FREE ACCESS
5,000–10,000 jobs/day

See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Clinical Research Associate
WEP ClinicalSenior Clinical Research Associate at WEP Clinical overseeing clinical monitoring and site management in compliance with regulatory requirements. Building relationships with sponsors and supporting study-specific procedures.
Posted 5/22/2026full-timeRemote • California, Colorado, District of Columbia, Hawaii, Illinois, Massachusetts, New Jersey, New York, Washington • 🇺🇸 United StatesSeniorWebsite
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Oversee all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs.
- Conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready.
- Build strong relationships with sponsors and sites, serving as a key point of contact throughout the study.
- Support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.
Requirements
What you’ll need- Bachelor’s degree (life sciences, nursing, or related field preferred).
- 5–7+ years’ experience conducting on-site and remote monitoring visits (or equivalent clinical research experience).
- Senior CRA levelling: **SCRA I (3–5 yrs)** – independently manages complex sites; **SCRA II (5+ yrs)** – oversees complex sites/regions, mentors peers, and drives process improvements.
- Broad therapeutic exposure across multiple study types and indications.
- Strong technical/scientific aptitude with the ability to quickly grasp and execute clinical protocols.
- Advanced organizational and logistical skills; able to manage multiple sites/protocols within budget and timelines.
- Excellent written and verbal communication; confident stakeholder engagement.
- Solid understanding of medical/therapeutic areas and medical terminology.
- Proven ability to train, coach, and mentor clinical research staff.
- Proficient with MS Office and EDC systems; willing to travel up to 80%.
Benefits
Comp & perks- Medical, dental, and vision insurance
- FSA, HSA
- Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
- Group short-term and long-term disability insurance
- Group Life Insurance
- 401K safe harbor plan and company match
- Paid vacation, holiday, sick and volunteer time
- Paid maternity & paternity leave
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical monitoringsite managementprotocol adherenceMonitoring Plansclinical research experiencemedical terminologytrainingcoachingmentoring
Soft Skills
organizational skillslogistical skillswritten communicationverbal communicationstakeholder engagement
Certifications
SCRA ISCRA II