Senior Clinical Research Coordinator at Providence
Portland, OR 97225, USA -
Full Time


Start Date

Immediate

Expiry Date

27 Jul, 25

Salary

0.0

Posted On

27 Apr, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Clinical Research Associates, Study Reports, Medical Terminology

Industry

Hospital/Health Care

Description

DESCRIPTION

The Senior Research Coordinator will function under the supervision of the Clinical Research Manager. Responsible for the coordination of study activities, the collection and delivery of study data, and the communication between investigators, study team, and sponsor; interact closely with investigators, sponsors, monitors, regulatory/budget/contract Clinical Research Associates (CRAs), and Institutional Review Board (IRB) to establish research plans and project timetables and coordinate resources needed to ensure productivity and timely completion of project; assist with the implementation of Quality Assurance (QA) tools and the conduct of QA audits as needed to ensure the adherence of study protocol and the compliance of clinical trials to applicable regulations; provide research development support for investigator initiated trials (IITs); serve as a study monitor on IITs; assist with development and implementation of departmental Standard Operating Procedures (SOPs); assist with training and mentoring new staff.
Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence St Vincent 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 Science or Health-related field.
  • Upon hire: Association of Clinical Research Professionals (ACRP), Society of Clinical Research Associates (SOCRA) certificate, or equivalent
  • 5 years Experience as Clinical Research professional supporting all aspects of clinical research with at least 3 years in neurosciences.
  • Experience using medical terminology
  • Experience in designing case report forms, developing study reports, and auditing study data.
  • Experience in training and mentoring research staff.
  • Experienced in the development and implementation of policies and standard operating procedures.
Responsibilities

Please refer the Job description for details

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