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Clinical Research Associate

Santa Monica, CA 90401

Posted: 12/06/2022 Job Number: z5G7h3l6a1kMvyS65NP3c6SA-7PMR8WwL6T-KyzRXEw= Pay Rate: 50-51 Hourly USD

Job Description

Job Title: - Clinical Research Associate

Job Location: - 1919 Santa Monica Blvd. Suite 400 Santa Monica, CA 90404

Job Duration: 9+ months (Possibility of extension)

Pay Rate: $51/Hr. on W2

Shift: Day 5x8-Hour (08:00 - 16:30)

If you are interested, Reply to me Yes! I CONFIRM with a copy of your resume in word/pdf format.

Job Description:


The Clinical Research Associate II will assist the research department with case report form (CRF) completion for all clinical research protocols sponsored by various pharmaceutical and biotech companies.

  • 2 years of experience in the field of clinical research
  • Bachelor’s degree required, preferably in biology or science-related field
  • 1 year of experience in a medical office is preferred
  • Must have strong understanding of Good Clinical Practice in Clinical Trials, scientific principals, and clinical trial design
  • Experience interacting with patients and/or families, pharmaceutical company representatives and other project personnel.
  • Must demonstrate excellent communications skills, both written and verbal
  • Ability to multi-task and manage time efficiently
  • Ability to respond to common inquiries or complaints from patients, team members, pharmacy sponsors, or regulatory agencies.
  • Able to work carefully and efficiently under stressful and or high demand situations
  • Strong knowledge of GCP and ICH guidelines & local regulatory requirements
  • Proficiency with EDC, CTMS and eTMF systems
  • ACRP or SOCRA certification a plus, not required
  • Candidates MUST be LOCAL to the job; no more than one hour commute away, preferably 1/2 hour commute.

  • Reports and communicates to the sponsor/CRA/monitor/IRB.
  • Coordinate data for completion of case report forms (CRFs), either paper or electronic data capture and perform data entry for clinical research trials and projects.
  • Review all clinical study records to ensure complete documentation in compliance with regulations.
  • Prepares charts for monitoring visits.
  • Answers sponsor queries in a timely manner.
  • Obtain physician signatures on CRFs and other study documentation as needed.
  • Assists the research staff in meeting all data lock and query resolution deadlines.
  • Updates outside sponsors as needed on query resolution, outstanding number of CRFs to be completed, etc.
  • Provide support (including administrative/clerical) to staff and external sources related to current research projects.
  • Attend meetings and telephone conferences related to research activities as needed.
  • Act as liaison between research department and sponsor as needed to ensure timely CRF completion.
  • Generate clinical SOPs, policies, charters, and plans according to US and international guidelines as applicable.
  • Maintain research charts and subject records while prioritizing and maintaining progress on multiple scientific projects.
  • Obtain medical records, death certificates and death information for all subjects as needed.
  • Interact appropriately with other members of the clinical team and office personnel
  • Advise supervisor, physicians, administrator of potential or actual problems; ie, report serious adverse events.
  • May participate in CRF development for Investigator Initiated Trials
  • May be involved in training and education of other CRAs.
  • Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested.
  • Review and adhere to department policies and procedures to maintain proficiency in operating guidelines.
  • Maintain confidentiality when performing all duties and responsibilities.
  • Demonstrate willingness to assist co-workers in completion of daily tasks or special projects to support the department’s efficiency.
  • Will support finding creative solutions to complex scientific and business challenges.
  • Maintain appropriate records, notification of time worked, vacations, seminars, and professional time commitments related to this position.
  • Must show high energy with a focus in meeting deadlines
  • Expected to focus on providing cutting edge technology that solves real business challenges and ultimately produces better treatment alternatives for patients.
  • Expected to maintain customer focus in a way that ensures desired outcomes are achieved;
  • Perform other duties as assigned
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