Clinical Regulatory Affairs Specialist, you will play a critical role in managing essential documentation and regulatory... success of clinical trials by overseeing the submission of regulatory packages, managing IRB approvals and amendments...
About the Job The Senior Specialist, Regulatory Affairs performs activities to support the regulatory submissions... for regulatory agencies and ensures compliance with all requirements. Key Responsibilities Represent the regulatory affairs...
ecosystem to drive better health outcomes. Description As a Principal Regulatory Affairs Specialist at Verily, you will work... directly with other Regulatory Affairs team members, partners and a team of experts from diverse fields (e.g., Biology...
to comply with regulatory requirements for clinical trials. Contributes to the development, review and maintenance of standard... Provides information on regulatory requirements to assigned disease program partners. Interacts with other clinical trials...
solutions that make a difference in patients' lives. Position Summary The Clinical Affairs Specialist, MCS augments the..., with experience using IABPs. Previous experience as a Clinical Specialist in industry is desirable. Have current licensure...
Specialist supports regulatory compliance for clinical research at Beth Israel Deaconess Medical Center (BIDMC...: Bachelor's degree required; Master's degree preferred in Regulatory Affairs. 1-3 years related work experience...
Safety, Regulatory Affairs and Medical Affairs Lead and participate in activities that ensure quality, consistency... pharmaceutical industry. Preferred Qualifications For MD, at least 3 years clinical experience from a specialist position...
, Regulatory Affairs, Drug Safety, and Medical Affairs. Our products are utilized by 40 out of 50 major biopharmaceutical companies... delivery of life-saving medications. As an industry leader, ArisGlobal offers software as a service for Clinical Trials...
. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials...Global Market Access & Pricing Specialist - VIE Contract Location: USA, Cambridge Target start date: 01/02/2025...
standards for editing and formatting Working knowledge of clinical development and regulatory affairs documentation Experience... performing in-depth quality control (QC) reviews on moderately complex clinical and regulatory documents across multiple...
research and/or regulatory affairs. Knowledge of federal, state, and local laws and regulations governing human subjects.... General Overview The Expedited Specialist II will conduct reviews of submitted human subject research applications in...
-engineering, Life Sciences, Regulatory Affairs, or related discipline. Master's degree preferred. Minimum of 5-years' experience...As a Medical Device Compliance Specialist, you will play a critical role in helping departments across the company...
, as well as with our organization's clinical research policies. The responsibilities of the Compliance Specialist include but are not limited... responsibilities of sponsor-investigators related to IND and IDE regulatory requirements, annual reporting to the FDA, and Clinical...
The Assisted Living Certification Unit of the Executive Office of Elder Affairs (EOEA) is responsible for the... certification and regulatory oversight of approximately 271 Assisted Living Residences (ALR’s) statewide. The Registered Nurse...
Affairs. Support, update and maintain the Clinical Trial Management System application for clinical study execution..., but is not a supervisor Qualifications You are: 3 plus years of clinical monitoring Knowledge of ICH and local regulatory authority...
Affairs. Support, update and maintain the Clinical Trial Management System application for clinical study execution..., but is not a supervisor Qualifications You are: 3 plus years of clinical monitoring Knowledge of ICH and local regulatory authority...