Job Description

Clinical Site Manager

Location/Onsite: Reno, NV | Onsite

Our client seeks a Clinical Site Manager in the clinical research field to join their team in Reno, NV. This is a full-time, onsite position. Are you a seasoned clinical research professional with a knack for leading teams and driving operational excellence? Do you thrive in fast-paced environments and have a passion for supporting breakthrough research? Are you looking to bring your management experience to a collaborative, growing organization? If yes, this may be the perfect Clinical Site Manager position for you. Keep scrolling to see what this company has to offer.

The Perks!

Compensation: $75,000.00 - $115,000.00/year, based on experience

Benefits information:

• 401(k) + company matching
• Health and Dental Insurance
• Paid time off
• Flexible spending account
• Professional development assistance

A Day in the Life of the Clinical Site Manager

As the Clinical Site Manager, you’ll oversee the full lifecycle of clinical trials, from site initiation and staff training to monitoring and close-out. You’ll lead a dedicated team of clinical research coordinators while ensuring regulatory compliance, participant retention, and enrollment goals are met. Your work will directly support groundbreaking research and help bring new treatments closer to those who need them.

Responsibilities include:

• Managing the full clinical trial cycle: site assessments, initiation, monitoring, subject retention, and close-out
• Directing and training clinical staff on compliance, evaluations, travel, and scheduling
• Ensuring accurate and timely completion of study startup documentation
• Collaborating with leadership on staffing and trial targets
• Communicating effectively with sponsors, investigators, participants, and internal teams
• Developing strategies to meet or exceed enrollment goals
• Overseeing training and compliance with all regulatory requirements
• Supporting investigators and the research team throughout trial execution
• Preparing for and managing sponsor visits, audits, and FDA inspections
• Fostering a supportive and collaborative team culture

Requirements and Qualifications:

• 4+ years of clinical research coordinator experience
• Experience managing clinical trials, review boards, FDA, Regulatory, etc
• At least 2 years of experience managing teams in a clinical research setting
• CCRC certification or equivalent preferred
• Strong knowledge of FDA regulations and ICH-GCP
• Excellent organizational, communication, and problem-solving skills
• Ability to lead, multi-task, and work well across interdisciplinary teams

About the Hiring Company:

Our client is a respected and growing clinical research organization dedicated to advancing medical research through high-quality clinical trials. Known for their strong leadership, collaborative work environment, and commitment to excellence, they’re looking for someone who shares their passion for research and team development.

Come Join Our Clinical Operations Team!

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

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