Remote CRA II: Oncology/Ophthalmology

Syneos Health

Iowa (LA)

On-site

USD 85,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Company car
Health benefits
401k match
Stock purchase plan
Bonus eligibility
PTO

Job summary

Syneos Health is seeking a CRA II for Oncology/Ophthalmology in a home-based role serving the Midwestern region. The role involves remote monitoring, site qualification, initiation, data verification, and ongoing site management in compliance with ICH/GCP and GMP guidelines.

You will collaborate with cross-functional teams, prepare for investigator meetings, and support source data verification, IP handling, and TMF alignment. Minimal travel and strong communication are essential.

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
  • Proficient computer skills and ability to adapt to new technologies.
  • Excellent written and verbal communication and interpersonal skills.
  • Ability to travel up to 75% on a regular basis.

Responsibilities

  • Perform site qualification, initiation, monitoring, management and close-out visits (on-site or remote).
  • Ensure regulatory, ICH‑GCP and GPP compliance and escalate serious issues.
  • Verify informed consent, protect confidentiality, and assess data integrity.
  • Review ISF vs TMF, train site staff, and manage tracking of observations and actions.
  • Lead liaison with site personnel and attend sponsor meetings as required.
  • Support audit readiness and contribute to site training and documentation.

Skills

Bachelor's degree / RN
GCP knowledge
Excellent communication
Strong computer skills
Willingness to travel up to 75%
US work authorization

Education

Bachelor's degree
RN qualification

Job description

Syneos Health is seeking a CRA II for Oncology/Ophthalmology in a home-based role serving the Midwestern region. The role involves remote monitoring, site qualification, initiation, data verification, and ongoing site management in compliance with ICH/GCP and GMP guidelines.

You will collaborate with cross-functional teams, prepare for investigator meetings, and support source data verification, IP handling, and TMF alignment. Minimal travel and strong communication are essential.

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