab

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

Qualifications

  • 2 years of clinical data entry experience
  • Knowledge and training in general office administration skills, including computer applications, filing systems

Preferred

  • 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

Required skills

CCRCCCRP

Nice to have

Bachelor's degreeCCRP or CCRC credentials

Full job description

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

Preferred

  • 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

Benefits

  • 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-paid life and disability insurance
  • Employee Assistance Program (EAP) providing confidential, no-cost support for you and your family from day one
  • Flexible FSA and HSA plans
  • A supportive environment that values balance, wellbeing, and flexibility
  • A collaborative, creative workplace where team members are encouraged to contribute
  • Continuous learning and professional growth
  • Specialized Phase 1 oncology clinical trials provider.
  • San Antonio, Texas, USA
  • https://startresearch.com
  • Late Stage
  • Total Funding
  • unknown
  • 2024-04-03
  • Acquired
  • Leadership Team
  • Chris Takimoto
  • Global Chief Medical Officer
  • Recent News
  • PR Newswire
  • Allegheny Health Network and The START Center for Cancer Research Announce Strategic Collaboration to Expand Patient Access to Early-Phase Cancer Trials
  • 2026-08-25
  • Bizjournals.com Feed (2025-11-12 15:43:17)
  • AHN teams up with START Center to expand early-phase oncology research in western Pennsylvania
  • Baptist Health South Florida and The START Center for Cancer Research Announce Strategic Partnership to Expand Patient Access to Early-Phase Cancer Trials
  • 2026-05-28
  • Company data provided by

Qualifications

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

Required skills

  • CCRC, CCRP, Case Report Form (CRF) Completion

Preferred skills

  • Bachelor's degree, CCRP or CCRC credentials, Familiarity with medical terminology

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 26, 2026

Work mode

On-site

Job source

startresearch.bamboohr.com

Company

The START Center for Cancer Research

Healthcare

See all 9 jobs from The START Center for Cancer Research →
  • New Hyde Park, NY
  • Healthcare

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