Clinical Trials Research Associate II (Durational with Full Benefits) in Los Angeles

Full-time @Kaiser Permanente in Healthcare
  • Los Angeles, California View on Map
  • Apply Before : September 30, 2022

Job Description

Join healthcare leader Kaiser Permanente as Clinical Trials Research Associate II (Durational with Full Benefits) in Los Angeles. Read role and responsibility to apply Kaiser Permanente is careers in Los Angeles California.

 

Position : Clinical Trials Research Associate II (Durational with Full Benefits)

Location :  Los Angeles, California

Job Type : Full-time

Job details:

Description:

Coordinates day-to-day activities of several small scale project(s) or phases of one or more larger projects. May oversee assigned work of project staff. Works under general supervision. Final review required for each phase of project.

Essential Responsibilities:

Coordinates day-to-day activities of several small scale project(s) or phases of one or more larger projects. Collects project data through interviews, chart review or other methods. May collect, secure and assist with biospecimen management.
May assist in development of study tools (e.g. tracking forms, questionnaires, chart review forms, etc.).
Assists with and/ or oversees assigned study activities (e.g. data collection and validation, recruitment activities, pilot studies, focus groups, etc).
Drafts project progress reports collaboratively.
May participate in the training of new team members and/or clinical staff. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites.
Adheres to compliance and privacy/ confidentiality requirements and standards. Adheres to GCP and compliance regulations for clinical trials.
Assists with and/ or oversees quality assurance of study activities; ensures quality data.
Acquires and maintains knowledge of KP systems and databases.
Identifies, recommends and implements solutions to study issues.
May interface with IRB and/ or draft portions of IRB protocols, amendments, continuing reviews, etc.
May supervise the day-to-day activities of project staff (ex. assign work and evaluate performance, etc).
May assist with staff hiring and training.
May contribute to portions of study presentations.
Serves as a member on department or study-related committees.
May track expenses and monitor budget. May recommend budget actions/ decisions.
May provide information and oversight for invoices.
Reviews scientific literature and synthesizes and summarizes information.

Basic Qualifications:

Experience

Minimum two (2) years of experience in public health, healthcare administration, epidemiology, or healthcare-related field.
Minimum one (1) year of experience coordinating research projects under specific guidance.
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; OR
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR
Minimum one (1) year experience in handling, processing, and preparing biospecimens for laboratory analysis and/or transport.

Education

Bachelor’s degree in public health, healthcare administration, epidemiology, or health-related field (ex. Biology, Psychology, etc.), OR four (4) years of experience in a directly related field.
High School Diploma or General Education Development (GED) required.

License, Certification, Registration

N/A

Additional Requirements:

Experience with interviewing (by phone and/or in-person) and medical chart review.
Experience in quantitative and/or qualitative data interpretation.
Experience coordinating one or more projects OR
Experience with biospecimen handling, collection, and processing
Experience with Clinical lab activities
Professional oral and written communication skills.
Must be able to work in a Labor/Management Partnership environment.

Preferred Qualifications:

Master’s degree in public health, healthcare administration, epidemiology or related field.
Preferred Vaccine Clinical Trials-related experience.

 

Other Details

Primary Location: California,Los Angeles,1505 N. Edgemont Medical Offices

Scheduled Weekly Hours: 40

Shift: Day
Workdays: Mon – Fri
Working Hours Start: 08:00 AM

Working Hours End: 05:00 PM

Job Schedule: Full-time

Job Type: Standard

Employee Status: Regular

Employee Group/Union Affiliation: NUE-SCAL-01|NUE|Non Union Employee

Job Level: Individual Contributor

Department: Research and Evaluation, Clinical Trials

Travel: Yes, 20 % of the Time

Kaiser Permanente is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.

 

Career Tag :  Kaiser Permanente Jobs in Los Angeles, Kaiser Permanente career in Los Angeles, Kaiser health jobs in Los Angeles, Healthcare jobs in Los Angeles California, Jobs in Los Angeles California, Los Angeles jobs, Hiring nearby in Los Angeles California

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