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  • ID
    #31996566
  • Salary
    TBD
  • Source
    Actalent
  • Date
    2022-01-18
  • Deadline
    2022-03-19

Vacancy expired!

Job Description:Looking to hire an individual with clinical research experience to act as a consultant CRC to support am ongoing clinical trial. The main job duties for this position will be regulatory filing, creating source documents, data entry (EDC), along with patient recruitment and other research administrative duties. This role requires research experience Duties and ResponsibilitiesRegulatory Filling and Submissions

Consenting

Data Entry/Management

Collection of study data and entering data into EDC (as well as keep EDC up to date)

Creating source documents

Chart review/phone screening

Study administration

Any study efforts deemed necessary by site

Requirements:Clinical Research Experience

Highly independent

Willing to obtain Good Clinical Practices (GCP) certified

Experience in study start up (preferred)

This position is not remote

Recruiter:

Shelby Ciardelli (763) 923-2058 sciardelli@actalentservices.com

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Vacancy expired!

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