(Contract) Sr. Clinical Research Associate (Sr. CRA)

Therapeutics Inc.; San Diego (CA); On-site; USD 100,000 - 125,000; Full time

Job summary

An innovative company is seeking a dedicated Sr. Clinical Research Associate to manage clinical study sites effectively. In this contract role, you will ensure subject safety and protocol adherence while supporting regulatory submissions. Your expertise in clinical trial monitoring and communication will be vital as you collaborate with diverse teams and mentor junior CRAs. This role offers competitive hourly compensation and the opportunity to make a significant impact in the field of dermatology research. If you are detail-oriented and passionate about advancing clinical research, this is the perfect opportunity for you.

Qualifications

• 3-5 years of clinical trial monitoring experience required.
• Knowledge of clinical research principles and drug development.
• Willing to travel 60-80% for site management.

Responsibilities

• Manage clinical study sites ensuring safety and compliance.
• Monitor sites for protocol adherence and data accuracy.
• Develop and maintain relationships with investigators.

Skills

Clinical trial monitoring

Communication skills

Multitasking

Detail-oriented

Problem-solving

Education

Bachelor’s degree in a scientific field

RN or BSN

Tools

Microsoft Office

Virtual meeting tools

Job description

(Contract) Sr. Clinical Research Associate (Sr. CRA)

Join to apply for the (Contract) Sr. Clinical Research Associate (Sr. CRA) role at Therapeutics Inc.

Founded in 1997, built on 25+ years of dermatology-specific experience, we are the only full-service dermatology CRO that takes products from concept to approval. Voted one of San Diego’s Top Workplaces, we value collaboration, diversity, and dedicated talent. When you join Therapeutics, your contributions are valued and impactful.

Who Are You?

You are passionate, detail-oriented, and a team player who believes in doing quality work. You communicate clearly, collaborate well, and can problem-solve independently.

Primary Objective:

Manage clinical study sites to ensure subject safety, protocol adherence, and compliance with timelines and budgets, supporting regulatory submissions.

Main Responsibilities:

• Assess clinical site suitability.
• Initiate sites with training on protocols and study management.
• Monitor sites for safety and compliance.
• Verify data accuracy against source documents.
• Collect CRFs and queries.
• Write monitoring reports and ensure test article accountability.
• Manage site close-out and audit preparations.
• Develop and maintain investigator relationships.
• Assist with protocol, CRF, and source document development.
• Ensure regulatory and internal guideline compliance.
• Support final report and SOP development.
• Coordinate supplies and project communications.
• Mentor junior CRAs as needed.

Qualifications:

• Based near a major metro area with airport access.
• Bachelor’s degree in a scientific field, RN, BSN, or equivalent, with 3-5 years of clinical trial monitoring experience.
• Knowledge of clinical research principles and drug development.
• Excellent communication and multitasking skills.
• Detail-oriented and able to meet deadlines.
• Proficient with Microsoft Office and virtual meeting tools.
• Willing to travel 60-80%; 85-100% availability preferred.

Position Details:

This is a contract role with compensation between $70/hr and $100/hr, DOE.

We promote an inclusive environment and encourage all qualified candidates to apply.

Additional Info:

• Seniority level: Mid-Senior level
• Employment type: Contract
• Job functions: Research, Analysis, IT