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Randstad Clinical Trial Associate in Cambridge, Massachusetts

Clinical Trial Associate

job details:

  • location:Cambridge, MA

  • salary:$23.34 - $27.46 per hour

  • date posted:Wednesday, February 24, 2021

  • experience:1 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:35387

job description

Clinical Trial Associate

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Cambridge, Massachusetts

job type: Contract

salary: $23.34 - 27.46 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

  • Maintenance of informational databases and program tracking reports, participate in coordination of clinical trial related activities, authoring of study operations manuals, budgetary oversight and tracking, and providing general program support in a team setting to ensure the successfulexecution of clinical trial tasks and deliverables according to project timelines.

  • Duties may include, but are not limited to, subject tracking, assembly, review, quality control, and tracking of regulatory documents, maintenance and tracking of study materials (including investigational drug), generation and distribution of meeting agendas and minutes in addition to other activities.

  • Effectively and efficiently interact with internal, clinical site and vendor personnel.

  • Have the interest and ability to expand knowledge of clinical trial management procedures and regulatory submission requirements.

  • Learn health care authority regulations and guidelines, and apply to daily activities.

  • Perform day to day activities based on Standard Operating Procedures and Good Clinical Practice (GCP).

  • Learn and execute defined tasks while working closely with others.

  • Assist with in house coordination of activities related to conduct of clinical trials.

  • Demonstrate problem?solving skills, including the identification of problems and proposed solutions, in consultation with more senior team members.

qualifications:

  • Minimum, a BS Degree

  • Highly motivated person with excellent computer skills, who is highly attentive to details, has strong organizational skills, and able to communicate effectively in a fast paced environment

  • Minimum of 1 year work experience in related field

skills: Quality control, SOP, GCP (Good Clinical Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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