Clinical Research Associate II (CRA II)
Kelly Services - Jacksonville, FL

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Clinical Research Associate
Every day, Kelly Scientific Resources (KSR) connects clinical research professionals with opportunities to advance their careers.
We currently have a contract opportunity for a Clinical Research Associate (CRA) in Jacksonville, FL .

Job Responsibilities (other duties may be assigned):
Education and experience required
Bachelors degree or equivalent relevant experience.
Six years of working experience in clinical research setting with a minimum of four years as a clinical research monitor.
Working knowledge of regulations and standards applied in clinical area and medical devices.
Strong knowledge, understanding and application of principles, concepts and practices of clinical investigations/studies.
Strong organizational, analytical, oral and written communication skills.
Technical writing skills.
Knowledge of the application of requirements to new products and processes.
Ability to collect and analyze data.
Ability to develop innovative solutions to problems with minimal complexity.
For immediate consideration
Kelly Scientific Resources has?grown into a $270 million global business as the scientific business unit of Kelly Services. Our recruiting consultants place clinical, regulatory and medical affairs, data management and biostatistics professionals to the pharmaceutical, biotechnology, medical device, CRO and university research communities. We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide: , click the Apply Now! button, or refer a friend by clicking the E-mail this job link provided. :
Under general supervision, plan and monitor human clinical trials in compliance with internal standard operating procedures, Good Clinical Practices (GCP) and applicable Regulations and Guidelines.
Coordinate protocol, informed consent and case report form development and compilation.
Insure appropriate trial agreements are signed and materials are distributed.
Complete source document verification, query generation and acceptance, and test article accountability both remote and on-site.
Monitor and secure protocol and regulation compliance at investigational sites.
Review, retrieve, and report the trial data as the requirements dictate or as appropriate.
Adhere to environmental policy and procedures and supports department environmental objectives.
Identify potential clinical sites, qualify clinical sites, monitor clinical studies per GCP, maintain study-related documents. Up to 50% travel to clinical sites and clinical research organizations.
Plan and develop study request for proposals, site training documentation, protocols, informed consent forms, CRFs, and other study materials.
Prepare and present clinical studies at site initiation or investigator meetings and report study results.
Perform other relative duties as assigned by management. .
Kelly Services is an Equal Opportunity Employer.

About Kelly Services ®

Kelly Services, Inc. (NASDAQ: KELYA, KELYB) is a leader in providing workforce solutions.
Kelly ® offers a comprehensive array of outsourcing and consulting services as well as world-class
staffing on a temporary, temporary-to-hire, and direct-hire basis.
Serving clients around the globe, Kelly provides employment to more than 560,000 employees annually.
Revenue in 2012 was $5.5 billion.
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