Clinical Dynamix

Great way to end the week- One of our clients received FDA approval on their Rare Cancer Drug!!! We are grateful to ALL our Life Science clients who partner with us to build strong R and D teams!! Right now we have clients who are adding new critical needs: Director/Senior Director Medical Writing (Regulatory) - Remote (US based) Clinical Trial Managers- Massachusetts ED, Toxicology- CA Continuous Improvements Manager roles- SouthEast Quality CMC - NJ Senior Manager, Clinical Data-MA Quality Assurance- NJ ....and more.....reach out to us at www.clinicaldynamix.com #hiring #clinicaldevelopment #medicalaffairs #medicalwriting #regulatoryaffairs #biotech #pharmaceutical #medicaldevice #diagnostic #researchanddevelopment #lifesciences #jobs

HAPPY AND HEALTHY 2024! Our clients are passionate Biotech and Device companies, researching each day for cures to ensure a future full of "health" in the world.... We have current needs for: a Clinical Scientist Consultant, Oncology a Manager, Regulatory Affairs a Pharmacometrician a Medical Director, Neurology....and more! apply on our website or reach out if you are looking for a new role (....and to make a difference in the year ahead!!!)! #jobsearch #pharmaceutical #biotech #medicaldevices #diagnostics #hiring #jobopening #jobseeker #talentacquisition #clinicalresearch #clinicaloperations #medicalaffairs #researchanddevelopment #clinicaldynamix

TWO FOR TUESDAY! 1. Are you a seasoned Director of Toxicology? One of our biopharmaceutical clients is expanding! 2. Are you a seasoned Senior Director, Global Regulatory with small molecule experience? One of our pharmaceutical clients is looking for a dynamic leader to join their team! contact me for more information #hiring # jobsearch #job #regulatoryaffairs #toxicology #clinicaldevelopment #clinicaloperations #pharmaceutical #medicalaffairs #clinicalresearch #researchanddevelopment #jobs #talentacquisition #recruitment #recruiter

Monday morning mention! Our clients are hiring: East Coast based Director, Clinical Operations - if you have hematology and oncology (late phase through commercial)- reach out to me or my team- would love to share our latest need :) We also have Regulatory, Senior Director roles - must have Global Submissions experience (full life cycle - late phase and post marketing) in Small molecules Clinical Trial Manager Contract (hybrid role in Lexington, MA) DMPK Senior Director (San Diego - robust relocation package) and more.... www.clinicaldynamix.com #jobsearch #hiring #jobopening #talentacquisition #clinicaloperations #clinicaldevelopment #regulatoryaffairs #medicalaffairs

San Francisco Bay area Biotech Client, with outstanding leadership and Innovative Science, has the following immediate need: Medical Director, Vaccines: Will serve as the Lead for Vaccine development strategy and execution of Clinical Trials. Must be a M.D. or M.D./Ph.D. and have at least 4 years’ Industry Clinical Development experience preferably in Vaccine Development including 3+ years’ experience leading cross functional teams and management experience. Client prefers candidates to be local in the Bay area but is open to a Hybrid or Remote scenario for the right candidate! Competitive compensation package is offered including excellent benefits! Please inquire asap for complete details! [email protected]. #ClinicalDynamix #medicaldirector #clinicaldevelopment #vaccines #toptalent #medicaldoctor

Northern New Jersey Biotech Client has a Sr. Manager, Quality Assurance position available (Hybrid role in office at least twice a week)!   The successful candidate will be responsible for (amongst other duties): Management and Maintenance of the Veeva Quality Docs System, including document drafting/Authoring, reviewing, approving, and finalizing internal quality documents (SOPs, investigations, etc.). Provide authorship/review/approval of additional SOPs/policies for GMP/GCP regulatory compliance, where there may be gaps identified. Hands on experience with Electronic Document Management System (Veeva preferred), managing documents lifecycles-Draft to Effective/approved, Initial to Final and Periodic Review. The successful candidate has: A B.S. Degree and 7-10 years of Industry experience with 5+ years working within the Quality Assurance/Quality Systems, Clinical Operations, and/or Regulatory environment in the pharmaceutical or biotechnology industry. Please inquire ASAP for complete details! [email protected]; www.clinicaldynamix.com #qualityassurance #cmc #qualitysystems #cqa #veeva #toptalent #ClinicalDynamix