About Us Based in Parma, Italy, Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in 31 countries. More than 8,000 employees across the group are united by a singular purpose: promoting a
Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug
About KOHO We’re on a mission to make financial services better for every Canadian. That means no hidden fees, no predatory interest rates - just financial products designed to help our users spend smart, save more,
Please do not apply if you are not fully eligible to work in Australia. CTI doesnt offer any Sponsorship. What you’ll do: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to
About Cristcot We are in the business of addressing the problem within the problem. We focus on the details and connections that other, major pharma companies have left ignored for years. There are better ways, better
This role sits at the intersection of regulatory privacy and compliance, health plan operations, and revenue cycle integrity. The Senior Regulatory Compliance & Revenue Cycle Analyst is responsible for advancing compliance across payer relationships, reimbursement practices, and healthcare
Job Purpose/ Summary: Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with, assist, and advise
About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for
General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, CA, USA Onsite or Remote Fully Remote Work Schedule Monday - Friday, 6:00 AM - 3:00 PM PST Posted Date 07/21/2026
Regulatory Strategist Program Manager( Job Number: 40584) Description University of Colorado Anschutz Department: OVCR Investigational New Drug/ Device Office Job Title: Regulatory Strategist Program Manager Position #: 846482 – Requisition #: 40584 Job Summary: Reporting to the Assistant
Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must
Job Description The Chemistry Manufacturing Controls Manager will be responsible for the detailed planning, preparation and operational execution of a multi-product program in the international region. This role contributes to the preparation and submission of regulatory CMC
*THIS POSITION IS NOT ELIGIBLE FOR VISA SPONSORSHIP * To be considered for this position, applications and resumes are accepted only through our careers site by directly applying to the posted job. We do not accept
Company:Guy Carpenter Description: We are seeking a talented individual to join our Underwriting Analytics team at Guy Carpenter. This role can be located on a hybrid basis in any Guy Carpenter office or be remote. The
Sr. Medical Writer (Regulatory) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity,
Cascade Engineering Services is looking for a candidate with experience in Regulatory Compliance in areas of EMC (Electromagnetic Compatibility), RF (Radio Frequency) and Safety. The Regulatory Certifications Program Manager will be a part of a Global Certifications team
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on
Description Monroe Group is looking for a Regional Compliance & Legal Coordinator in our Denver office. This is a hybrid position: three days in the office, two remote. JOB SUMMARY: The Regulatory Compliance & Legal Coordinator supports
Global Documentation and Lifecycle Lead – Standard Materials Hyderabad, India The Global Documentation and Lifecycle Lead – Standard Materials plays a critical role in ensuring compliant, efficient, and harmonized document lifecycle management across Lonza’s global network. This is
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical