Shriners Children's
Clinical Research Program Manager
Shriners Children's, Portland, Oregon, United States, 97204
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Clinical Research Program Manager
role at
Shriners Children’s
Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid‑sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multidisciplinary education, and research with global impact. We foster a learning environment that values evidence‑based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.
All employees are eligible for medical coverage on their first day! Upon hire all employees are eligible for a 403(b) and Roth 403(b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a full‑time or part‑time status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short‑term and long‑term disability and Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected. Additional benefits available to full‑time and part‑time employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and more. Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.
Schedule: Full time 1.0 FTE
Responsibilities
Accountable for the site's research activities. Facilitates the local site's research programs and projects through collaborative, timely communications and teamwork.
Works effectively with SHC leadership to ensure the research mission is upheld. Maintains a contemporary knowledge of clinical research regulatory requirements.
Takes a leadership role in implementation of process development and improvement changes, as needed.
Provides support, direction, supervision and mentoring for any site clinical research coordinators promoting exemplary study conduct, subject safety, and the generation of accurate and complete substantiated data within SHC's data safeguards.
Has an extensive working knowledge of the complex clinical research process, from protocol development to implementation, including experience with clinical trials.
Supports the implementation of approved research protocols, ensures studies are conducted in compliance with the approved protocol.
Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study.
Safeguards all participants involved in a research study supported and approved by Shriners Children's, maintains patient safety and privacy throughout the study.
Note: This is not an all-inclusive list of this job's responsibilities. The incumbent may be required to perform other related duties and participate in special projects as assigned.
Required Qualifications
Without a Bachelor's degree, 5 or more years of specific job‑related experience in the administration of clinical research.
3 or more years Clinical research experience, e.g. experience with site management, study management, IRB's, and federal regulations regarding clinical research compliance.
Preferred Qualifications
Bachelor's in Clinical Research, science or other healthcare related field.
Master's in Clinical Research, science or other healthcare related field.
Experience in the coordination of intergroup or multi‑site clinical studies.
CCRP or CCRC certification.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Project Management and Information Technology
Industries Hospitals and Health Care
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Clinical Research Program Manager
role at
Shriners Children’s
Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid‑sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multidisciplinary education, and research with global impact. We foster a learning environment that values evidence‑based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.
All employees are eligible for medical coverage on their first day! Upon hire all employees are eligible for a 403(b) and Roth 403(b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a full‑time or part‑time status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short‑term and long‑term disability and Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected. Additional benefits available to full‑time and part‑time employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and more. Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.
Schedule: Full time 1.0 FTE
Responsibilities
Accountable for the site's research activities. Facilitates the local site's research programs and projects through collaborative, timely communications and teamwork.
Works effectively with SHC leadership to ensure the research mission is upheld. Maintains a contemporary knowledge of clinical research regulatory requirements.
Takes a leadership role in implementation of process development and improvement changes, as needed.
Provides support, direction, supervision and mentoring for any site clinical research coordinators promoting exemplary study conduct, subject safety, and the generation of accurate and complete substantiated data within SHC's data safeguards.
Has an extensive working knowledge of the complex clinical research process, from protocol development to implementation, including experience with clinical trials.
Supports the implementation of approved research protocols, ensures studies are conducted in compliance with the approved protocol.
Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study.
Safeguards all participants involved in a research study supported and approved by Shriners Children's, maintains patient safety and privacy throughout the study.
Note: This is not an all-inclusive list of this job's responsibilities. The incumbent may be required to perform other related duties and participate in special projects as assigned.
Required Qualifications
Without a Bachelor's degree, 5 or more years of specific job‑related experience in the administration of clinical research.
3 or more years Clinical research experience, e.g. experience with site management, study management, IRB's, and federal regulations regarding clinical research compliance.
Preferred Qualifications
Bachelor's in Clinical Research, science or other healthcare related field.
Master's in Clinical Research, science or other healthcare related field.
Experience in the coordination of intergroup or multi‑site clinical studies.
CCRP or CCRC certification.
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Project Management and Information Technology
Industries Hospitals and Health Care
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