Vivid Resourcing Jobs in United States

We are seeking a highly experienced Vice President, Regulatory Affairs, CMC to provide strategic and operational leadership for global CMC regulatory activities across a growing pipeline of innovative therapeutics. · We seek a recognized subject matter expert in Regulatory Affair ...

The Senior IAM Consultant will lead identity engagements from discovery through solution design, implementation, and closeout. · ...

We are seeking a highly experienced Senior Vice President, CMC Regulatory Affairs to provide strategic and operational leadership for global CMC regulatory activities across a growing pipeline of innovative therapeutics. · This role is designed for a recognized subject matter exp ...

We are seeking a Network Security Engineer to join a large-scale enterprise environment responsible for designing implementing and securing complex network infrastructures across on-prem and cloud environments. · ...

Senior Vice President–level Regulatory Affairs Consultant to provide high-level regulatory oversight across a rapidly expanding portfolio. · Define and approve global regulatory strategy. · Oversee preparation of INDs, NDAs, BLAs, and international submissions. · ...

A leading biotech company in Boston seeks a Chief Medical & Regulatory Officer (CMO) to oversee clinical and regulatory strategy. The ideal candidate will have over 15 years of experience in the biotech/pharma sector, particularly in regulatory affairs, and possess an MD or equiv ...

This Global Regulatory Lead role owns regulatory strategy end-to-end across assigned programs and plays a visible role in shaping development, approval, and lifecycle decisions. · ...

body{font-family:Arial;}h1{color:#00698f;}h2{color:#4CAF50;}Clinical Data Research Associate · The Vivid Resourcing Team is seeking a highly motivated and detail-oriented Clinical Data Research Associate to support the planning, execution, and monitoring of oncology clinical tria ...

Director, Regulatory Affairs – Rare Disease · Boston, Massachusetts | Hybrid · Company Overview · An innovative clinical-stage biopharmaceutical company developing genetic medicines for rare diseases is seeking a Director of Regulatory Affairs to support global regulatory strateg ...

We are hiring Field Sales Representative to support the growth of our PUDO network across South Belgium and Luxembourg by building strong partnerships with local retail stores. · ...

The Clinical Research Associate (CRA) will support the planning, execution,and monitoring of oncology clinical trials in compliance with ICH-GCP,FDA regulations,and company SOPs. · Bachelor's degree/Master's degree in Life Sciences,Nursing, · or a related field (required) · , 2+ ...

Senior Manager, Regulatory Affairs for Gene Therapy at Vivid Resourcing · About Us: · We are a pioneering biotech company dedicated to developing breakthrough gene therapies for rare and orphan diseases. Our mission is to transform patients' lives by advancing innovative therapie ...

Director, Regulatory Affairs – Rare Disease · Boston, Massachusetts | Hybrid · Company Overview · An innovative · clinical-stage biopharmaceutical company developing genetic medicines for rare diseases · is seeking a · Director of Regulatory Affairs · to support global regulatory ...

A great opportunity with a fast growing tech client in the Centre of New York · About the role · We are looking for a SDR & BDR Manager, responsible for driving outbound and inbound pipeline generation. You will lead a team of six SDRs and BDRs, with the potential to grow as we s ...

Hands-on CyberArk PAM (Vault, CPM, PSM, PSMSession, plugins) · Privileged account onboarding & lifecycle management · Strong understanding of IAM / security principles · ...

Our client is seeking a Medical Director or Senior Medical Director to provide scientific and clinical leadership across key development programs. · ...

We are seeking a highly accomplished Senior Vice President–level Regulatory Affairs Consultant to immediately join our executive leadership function and provide high-level regulatory oversight across a rapidly expanding portfolio.This opportunity is designed for an elite regulato ...

Drug Safety Manager · This role plays a key part in the development and execution of risk management activities across clinical programs at Vivid Resourcing's innovative biotech client. · The Role: · We are looking for someone with strong scientific judgment, structured thinking ...

We are seeking a Senior Cyber Security Consultant specializing in Incident Response to lead and execute complex security investigations in high-pressure environments. · Lead and coordinate complex incident response engagements from detection through remediation · Mentor and suppo ...

We're partnering with a leading Boston-based oncology biotech to find a Senior Director of Regulatory Affairs to lead global regulatory strategy across their clinical development pipeline. · ...