Clinical Research Associate (CRA) Jobs

Conshohocken, PA

Job Description

- Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Provide clinical support for projects according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Registry management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP, as applicable.
- Available for travel up to 80% of the time, including overnight stays as necessary.

Education/Qualifications

- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).

In lieu of the above requirement, candidates with two (2) or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered.
- Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements.
- Basic understanding of the clinical trial process.

Experience

Minimum one year (1 year) of clinical research experience to including site monitoring, site management or registry administration.
- Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP.
- General understanding of Serious Adverse Event reporting process.
- Ability to work within a project team.
- Good planning, organization and problem solving abilities.
- Good communication skills, oral and written.
- Good computer skills.
- Works efficiently and effectively in a matrix environment.

Preferred:
- One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical laboratory, research, data analysis, data management or technical writing) is preferred.

For more information please call 888-268-2623

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