CRA II, Onc/Neuro/Rare/Derm- West Coast

Premier Research; United States; Remote; USD 72,000 - 88,000; Full time

Job summary

Premier Research is seeking a CRA II to monitor Oncology, Neurology, Rare Disease, and Dermatology studies from the West Coast. You will conduct site visits, ensure data integrity, and manage TMF/eTMF while collaborating with global teams to meet regulatory requirements.

The role requires 2+ years in clinical trials, CRA training, and strong ICH/GCP knowledge. Travel is substantial; intense coordination and proactive problem-solving are essential to success.

Qualifications

• Bachelor's degree or international equivalent in clinical, science, or health field.
• 2+ years of clinical trials experience and CRA training completed.
• Strong regulatory knowledge: ICH/GCP, FDA/EU/local regulations.
• Global collaboration and stakeholder management experience.
• Self-directed with strong time management and multitasking.

Responsibilities

• Conduct monitoring visits (qualification, initiation, interim, close-out).
• Ensure data integrity and patient safety per protocol and ICH GCP.
• Maintain TMF/eTMF and review site documents.
• Communicate with study sites, teams, and management.
• Handle administrative tasks like expense submission and hours entry.
• Support feasibility and recruitment, act as SME for additional responsibilities.

Skills

Clinical trials

CRA training

ICH/GCP knowledge

Team collaboration

Education

Undergraduate degree in clinical, science, or health-related field

Licensed healthcare professional (RN)

Tools

eTMF familiarity

Data management systems

Job description

Premier Research is looking for a CRA II, Onc/Neuro/Rare/Derm- West Coast to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here.

What You'll Be Doing:

• Conducts all monitoring visit types (qualification, initiation, interim, close-out; remote/onsite) per the Clinical Monitoring Plan, ensuring data integrity, patient safety, and quality/timeliness of deliverables and reports, while planning and prioritizing day-to-day site activities
• Ensures validity, correctness, and completeness of clinical data per ICH GCP/ISO14155, protocol, and client requirements; manages query resolution with sites and Data Management
• Maintains TMF/eTMF per ICH/GCP Appendix C and organizational filing guidelines, reviewing site documents for accuracy and completeness; reviews IP accountability and logs as directed
• Manages communication with study sites, project teams, and management, including Investigators' Meetings and required internal/study-specific training and therapeutic knowledge-building
• Handles administrative responsibilities: timely expense submission, time/hours entry, project tracking, site visit metrics, and confidentiality/compliance with global and local laws
• Proactively supports the project: reduces backlog, assesses feasibility/recruitment as needed, acts as a resource/SME for other CRAs, may take on additional country- or project-specific responsibilities, and performs other duties as assigned

What We Are Searching For:

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
• 2+ years’ experience in clinical trials and proven previous success as a CRA required, completion of CRA training program
• Strong regulatory/clinical knowledge: ICH/GCP, FDA/EU/local regulations, ISO14155, drug/device development, and clinical monitoring procedures, plus relevant clinical/health systems and cultural/regional knowledge for assigned markets
• Proven leadership and collaboration: experience coaching/mentoring CRAs, strong team player, full-time availability to internal/external stakeholders, and global experience preferred
• Self-directed and organized: excellent time-management skills, self-starter with sound judgment, able to multitask and adapt in a fast-paced, changing environment
• Accountable and customer-focused: dependable with strong commitment, applies consistent performance standards, decisive problem-solver, and customer-service oriented internally and externally

Travel: 70-85%

Lifting up to 25lbs

Valid driver's license, passport as required

Experience required in Oncology, Rare Disease, Neurology, or Dermatology

To be considered for this position, you must be located in one of the following regions: West Coast, Midwest, Northeast.

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized minimum base pay for this role is $80,000 USD. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status.