Regulatory Affairs - Plantation, FL, US

+Job Summary · About Us At Trividia Health we are committed to improving lives through innovative diagnostic solutions As a leader in the medical device and in vitro diagnostics IVD industry we strive for excellence in regulatory compliance quality and customer satisfaction We ar ...

This job involves supporting the regulatory side of the business to ensure compliance with corporate procedures and timely product approvals with domestic and international regulatory requirements. · Assist in the preparation of US, EU, and rest of world regulatory submissions as ...

Advancing Psychiatric & CNS Clinical Research · Next Phase Research is a growing medical research organization specializing in psychiatry and central nervous system (CNS) clinical trials. We are committed to advancing innovative treatments while delivering exceptional patient car ...

We are seeking an experienced Director of Regulatory Affairs to lead our regulatory efforts across global markets. · Lead U.S. regulatory submissions including 510(k)s CLIA waivers and FDA correspondence. · Develop and execute global regulatory strategies for new existing IVD pro ...

· Company Description · Headquartered in the U.S., our client  is a division of a global company devoted to the research and development, manufacturing, and distribution of highly specialized products for Healthcare and Life Sciences worldwide. · This is a great step for someone ...

The Regulatory Affairs Specialist oversees all regulatory matters and executes the strategy to ensure the organization complies with applicable regulations. · ...

The Regulatory Affairs Specialist is responsible for supporting regulatory compliance activities for a well-established medical device organization and ensuring products meet applicable U.S. and international regulatory requirements throughout their lifecycle. · ...

The Regulatory Affairs Specialist is responsible for supporting regulatory compliance activities and ensuring products meet applicable U.S. and international regulatory requirements throughout their lifecycle. · ...

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Department: Regulatory Affairs · Address: 1611 NW 12thAve, Miami, Florida, 33136 · Shift details: Monday- Friday 8:30 am- 5:00pm · **ACHA and CMS experience for this role** · Why Jackson · Jackson Health System is a nationally and internationally recognized academic medical syste ...

Department: Regulatory Affairs · Address: 1611 NW 12thAve, Miami, Florida, 33136 · Shift details: Monday- Friday 8:30 am- 5:00pm · **ACHA and CMS experience for this role** · Why Jackson · Jackson Health System is a nationally and internationally recognized academic medical syste ...

Director of Regulatory Affairs, Regulatory Affairs, Full Time · Department: Regulatory Affairs · Address: 1611 NW 12thAve, Miami, Florida, 33136 · Shift details: Monday- Friday 8:30 am- 5:00pm  · **ACHA and CMS experience for this role** · Why Jackson: · Jackson Health System is ...

This is a contract to hire position for a Regulatory Affairs Specialist responsible for maintaining regulatory compliance. · Maintain regulatory policies and procedures to meet country requirements. · Develop collaborative relationships with functional partners. · ...

We are seeking an enthusiastic hard-working and detail-oriented Regulatory Affairs Specialist responsible for maintaining regulatory compliance. · Direct and coordinate preparation of document packages for regulatory submissions from all areas of the company including internal au ...

We currently have an exciting opportunity available for a Manager, Regulatory Affairs · ...

Remitee is scaling its cross-border payments platform across key markets in LATAM/USA/EU. We are looking for a Head of Regulatory Affairs (Regional) with strong hands-on experience leading regulatory filings, licensing applications, implementation and ongoing maintenance for paym ...

· About Company: · Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience c ...

The Regulatory Affairs Specialist is responsible for clinical research operations duties of a routine and technical nature in support of clinical trials.This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives. ...

The Regulatory Affairs Specialist is responsible for routine clinical research operations duties in support of clinical trials. · ...

We currently have an exciting opportunity available for a · Manager, Regulatory Affairs · Job Title: Manager, Regulatory Affairs · Serves as a liaison with regulatory agencies and contractors. · Evaluates regulatory documents for submission to governmental regulatory agencies li ...