Clinical Research Associate, Cell Therapy - Mid Atlantic
AstraZeneca · Wilmington, Delaware, United States of America · Global
Clinical Research
Remote
Dentist
Demand80
Career growth74
Healthcare fit74
Remote potential40
5-year outlook
Likely competitive within pharma-sponsored clinical research, with progression toward Local Study Associate Director, Clinical Trial Manager, or study leadership roles. Exact compensation is not stated in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-24
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Dentist
- Rate period
- Hourly
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians with GCP exposure and clinical trial site experience who want a field-based clinical research operations career. Less suitable for those seeking fully remote work or without monitoring/clinical research exposure.
Who should apply
Research nurses, pharmacists, doctors, IMGs, and allied health professionals with site-level clinical trial experience, GCP knowledge, data collection/reporting exposure, and willingness to travel across the Mid-Atlantic. Cell therapy or oncology trial exposure is helpful.
CV angle
Reframe real clinical experience into clinical research language: protocol adherence, informed consent support, adverse event identification and SAE reporting, source documentation, regulatory binder/ISF familiarity, data query resolution, multidisciplinary site coordination, and audit/inspection readiness. Quantify trial support, patient recruitment, or site coordination only where genuinely true.
Skills to highlight
- ICH-GCP compliance
- Site monitoring and site management
- Source Data Review and Source Data Verification
- CRF review and data query resolution
- SAE reporting and patient safety documentation
- eTMF and CTMS documentation
- Regulatory submissions and IRB/EC interactions
- Risk-based quality management and inspection readiness
Role summary
A field-based CRA role at AstraZeneca responsible for selecting, initiating, monitoring, and closing clinical trial sites in cell therapy studies. The CRA ensures sites follow ICH-GCP, study protocols, SOPs, and regulations while managing site performance, data quality, safety reporting, documentation, and audit readiness.
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