Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.

May assist in the preparation for regulatory agency site visits.

For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. In th...

May assist in the preparation for regulatory agency site visits.

For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. In th...

Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...

May assist in the preparation for regulatory agency site visits.

May assist in the preparation for regulatory agency site visits.

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.Assists in preparing grant...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.Assists in preparing grant...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.Assists in preparing grant...

Assist regulatory personnel with completion and filing of regulatory documents. The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the proces...

The Clinical Research Coordinator I will direct participants and study team members to adhere to the study protocol and rules and regulations as governed by regulatory bodies including Institutional R...

Directing strict adherence to the study protocols, as well as sponsor, FDA and other regulatory authority requirements. The Clinical Research Coordinator I will direct participants and study team memb...

Assist regulatory personnel with completion and filing of regulatory documents. The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the proces...

Global - Responsible for the overall product strategy, global reporting, administrative documentation, due diligence, market expansion, labeling content, regulatory compliance, regulatory intelligence...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. This i...

The Coordinator develops and maintains recordkeeping systems and procedures for the research study including data collection forms, databases, participant research files, and regulatory files. Serves ...

Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...

Serves as main liaison for the study team, study sponsor, applicable regulatory agencies, and facility Research Department leadership. Trains study team on protocol and regulatory procedures; responsi...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. This i...

The Senior Regulatory Affairs Specialist will work in BD Specimen Management providing regulatory leadership to cross-functional project teams from early development to new product launches in variou...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. Docume...

The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. This i...

Technology Regulatory Affairs Specialist.

Technology Regulatory Affairs Specialist.

The primary goal of this research project is to study the cognitive health of older Chinese Americans.Participants will undergo a standard dementia evaluation that includes a medical exam, cognitive t...

The Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies.Web link ...

Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol. Monitors all study act...

Completes mandatory regulatory and study-specific trainings.

This includes assessing CMC changes during development and defining regulatory CMC requirements, demonstrating sound regulatory insight, ensuring a balanced approach to regulatory risk, utilizing regu...

This includes assessing CMC changes during development and defining regulatory CMC requirements, demonstrating sound regulatory insight, ensuring a balanced approach to regulatory risk, utilizing regu...

The role assists the Regulatory Manager and other associates within the Regulatory Department and works internally with Product Development, Sales/Customer Service and other internal functional areas ...

Working knowledge of relevant federal and state regulatory programs (e.

Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as neces...

Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as neces...

We are seekinga Senior Scientist - Regulatory tojoin our Regulatory team inour Clark, NJ Researchfacility. As a SeniorScientist - Regulatory in our Regulatory team, your main responsibilitiesare:. Pos...

We are seekinga Senior Scientist - Regulatory tojoin our Regulatory team inour Clark, NJ Researchfacility. As a SeniorScientist - Regulatory in our Regulatory team, your main responsibilitiesare:. Pos...

Regulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...

This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Stra...