Medical Project Coordinator

Integrated Resources Inc.; Raynham (MA); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading staffing firm seeks a candidate for an entry-level position in Clinical Affairs, focusing on the coordination of Clinical Evaluation Reports. This role involves scheduling, vendor management, and ensuring regulatory compliance in alignment with safety guidelines. Ideal for candidates eager to build a career in medical affairs with a premier organization.

Qualifications

• Entry-level position.
• Knowledge of medical device clinical and regulatory requirements preferred.
• Strong verbal and written communication skills.

Responsibilities

• Support Medical Affairs in coordinating Clinical Evaluation Reports.
• Schedule review meetings and manage timelines.
• Ensure compliance with safety and efficacy regulations.

Skills

Communication

Multi-tasking

Organization

Microsoft Office

Medical Writing

Presentation Skills

Education

Broad knowledge of medical device clinical and regulatory requirements

Job description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Job Description and Responsibilities:

This individual will primarily support Medical Affairs in the coordination of Clinical Evaluation Reports (CER) across DePuy Synthes. This may entail scheduling CER review meetings, tracking CER timelines, vendor management, and 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.

• Ensure personal and company compliance with all Federal, State, local, and company regulations, policies, and procedures for health, safety, and environmental compliance.

Job Qualifications

Education

Knowledge/Requirements

• This is an entry-level position.

• Broad knowledge of medical device clinical and regulatory requirements is preferred.

Additional Requirements

• Strong skills and demonstrated competencies in the following areas are required:

o Verbal and written communication skills

o Proven ability to multi-task

o Strong organizational skills

o Proficiency with the Microsoft Office suite

o Medical writing and presentation skills