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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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