Lead Clinical Research Coordinator at Providence Medical Grp.

Mission Viejo, California, United States -

Full Time

Start Date

Immediate

Expiry Date

16 May, 26

Salary

61.24

Posted On

15 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Portfolio Management, Pre-study Communication Coordination, Staff Training, Patient Screening, Eligibility Confirmation, Registration, Data Quality Control, Study Evaluation, Direct Patient Care, Investigator Interaction, Sponsor Interaction, Research Committee Collaboration, Confidentiality, Attendance, Punctuality, Microsoft Office

Industry

Hospitals and Health Care

Description

The Lead Research Coordinator will function under the supervision of the Nurse Manager, coordinating and maintaining diverse activities related to clinical research studies. This includes but is not limited to clinical trial portfolio management, pre-study communication coordination, new staff training, patient screening, confirming eligibility, registration, quality control of data compilation and submission, study evaluation, as well as direct patient care. Interacts closely with institutional investigators and industry sponsors. Collaborates with the Research Committee throughout study through completion for treatment and complex trials. Must uphold the standards of confidentiality, attendance and punctuality. Performs all duties in a manner which promotes team concept and reflects the sisters of Providence mission and philosophy. Providence caregivers are not simply valued – they’re invaluable. Join our team at Mission Hospital Regional Medical Center and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them. Required Qualifications: Bachelor's Degree in Scientific or Health Services discipline 3 years of Clinical research experience in a healthcare with 1 year (in house) experience in Oncology clincial trials. 3 years of Microsoft Office experience. 1 year of experience with medical terminology. 1 year of experience in electronic data capture systems and electronic medical records systems. Preferred Qualifications: Master's Degree ACRP/SOCRA certification or other clinical research certification upon hire Why Join Providence? Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities. At Providence, our strength lies in Our Promise of “Know me, care for me, ease my way.” Working at our family of organizations means that regardless of your role, we’ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable. Posted are the minimum and the maximum wage rates on the wage range for this position. The successful candidate's placement on the wage range for this position will be determined based upon relevant job experience and other applicable factors. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits. Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. The Sisters of Providence and Sisters of St. Joseph of Orange have deep roots in California, bringing health care and education to communities from the redwood forests to the beach shores of Orange county - and everywhere in between. In Southern California, Providence provides care throughout Los Angeles County, Orange County, High Desert and beyond. Our award-winning and comprehensive medical centers are known for outstanding programs in cancer, cardiology, neurosciences, orthopedics, women's services, emergency and trauma care, pediatrics and neonatal intensive care. Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School. Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.

Responsibilities

The Lead Research Coordinator manages diverse clinical research activities under the Nurse Manager, including trial portfolio management, staff training, patient screening, data quality control, and direct patient care. This role involves close interaction with institutional investigators, industry sponsors, and the Research Committee throughout the study lifecycle.