Clinical Research Associate I - Immunology (Orlando, FL)
AbbVie · United States · US
Clinical Research
Remote
Nurse
Dentist
Demand80
Career growth82
Healthcare fit82
Remote potential25
Salary band
USD 75k – 143k
5-year outlook
CRA roles in pharma offer structured career progression and competitive compensation that grows with monitoring experience and therapeutic area expertise. Exact figures vary by location and company.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
full-time
Date found
2026-10-28
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- Nurse, Dentist
- Rate period
- Annual
Why this was classified this way
- contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians with clinical research coordination or data management exposure who want to move into pharma-sponsored trial monitoring. Less suitable for those without any clinical research experience.
Who should apply
Nurses, pharmacists, doctors, or allied health professionals with clinical research coordinator or data management experience; IMGs with research backgrounds seeking industry CRA roles.
CV angle
Frame clinical experience around trial coordination, patient recruitment, protocol compliance, data integrity, GCP knowledge, site communication, and any monitoring or audit exposure. Emphasize transferable skills from patient-facing roles such as documentation accuracy, regulatory awareness, and cross-functional collaboration.
Skills to highlight
- Clinical trial monitoring
- GCP/ICH guidelines
- Site management and training
- Patient recruitment and retention
- Data integrity and compliance
- Risk assessment
- Regulatory audit readiness
- Stakeholder communication
Role summary
CRA I responsible for supporting investigative sites in immunology clinical trials through site evaluation, training, monitoring, and closure activities under supervision. Ensures compliance with GCP, protocols, and SOPs while driving data quality and patient safety.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.