Clinical Research Coordinator

Pacific Neuropsychiatric Specialists

Job Location:

Orange, CA - USA

Hourly Salary: $ 25 - 35

Posted on: 8 hours ago

Vacancies: 1 Vacancy

Job Summary

Benefits:

401(k) matching
Dental insurance
Health insurance
Paid time off
Training & development
Vision insurance

PNS Clinical Research (PNSCR) is the research division of Pacific Neuropsychiatric Specialists a private practice spanning 6 locations and 40 providers. PNSCR conducts phase II-IV psychiatry trials for indications including MDD Schizophrenia Alzheimers Disease and bipolar disorder.

Job Summary:

Under policy direction from the Clinical Research Director the Clinical Research Coordinator will play a crucial role in supporting clinical research activities ensuring adherence to protocols and contributing to the advancement of medical knowledge. The Clinical Research Coordinator is responsible for assisting in patient identification recruitment and enrollment strategies and performing other clinical research duties for the office. The Clinical Research Coordinator is responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization) GCP (Good Clinical Practices) protocol and company guidelines regulations and policies.

Key Responsibilities:

Assist PI physicians and clinical staff in patient identification recruitment and enrollment strategies.
Ensure patient enrollment and research activities comply with established protocols regulatory and monitoring agency standards and sponsor guidelines.
Screen potential patients for protocol eligibility.
Present trial concepts and details to patients take part in the informed consent process and enroll/randomize patients into the study.
Conduct clinical trial visits including screening and follow-up and track participant data per protocol requirements.
Complete accurate and concise documentation of all participant records and other source documentation and forms per protocol.
Accurately document study data in Case Report Forms (CRFs) and electronic databases resolving any data queries from sponsors in a timely manner.
Review patient charts for changes in condition adverse events concomitant medication use protocol compliance and response to study drug and thoroughly document all findings.
Manages the storage dispensation and tracking of investigational products as per protocol.
Attend Site Initiation Visits facilitate routine monitoring visits conduct Close Out Visits and proactively work to resolve site action items in collaboration with trial monitors. Perform basic lab duties including processing of samples centrifuging storing and shipping of study specimens.
Schedule patient screening appointments treatments and laboratory assessments required by the protocol.
Prepare study data for progress reports analysis and meeting presentations.
Participate in required clinical research education and training programs.
Attend and represent the site at study-related investigator conferences
Effectively communicate and collaborate with w/ study team including internal and external parties sponsors PI and study participants.
Show initiative to identify and implement ways to improve job workflow and surroundings.
Plan work in a manner that allows timely completion of all assignments and tasks.

Required Qualifications:

Bachelors Degree in a health-related discipline (i.e. pharmacology nursing biology etc.) or equivalent experience.
1-3 years of clinical research experience.
Current CPR/Basic Life Support (BLS) certification (upon hire)
Current Good Clinical Practice (GCP) Certification (upon hire)
Detail-oriented and meticulous in all aspects of work.
Ability to prioritize tasks effectively manage time and allocate resources efficiently to meet tight study deadlines.
Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative

Preferred Qualifications:

Prior clinical research experience with neurological indications such as Alzheimers and Tardive Dyskinesia
Prior clinical research experience with psychological indications such as Major Depressive Disorder Bipolar Disorder Schizophrenia and PTSD

Compensation & Benefits:

PNS offers a competitive compensation package including; medical dental vision and paid time off for full-time employees.
Hourly rate is based on skill experience and tenure of profession.

This job description is intended to outline the general responsibilities and qualifications for the Clinical Research Coordinator role. Duties and responsibilities may evolve and the Clinical Research Coordinator may be required to perform other tasks as assigned.

Compensation: $25.00 - $35.00 per hour

We are Pacific Neuropsychiatric Specialists (PNS) and our experience enables us to offer effective outpatient individualized psychiatry care. Our psychiatry team provides psychiatric treatments for children adolescents adults and seniors from multiple offices located throughout Orange County we do accept patients from the entire United States as well. Our psychiatrists treat a number of mental health disorders including anxiety stress PTSD bipolar schizophrenia dementia depression ADD ADHD alcohol and chemical dependency and more. Our Psychiatry practice was founded on the principles of treating patients with care compassion and understanding.

Required Experience:

Benefits:401(k) matchingDental insuranceHealth insurancePaid time offTraining & developmentVision insurancePNS Clinical Research (PNSCR) is the research division of Pacific Neuropsychiatric Specialists a private practice spanning 6 locations and 40 providers. PNSCR conducts phase II-IV psychiatry tr...