Job Description
Title : Clinical Research Manager Location: Onsite - San Luis Obispo and surrounding sites
Position Summary
This position provides local leadership and day-to-day supervision for clinical trials, research activities, and site-based clinical research staff within assigned regional research sites. The role works closely with key stakeholders (e.g., investigators, research staff, and other internal/external research-related parties) to ensure efficient and compliant research initiation, administration, and support. Additionally, this position facilitates pre-award and post-award clinical trial workflows and recommends improvements for operational efficiency.
Key Responsibilities
Liaison and Guidance:
Act as the central point of contact for the research community.
Provide guidance on research initiation and conduct.
Local Support:
~ Generate support for research activities by maintaining visibility with local leaders, physicians, and patients.
Site Operations Management:
~ Ensure adherence to GCP guidelines, site timelines, quality control, data collection, drug/device management, and staff training.
Resource Management:
~ Monitor staff productivity, clinical trial enrollment, and resource allocation to stay within budget targets.
Data Management:
~ Oversee timely data entry and tracking through CTMS and other research tracking tools.
Quality Assurance:
~ Foster a culture of accountability for quality assurance and continuous improvement.
Training and Development:
~ Develop and implement training materials for site teams.
Standardization and Centralization:
~ Support the standardization of regional research operations and centralize core research support services.
Strategic Planning:
~ Contribute to research operations oversight and strategic planning initiatives.
Qualifications:
Education:
Bachelor’s degree required (life sciences or related field).
Master’s degree preferred.
Licenses & Certifications:
~ SOCRA or ACRP certification required, or eligibility to become certified within one year of hire.
Experience & Knowledge:
Minimum 5 years of full-time experience in clinical trial management in a hospital, clinic, or physician office setting (experience within an integrated health system preferred).
At least 3 years of experience managing and supervising research staff (e.g., clinical coordinators and regulatory staff) or 5 years of leadership experience in the discipline.
Master’s degree may substitute for supervisory experience.
Job Tags
Full time, Local area,
Similar Jobs
Aramark
...therapeutic diets using established protocols and seeks assistance from Supervisor or Dietitian if an error is observed. Assists the clinical staff in ensuring all patients' basic nutrition care needs are met. At Aramark, developing new skills and doing what it takes...
Get It - Marketing
Job Title: Program Manager Job Type: Full-Time Location: Remote (Candidates based in the DC area, Northern Virginia, or Maryland preferred) Salary: Competitive and commensurate with experience About the Role We are a strategic planning consultancy that works...
Randstad US
...medical data entry/ order processer. alpharetta , georgia posted 1 day ago job details summary $18 - $19 per hour temp to perm high school category... ...Qualifications Years of experience: 3 years Experience level: Entry Level Randstad is a world leader in matching great people...
Solomon Page
...and stakeholder engagement. Flexibility to work varied hours in support of event schedules, including evenings for dinners, early mornings for offsite prep, and other event-related support as needed. If you meet the required qualifications and are interested in...
BayMark Health Services
...Employment Opportunity (EEO) and to compliance with all Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, natural origin, ethnicity, religion, gender, pregnancy, marital status, sexual orientation, citizenship,...