Senior Regulatory Affairs Associate - CTA Senior Specialist
Parexel · United States · US
Regulatory Affairs
Remote
Dentist
Demand78
Career growth72
Healthcare fit72
Remote potential95
5-year outlook
Likely stable to strong within CRO regulatory affairs; senior CTA specialists can progress toward regulatory management or lead roles, but compensation depends on region and prior submission experience. No salary data is provided.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-19
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Dentist
- Rate period
- Annual
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 prior regulatory, CTA, or clinical trial submissions experience who want remote CRO work. It is not ideal for clinicians without regulatory exposure.
Who should apply
Physicians, pharmacists, or healthcare graduates with clinical research, regulatory affairs, or CTA submission experience; research coordinators or nurses transitioning into regulatory roles may also fit if they can demonstrate submission and compliance work.
CV angle
Frame clinical trial, protocol amendment, ethics/IRB, regulatory documentation, compliance, and cross-functional coordination experience using CTA and submission language. Quantify dossiers, timelines, authority queries, and CRO/vendor interactions without inventing regulatory ownership.
Skills to highlight
- CTA submission coordination
- Regulatory dossier preparation
- Health authority interactions
- EU regulatory requirements
- CRO/vendor oversight
- Regulatory compliance
- Cross-functional collaboration
- Regulatory tracking and archiving
Role summary
A remote senior regulatory affairs role at Parexel supporting global Clinical Trial Application submissions, dossier preparation, health authority interactions, CRO oversight, and regulatory compliance for clinical trials.
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