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Senior Scientist


This is a Full-time position in Plymouth, MN posted April 7, 2021.

Job Title: Senior Clinical Research Specialist
Location: Plymouth Minnesota
Duration: 9-12+ months (possibility of extension)

Primary Duties and Responsibilities
? Comply with applicable Corporate and Divisional Policies and procedures.
? Support the development of clinical strategy and study design.
? Write study protocols, study reports, and scientific papers for publication by evaluating scientific literature, analyzing scientific data and staying abreast of current clinical practice.
? Support regulatory submissions
? Facilitate communication between Sales and Marketing, R&D, Program Management, Reimbursement, Medical Affairs, Risk Management, Quality and Regulatory Affairs, and investigational sites.
? Oversee study Steering Committees and Publication Committees, consisting of physician Key Opinion Leaders globally.
? Present clinical study results at investigator meetings
? Participate in and support audits.
? Participate in root cause analysis, preventive or corrective actions, and effectiveness monitoring.
Required Qualifications:
? Bachelor’s degree in engineering, medicine, healthcare or sciences
? 5+ years of clinical research work experience
? Demonstrated understanding of business environment and relates extensive knowledge of internal and external technological activities to trends.
? Ability to participate in the development of other technical contributors by facilitating training and providing feedback and guidance.
? Ability to plan and organize project assignments of substantial variety and complexity.
? Requires ability to be innovative, resourceful, and work with minimal direction
? Requires excellent organization, problem solving, and communication skills and the ability to
work effectively with cross-functional teams

? Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
? Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
? Strong organizational and follow-up skills, as well as attention to detail.
? Advanced degree in the sciences, medicine, or similar discipline highly preferred
? Experience in the medical device industry
? Experience with international medical device regulations and submissions.
? Familiarity with relevant international regulatory requirements for medical devices including
Quality Systems standards and clinical investigations.



Disha Kakkad

Talent Acquisition Specialist

Experis CORE

Desk # – 414-203-8334 Extn: 7124

100 Manpower Place, Milwaukee WI 53212

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