Internship Program: Clinical Operations

 

Position Summary: To fulfill the responsibilities assigned to gain knowledge of both Clinical Operations and Clinical Development.

Responsibilities:

  • Support the Clinical Operations/Development Team members with the tasks associated with implementation and conduct of clinical studies

  • Assist the Clinical Operations/Development team in planning maintaining and closing multiple clinical studies at different phases

  • Maintain trial master file, study site records and files and ensure compliance with applicable SOPs Create, implement, and maintain systems to track study metrics

  • Coordinate meetings including the generation of agendas, minutes and decision/action logs

  • Process study-related documents and materials – to include collation, filing, routing coordination of third-party provider document shipments

  • Assist team members with overall study management

  • Process vendor invoices and assist in tracking spending against approved budget. Track approvals and completion of required documents

  • Perform other functions as necessary or as assigned

Required Education, Qualifications and Experience:

  • Undergraduate student entering Junior or Senior year of study in a science-related field (Biological sciences preferred)

  • Capability to conceive and execute original research projects

  • Demonstrated leadership and initiative

  • Excellent written, oral, and presentation skills

  • Proficient in MS office software

  • Extremely detail-oriented

  • Ability to work onsite in Germantown, MD

  • Good interpersonal skills and ability to work in a team environment contributing to a collaborative work atmosphere.

  • Must meet the following eligibility criteria:

    • Legal authorization to work in the U.S. (must present documents)

    • Enrollment in a full-time undergraduate or graduate program, returning to the academic program following internship

To submit your CV for our consideration, please email us at jobs@amarexcro.com.

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