Clinical Research Specialist

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Clinical Research Specialist

5 months with a possibility to extend

Medtronic – Santa Rosa, CA

Duties:

• Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.
• Assist in preparation of study materials and/or training.
• Interface with, and assure training of investigators, site staff, and Medtronic clinical staff.
• Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).
• May arrange conference calls, staff meetings and training events.
• Assist data management group with review of clinical data/information and oversight of data correction.
• May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).
• Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.
• Contribute to ongoing SOP development and review.
• Participate in training to enhance knowledge base.
• Must be willing to assist with other duties as needed such as filing and document tracking.
• Must have ability to prioritize and critical thinking skills and previous clinical research experience.
• Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy.

• Previous clinical research experience
• Ability to prioritize and strong critical thinking skills
• Attention to detail and strong communication skills

All your information will be kept confidential according to EEO guidelines.

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