1 Principal Investigator Job in Redmond, WA

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Principal Investigator

Eastside Research Associates

Redmond, WA | Full Time

$84k-127k (estimate)

3 Weeks Ago

Principal Investigator

$84k-127k (estimate)

Full Time 3 Weeks Ago

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Eastside Research Associates is Hiring a Principal Investigator Near Redmond, WA

Eastside Research Associates (ERA) is a fast-growing clinical research company that is seeking a Clinical Recruitment Coordinator to facilitate participant recruitment and enrollment in a variety of ongoing clinical trials. They will support ERA in achieving required patient enrollment targets by recruiting participants via outreach, phone calls, emails, social media, and networking. They will coordinate participant visits and manage participant scheduling in our outpatient clinics. Must be a self-starter with strong communication skills, high organizational ability, and strong attention to detail.

Description

SUMMARY

The Principal Investigator (PI) oversees all research projects and has overall accountability for the study. Following Good Clinical Practice (GCP) guidelines, the position will ensure that investigations are conducted according to the signed investigator statement, investigational plan, applicable regulations; for protecting the rights, safety, and welfare of subjects, and for the control of the investigational product under investigation. This position collaborates closely with Research Coordinators and Sub Investigators.

ESSENTIAL DUTIES

Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes.

Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP/ regulatory compliance.

Evaluates and assesses participants to ensure only eligible participants enroll into the trials.

Report to the sponsor adverse experiences that occur in the course of the investigation. Will read and understand the information in the IB, including the potential risks and side effects of the drug.

Participates and engages in successful delivery and retention of study participants.

Interacts positively and collaboratively with sponsors, clients and team members.

Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.

Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.

Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

COMPETENCIES

Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
Must possess a high degree of urgency, self-motivation, integrity and dependability.
Ability to provide outstanding patient care
Ability to build rapport with patients and sponsors
Ability to work independently to identify problems and implement solutions
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

WORK ENVIRONMENT

Clinical office environment
May involve some exposure to hazards or physical risks, which require following basic safety precautions.

PHYSICAL DEMANDS

Frequent use of keyboard and mouse
Frequent use of computer monitors and other electronic screens
Frequent standing, walking, bending, and stooping
Occasional ability to lift 10 pounds

EDUCATION & EXPERIENCE:

REQUIRED

Minimum 3 years of experience in Clinical Trials Research or 10 years post training experience as a physician in general medicine or internal medicine
Clinical skills including phlebotomy, vitals, ECGs/EKGs, IVs, etc.
Knowledge of clinical research operations, including Good Clinical Practice guidelines
Current Healthcare Provider BLS certification
Excellent written and verbal communication Skills
Experience with Microsoft Office
High attention to detail
Strong organizational and time management skills

PREFERRED

Principal Investigator Experience

TRAVEL

Between 5% - 10% domestic travel

OTHER DUTIES

In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.

Eastside Research Associates provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on Eastside Research Associates. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.

Salary

$122 - $169 per hour

Job Summary

JOB TYPE

Full Time

SALARY

$84k-127k (estimate)

POST DATE

04/15/2024

EXPIRATION DATE

06/13/2024

RN – Clinical Research Patient Recruitment Specialist

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The following is the career advancement route for Principal Investigator positions, which can be used as a reference in future career path planning. As a Principal Investigator, it can be promoted into senior positions as a Compliance Specialist IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Principal Investigator. You can explore the career advancement for a Principal Investigator below and select your interested title to get hiring information.