
Job Information
Randstad Part Time Clinical Trials Assistant, Global Medical Affairs in North Billerica, Massachusetts
Part Time Clinical Trials Assistant, Global Medical Affairs
job details:
location:North Billerica, MA
salary:$30 - $35 per hour
date posted:Thursday, February 18, 2021
experience:Experienced
job type:Temporary
reference:S_877275
questions:leslie.thompkins@randstadusa.com978-671-8450
job description
Part Time Clinical Trials Assistant, Global Medical Affairs
6-10 Hours per week
Assist the Investigational Sponsored Trials Program (IST) Team by providing administration and project tracking support.
Responsibilities:
Assist the IST Team with trial progress tracking by updating the IST Tracking System.
? Open to learning and becoming well versed in working with the IST dedicated Tracking System.
? Support the IST Team with ongoing management of Investigational Sponsored Research.
? Process Research Data Collection Forms i.e. Progress Reports, Agreements, Product Shipment and Inventory Documents, including tracking, and quality control as appropriate.
? Provide general administrative support to the IST Team and Program Director.
? Assist project teams with study specific documentation as appropriate.
? Assist in the set up, organize and maintain research documentation.
? Assist in co-ordination of Investigator payments, if applicable.
Working hours: 9:00 AM - 12:00 PM
Skills:
Bachelor degree or equivalent in a scientific or health related field required.
Overall combination of 3 years administrative support experience scientific and/or clinical experience in industry
Equivalent combination of education, training and experience.
Computer skills including working knowledge of Microsoft Word, Excel, Powerpoint, and Outlook.
** Effective time management and Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
Written and verbal communication skills including good command of English language.
Ability to establish and maintain effective working relationships with coworkers, and manager.
Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Education:
Bachelors
Experience:
Experienced
Qualifications:
Knowledge/training in Prostate Cancer, Cardiovascular disease and drugs, and imaging agents an advantage.
Research or health care related academic or work experience preferable.
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