Field Based Clinical Research Associate

  • Norristown, PA


: $51,530.00 - $72,960.00 /year *

Employment Type

: Full-Time


: Scientific Research

Field Based Clinical Research Associate

**job details:**

+ location:Norristown, PA

+ salary:$85,000 - $90,000 per year

+ date posted:Monday, August 19, 2019

+ experience:3 Years

+ job type:Permanent

+ industry:Professional, Scientific, and Technical Services

+ reference:29676

**job description**

Field Based Clinical Research Associate

job summary:

**Position: Field Based Clinical Research Associate**

Seeking an experienced CRA, local to the Norristown area, who will assist with administration of clinical research projects, such as: site and investigator recruitment, collecting investigator documentation, site management and site monitoring.

location: Norristown, Pennsylvania

job type: Permanent

salary: $85,000 - 90,000 per year

work hours: 9 to 5

education: Bachelors


+ Assist with Administration of clinical research projects: site and investigator recruitment, collecting investigator documentation, site management, site monitoring, preparing and maintaining proper status reports of activities at investigative sites through the duration of a clinical trial and completing other technical tasks to completion.

+ Qualify, initiate, monitor and close-out clinical investigative sites under supervision from Project Managers, Clinical Regulatory Managers, and Medical Directors.

+ Assist and manage training of new Clinical Research Associates.

+ Provide ongoing assistance and education of investigational sites in principles of Good Clinical Practice (GCP) as it relates to Research involving human and or animal subjects.

+ Ensure subject safety through diligent monitoring of the site's compliance with study protocols and the collection of adverse event information

+ Update, track and maintain study specific trial management tools/system.

+ Monitor Case Report Forms (CRF) for missing implausible data. Assess compliance with investigational product handling procedures. Ensure that all adverse events are collected pursuant to GCP.

+ Report, write narratives and follow-up on reported serious adverse experiences.

+ Assist with generation and reconciliation of queries to investigation sites to resolve problem data.

+ Assist and manage project budget and investigator site budget as needed, attend project team meetings, plan, attend and participate in investigator meetings, and communicate with clients.

+ Generate and track investigational product shipments and storage.

+ Provide coverage to clinical contact telephone lines. Provide answers to common protocol related questions under the supervision of the Project Manager and Medical Director.


+ Bachelor's degree required in the Biological / Health Sciences or a related fields required.

+ Pharmaceutical industry or related experience required.

+ Minimum of 3 years' experience as a Clinical Research Associate required.

+ Ability to travel up to 60%, including overnight.

+ Strong multi-tasking abilities and able successfully handle multiple priorities simultaneously.

+ Proficiency in MS Word, Excel and Outlook.

+ Detail oriented, self-motivated.

skills: CRF, Clinical research, GCP (Good Clinical Practice), Clinical Study Design

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
Associated topics: addiction, behavioral, behavioral healthcare, coordinator, disabilities, npho, outreach, social worker, substance, violence

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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