Project Coordinator
Hello,
My name is Donald and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Project Coordinator for a prominent client of ours. This position is located in Raynham, MA. Details for the positions are as follows:
Job Description:
This individual will primarily support Medical Affairs in the coordination of Clinical Evaluation Reports (CER) for our Client.
This may entail scheduling CER Review meetings, tracking CER timelines, vendor management, and tracking literature search requests to ensure CER timelines are met.
Business Leadership
Ensure that safety and efficacy of our products are documented, processed, and reported following Company guidelines, internal business practices, and regulatory guidance to ensure compliance with worldwide safety regulations and corporate policies.
Administrative Leadership
Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance.
Education
BS in Life Sciences, PMP preferred
Knowledge/Requirements
Broad knowledge of medical device clinical and regulatory requirements is preferred.
This is an entry level position
Additional Requirements
Strong skills and demonstrated competencies in the following areas are required:
Verbal and written communication skills
Proven ability to multi-task
Effective time management skills
Strong organizational skills
Proficiency with the Microsoft Office suite
Medical writing and presentation skills
If you are interested in hearing more about the position please respond to this posting with your resume attached.
Regards,
DonaldEstimated Salary: $20 to $28 per hour based on qualifications.
My name is Donald and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Project Coordinator for a prominent client of ours. This position is located in Raynham, MA. Details for the positions are as follows:
Job Description:
This individual will primarily support Medical Affairs in the coordination of Clinical Evaluation Reports (CER) for our Client.
This may entail scheduling CER Review meetings, tracking CER timelines, vendor management, and tracking literature search requests to ensure CER timelines are met.
Business Leadership
Ensure that safety and efficacy of our products are documented, processed, and reported following Company guidelines, internal business practices, and regulatory guidance to ensure compliance with worldwide safety regulations and corporate policies.
Administrative Leadership
Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance.
Education
BS in Life Sciences, PMP preferred
Knowledge/Requirements
Broad knowledge of medical device clinical and regulatory requirements is preferred.
This is an entry level position
Additional Requirements
Strong skills and demonstrated competencies in the following areas are required:
Verbal and written communication skills
Proven ability to multi-task
Effective time management skills
Strong organizational skills
Proficiency with the Microsoft Office suite
Medical writing and presentation skills
If you are interested in hearing more about the position please respond to this posting with your resume attached.
Regards,
DonaldEstimated Salary: $20 to $28 per hour based on qualifications.
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