Clinical Research Associate I
Idexcel3
Posted: December 5, 2016
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Quick Summary
Clinical Research Associate I is responsible for conducting clinical trials and managing data for pharmaceutical and biotechnology companies.
Required Skills
Job Description
About IDEXCEL, INC
Idexcel is a global staffing and IT services organization, with a mission to bring great people and great organizations together. Our diverse client base represents a wide range of industries, including technology, telecom, insurance, healthcare, manufacturing, banking & financial services, food & commodities trading and federal organizations. Our teams of experienced recruiters directly work with client companies seeking exceptional people to help with their business initiatives.
Idexcel, Inc. is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, disability, military status, national origin or any other characteristic protected under federal, state, or applicable local law.
Clinical Research Associate I
12/19/2016 to 04/28/2017
Marlborough, MA, USA, 01752
$29.72/HR on w2
BACHELORS DEGREE REQUIRED. MUST HAVE RELEVANT 2 YEARS WORK EXPERIENCE OF CLINICAL RESEARCH..
Will be assisting physicians trying to enroll in program for diagnosis of ALZHEIMERS.
Will be working with customers, must have professional demeanor, excellent communication skills.
JOB TITLE: CLINICAL RESEARCH COORDINATOR LOCATION: Massachusetts - Marlborough Clinical Research Coordinator Location: Massachusetts - Marlborough Clinical Research Coordinator wanted for clinical study
Job function includes, study coordination and implementation of a new clinical study.
The position arranges and coordinates clinical study start up activities and plays a key role in assisting the Clinical Operations team in recruiting sites.
The position works closely with the Site Principal Investigators, Clinical site personnel, members of the GEHC team, as well as with the Study Sponsors, and the institution, to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of clinical studies.
It is a full time position, Monday-Friday. Ability to travel within then US up to 20%, as needed.
Positive candidate must possess the following: • Experience as a study coordinator or research assistant for 1-2 years in a hospital/outpatient setting, or within a CRO • High organizational ability with strong attention to detail • Flexibility with a team player attitude • Professionalism • Proficient with Microsoft Office, Outlook and Internet Explorer • Critical thinker and problem solver
Education Requirements: 4 yr Bachelor’s Degree. Clinical research experience required.
Sandra Taylor
571-267-4186
Sandra Taylor
571-267-4186