Research Site Manager
Providence, United States · On-site · Full-time
- Posted 1mo ago
- From Iterative Health’s careers page
- Location
- Providence, United States
- Work mode
- On-site
- Type
- Full-time
- Level
- Senior
- Experience
- 3+ years
- Department
- Business Operations
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Opens the listing on job-boards.greenhouse.io
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About the role
Where You’ll Drive Impact
- Manage day-to-day activities across research site(s), including staff management, problem-solving, and operational planning.
- Create and implement standardized, well-documented clinic workflows that drive operational excellence and support site goal achievement.
- Attend all site selection visits and site initiation visits (SIVs).
- Oversee inventory of study supplies and ensure adequate stock levels at all times.
- Manage site-level purchasing and expenses in line with cost guidelines and profitability goals.
- Act as assigned or backup CRC as needed to manage team workloads while prioritizing site leadership responsibilities.
- Own the full employee lifecycle for site staff (CRCs and RAs), including hiring, onboarding, assignments, development, performance reviews, and offboarding.
- Ensure timely completion of tasks in EMR and CTMS by CRCs and RAs.
- Lead onsite training of clinical operations staff, including onboarding and study initiation visits.
- Monitor timelines and address issues when performance standards are not met.
- Review, approve, and submit timesheets.
- Work closely with Iterative Health management to develop strategies to meet performance targets around study enrollment, timeliness, and overall site health.
- Meet assigned productivity and quality metrics; meet regularly with coordinators to ensure they meet goals and escalate systemic barriers to the Iterative Health central team.
- Follow up on all monitoring visit action items in a timely manner.
- Maintain effective and ongoing communication with CROs and sponsors.
- Work closely with Principal Investigators and referring physicians to build understanding and enthusiasm for research opportunities for patients.
- Maintain effective communication between site staff, Principal Investigators, and Iterative Health management, including conducting regular site research meetings to discuss study progress and enrollment.
- Identify and manage appropriate third-party vendors; partner with the central Iterative Health team to ensure contracts are fully executed prior to study activation.
- Protect the rights and welfare of all human research participants involved in research.
- Cooperate with Iterative Health research compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
- Assess problem situations to identify causes, gather and process relevant information, generate possible solutions, and make recommendations to management.
- Performs related duties as requested
What You Bring to the Team
- Bachelor's degree from an accredited institution; science disciplines (biology, chemistry, etc.) preferred, or an equivalent combination of education and experience.
- Minimum 3 years of experience as a senior Clinical Research Coordinator; some management experience preferred.
- Strong written and verbal communication skills.
- Ability to read, interpret, and apply clinic policies and research protocols.
- Proficiency in standard office software; experience with EMR and CTMS platforms preferred.
- Highly organized with the ability to manage multiple priorities and meet deadlines with or without direct supervision.
- Strong problem-solving skills and ability to make sound decisions under pressure.
- Ability to interact professionally with staff, investigators, sponsors, and cross-functional partners.
- Willingness to travel across facility sites and occasionally to company meetings.
Preferred Qualifications
- GI and hepatology clinical trial experience.
- Prior experience in a site management or team leadership role within a clinical research environment.
- Familiarity with Iterative Health tools including CTMS, EMR systems, and Salesforce.
- Experience working within a research site network or multi-site clinical trial environment.
- Knowledge of GCP guidelines and human subject research regulations.
How We Work
- Collaborative and low-ego team environment
- High ownership and accountability culture
- Fast-paced and highly iterative growth environment
- Open communication and continuous learning mindset
- Mission-driven organization focused on improving patient outcomes
- Comfortable navigating evolving business priorities and opportunities
Skills they ask for
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About Iterative Health
Clinical research connected to communitiesIterative Health connects research sponsors and clinical research sites to expand access to clinical studies and accelerate development of therapies.
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