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Clinical Research Associate (CRA)

Alpha Consulting Corporation

Location:
Wilmington, DE
Posted Date:
5/20/2014
Position Type:
Contract
Job Code:
14-00484
Salary:
Required Education:
High school or equivalent
Areas of Expertise Desired:
Pharmaceutical,

Job Description

CLINICAL RESEARCH ASSOCIATE (CRA)

REQUIREMENT #14-00484
RECRUITER:  CHERYL AMBROSE
JOB LOCATION: WILMINGTON, DE
MAY 20, 2014

*** CANDIDATES MUST WORK ON OUR W-2 ONLY ***

Project Description:  Primarily responsible for site management within a clinical study. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Able to solve complex problems within a range of studies.

The CRA works in close collaboration with other CRAs, site monitoring partners and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner.

The CRA is responsible for site management according to the client’s Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations and deliver according to the commitment in the individual trials.

Responsibilities:
•   Obtain and maintain essential documentation in compliance with ICH-GCP, the client’s Procedural Documents and local regulations both in the office and at site.
•   Actively participate in local Study Delivery Team meetings
•   Contribute to the selection of potential investigators
•   Train, support, and advise Investigators and site staff in study related matters
•   Contribute to national Investigators meetings
•   Drive performance at the sites
•   Proactively identify study-related issues and escalates as appropriate
•   Update IMPACT and other systems with data from centres as per required timelines
•   Ensure compliance with the client’s Code of Conduct and company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).

Required Skills: Experience in Clinical Site Management, 10% travel required.



This 12 month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Cheryl: cambrose@alphaconsulting.com

Requirements

•   Obtain and maintain essential documentation in compliance with ICH-GCP, the client’s Procedural Documents and local regulations both in the office and at site.
•   Actively participate in local Study Delivery Team meetings
•   Contribute to the selection of potential investigators
•   Train, support, and advise Investigators and site staff in study related matters
•   Contribute to national Investigators meetings
•   Drive performance at the sites
•   Proactively identify study-related issues and escalates as appropriate
•   Update IMPACT and other systems with data from centres as per required timelines
•   Ensure compliance with the client’s Code of Conduct and company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).

Required Skills: Experience in Clinical Site Management, 10% travel required.

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