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Clinical Research Coordinator
4 months ago
Description: PART TIME, 20 HOURS PER WEEK
Job Summary -
The Research Coordinator will assist an Investigator, Research Associate or Project Manager with operationalizing the tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results.
This is a part time role- 20 Hours per Week
Major Responsibilities/Essential Functions * (In order of importance, list primary job duties this position is responsible for achieving.
* Recruits and consents research participants.
* Conducts telephone or in-person interviews with participants including screening for eligibility.
* Performs follow-up (by telephone, e-mail and/or mail) with study participants.
* Prepares, mails and processes questionnaires and other study correspondence.
* Assist in tracking study participants using MS Excel.
* Keeps accurate and detailed records and files of work.
* Reviews, edits, cleans and enters participant data into a database.
* May assist with literature reviews for proposal submissions and manuscript preparation.
* Bookkeeping related to study budgets (ordering supplies, requesting checks for payment & participant incentives)
* Miscellaneous administrative tasks (typing labels, copying, faxing, meeting preparation, note-taking, transcribing audio files, etc.)
Additional Skills & Qualifications
Qualifications *
Minimum Education (Indicate minimum education or degree required.)
* Bachelors degree in science, social science, allied health science, public health or medical field OR four (4) years of experience in a directly related field.
* High school diploma or General Education Development (GED) required.
Preferred Education (Indicate preferred education or degree required.)
* Bachelors degree in science, social science, allied health science, public health or medical field.
Skills:
Chart review, Patient recruitment, Edc, Emr, Clinical research, Gcp
Top Skills Details:
Chart review,Patient recruitment,Edc,Emr,Clinical research,Gcp
Additional Skills & Qualifications:
minimum requirements:
* BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
* Minimum 3 years in Clinical Research and preference for relevant healthcare experience
* Certification of CCRC or CCRP preferred
* Experience of EDC entry and query resolution preferred
About Actalent
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Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
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