Full-time
Clinical Research Coordinator - Cancer Research
Competitive
Burbank, CAScience & PharmaceuticalPosted 17d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
17 days ago
Job description
Proforma Health is hiring a Clinical Research Coordinator to support clinical trial activities under supervision. The role involves patient screening and follow-up, study data quality, and collaboration with investigators, sponsors, and clinical research nurses to help complete studies.
Responsibilities
The Clinical Research Associate I supports clinical trial activities under supervision, including patient screening, eligibility assessment, registration, data quality control, study evaluation, and patient follow-up via phone
They collaborate closely with investigators, sponsors, and clinical research nurses to ensure study completion, while maintaining confidentiality, punctuality, and team-oriented conduct
Preferred
certifications like ACRP or SOCRA
oncology or Phase I-II trial experience
familiarity with Electronic Data Capture systems such as InForm or Medidata Rave
ACRP Certification
SOCRA Certification
Oncology Trial Experience
Phase I–II Trial Experience
Electronic Data Capture
InForm
Medidata Rave
Benefits
Comprehensive health coverage
Retirement plans
Paid time off
Additional incentives
Company
Medical billing services for healthcare providers and practices.
Norwalk, CT, US
https://www.proformahealthinc.com/
11-50 employees
Qualifications
a Bachelor's degree or equivalent
at least 1 year of clinical research coordination or data entry experience
A Bachelor's degree or equivalent
At least 1 year of clinical research coordination or data entry experience
Certifications like ACRP or SOCRA
Oncology or Phase I-II trial experience
Familiarity with Electronic Data Capture systems such as InForm or Medidata Rave
Required skills
Clinical Research Coordination, Data Entry, ACRP Certification, SOCRA Certification, Oncology Clinical Trials, Phase I–II Clinical Trials, InForm, Medidata Rave
Preferred skills
certifications like ACRP or SOCRA, oncology or Phase I-II trial experience
Experience
1+ years
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