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Maple Grove

    Clinical Coordinator - Maple Grove, United States - Collabera

    Collabera
    Collabera Maple Grove, United States

    10 hours ago

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    Description

    Job Description

    Job Description

    Description:

    Working under direct supervision, provide clinical study administrative support to ensure compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards and SJM Standard Operating Procedures. Performs routine assignments in this entry level position. Focus is on supporting administrative functions related to clinical

    study(s) which may include maintaining Clinical Trial Master File, site regulatory documents and device shipping and tracking. Assist with the coordination of safety board meetings which may include preparation of documents, coordination of meeting venue and travel. Provide assistance with core labs which includes tracking receipt of test results and invoices.

    Responsibilities:

    1. File Management

    • Set-up and maintain Clinical Trial Master File.
    • Set-up and maintain site study files.
    • Maintain source document files.

    2. Provide support to Clinical Project Teams

    • Assist with preparation for monitoring visits, such as internal regulatory file reviews and preparation, as appropriate for the assigned study.
    • Maintain records of investigational devices for all assigned regulated studies.
    • Facilitate the order and release of clinical IDE device inventory.
    • Process invoices as needed and review payment report if applicable.
    • Run IRB renewal status report and notify sites of pending IRB renewals.
    • Create site regulatory/subject binder(s) and ship to sites.
    • Assist with collection of site activation documents.
    • Organize and track shipment of study related documents.
    • Support and track shipment of project related equipment/data between centers, sponsor and core labs.
    • Assist with core labs such as tracking receipt of test results and invoices.
    • Attend project related meetings; write meeting minutes as applicable.
    • Assist with Investigator/Committee, etc. meetings such as travel arrangements, hotel, conference rooms, etc.
    • Collect, file and de-identify adverse event source documents.
    • Receive and file study related documents in the appropriate location.
    • 3. Able to handle multiple assignments in a timely manner while meeting assigned deadlines.
    • 4. Communicates and collaborates with all levels of employees, customers, contractors, and vendors.

    Other Duties:

    • Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

    Equipment:

    • Uses standard office equipment, including (but not limited to) personal computer, telephone,
    • FAX, and copier.

    Working Conditions:

    • Normally works in a cubicle situated in open landscape office environment. Air conditioned.
    • Well lighted. Moderate noise level.

    Physical Demands:

    • Primarily sitting. Some walking. Light effort related to moving, lifting and using office supplies and standard office items. Performs tasks which regularly require good correctable vision and hand/eye coordination.

    Qualifications:

    Required:

    • High school diploma/secondary school degree.
    • Proficient in operating a personal computer and in using various PC-based software packages including Word, Excel, or similar word processing/spreadsheet software.
    • Must have strong organizational skills and attentiveness to detail.
    • Must also have verbal and written communication, interpersonal, organizational and basic math skills.
    • The ability to read, write, and communicate effectively in English is also required; this requirement includes clear, understandable speech, demonstrated comprehension skills, and demonstrated competence in English spelling, grammar and punctuation.
    • Must be able to use discretion and handle sensitive/confidential information.
    • The ability to work independently when necessary.
    • The ability to exchange straightforward information, ask questions, and check for understanding.
    • Must be able to maintain regular and predictable attendance.

    Desired:

    • A Bachelor's degree from an accredited university or college.
    • A general familiarity with cardiac, vascular, and/or neuromodulation technologies, and clinical research processes. Previous related experience in a medical device/pharmaceutical company or relevant clinical experience in a clinical/hospital environment.
    • Previous Customer Service experience including interacting with customers, answering customer questions and providing information.
    Company DescriptionCollabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data/AI. With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.

    Company Description

    Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data/AI. With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.
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