Job Description

Clinical Site Manager

Location/Onsite: Portland, OR – In-office

Do you have a passion for leading teams in the world of clinical research? Are you a detail-oriented professional who thrives in managing operations and driving results? If yes, this may be the perfect Clinical Site Manager position for you. Keep scrolling to see what our client has to offer!

The Perks!

• Compensation: $90,000–$130,000 per year depending on experience
• Benefits:
• 401(k) matching
• Flexible schedule
• Health insurance
• Paid time off
• Professional development assistance
• Special Perks: Enjoy a consistent Monday-to-Friday schedule with no nights or weekends.

A Day in the Life of a Clinical Site Manager

As a Clinical Site Manager, you’ll oversee clinical trial operations from start to finish, ensuring compliance, efficiency, and quality at every stage. You’ll lead a dedicated team, foster collaboration, and ensure trials meet enrollment and retention goals. Your work will contribute directly to advancing medical knowledge and improving patient outcomes.

Responsibilities include:

• Managing the full clinical trial lifecycle, including site assessments, initiation, monitoring, and closeout.
• Directing staff activities, including training, compliance, scheduling, and evaluations.
• Ensuring all study startup documentation and timelines are completed.
• Collaborating with the executive team to meet staffing and trial goals.
• Developing strategies for participant recruitment and retention.
• Overseeing training for protocols and regulatory requirements.
• Supporting the team in all trial-related activities, including audits and monitoring visits.
• Creating a supportive and collaborative work culture.

Requirements and Qualifications:

• Minimum of 4 years of clinical research coordinator experience, with at least 2 years in a management role.
• Certified Clinical Research Coordinator (CCRC) or equivalent preferred.
• Strong understanding of FDA regulations and ICH-GCP guidelines.
• Excellent organizational, communication, and problem-solving skills.
• Proficient in relevant clinical systems and software.
• Proven ability to build and maintain strong interpersonal relationships.
• Sound business acumen and attention to detail.
• Experience managing a clinical trial, review boards, FDA, and Regulatory
• Good management skills and leadership abilities (ability to manage a busy schedule of patients and maximize site efficiency)

About the Hiring Company:

Our client, Advanced Research Institute, is a multi-specialty clinical trial company that leads the industry in conducting high-quality research. With a mission to advance medical breakthroughs, they foster a professional and ethical work environment that prioritizes patient care and collaboration.

Come Join Our Clinical Research Team!

Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you!

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