Indegene is seeking a Content Operations & MLR Coordination Specialist for a 2-month contractual project in Perugia, Italy. This role will ensure the efficient delivery of promotional materials through the MLR approval process, facilitating collaboration across Marketing, Regulatory,
Role Overview In a fast‑paced, customer‑centric environment, we are looking for a Content Operations & MLR Coordination Specialist to ensure the efficient, accurate, and timely delivery of promotional materials through the MLR approval process. This role is critical
Independent Investment Advisor Balfour Capital Group This is an independent contractor engagement. Compensation is structured on a commission-only, production-linked basis; no base salary or guaranteed income is associated with this role. Candidates should have established client
Content Operations & MLR Coordination Specialist (Veeva PromoMats) Contractual: 2‑month project. Role Overview In a fast‑paced, customer‑centric environment, you will ensure the efficient, accurate, and timely delivery of promotional materials through the MLR approval process. This role accelerates
Job Summary The Clinical Study Manager (CSM) will be part of the Clinical Operations Department, which is responsible for planning, executing, managing and closing studies associated with the company clinical development plans. The CSM is a
Indegene is seeking a Content Operations & MLR Coordination Specialist for a 2-month project in Terni, Italy. You will manage the MLR approval process to ensure timely delivery of promotional materials. The role involves coordinating among Marketing and
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical
Secondary Permitting Manager – Renewable Energy / Utility Scale ProjectsPer una comprensione completa di questa opportunità e dei requisiti per essere un candidato di successo, continui a leggere.We are looking for a Secondary Permitting Manager to
Chief Machinery and Packages Engineer | Take Project Ownership at ArkadPossiede le qualifiche e le competenze giuste per questo lavoro? Lo scopra qui sotto e invii la sua candidatura per essere preso/a in considerazione.Are you a
With more than 150 years of industry-leading experience, the businesses of SGS & Co and SGK are uniting to form SGX—a powerful force in innovative packaging production. Building on the legacy of trusted service since 1947
If you are interested in the field of Commercial Excellence and you would like to work in a young and dynamic company, this is your opportunity! As RGM Expert you will support RGM Promo Lead to
Select how often (in days) to receive an alert: Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Date: 17 Mar 2026 Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job
Job Title : Medical Director, Oncology Location : Rome, Italy (Home based – any Italy location considered) Shape the future of oncology drug development Caidya, a mid-sized global CRO, is seeking a Medical Director with experience
If you are interested in the field of Commercial Excellence and you would like to work in a young and dynamic company, this is your opportunity! As RGM Executive you will support the RGM Promo Lead
With more than 150 years of industry-leading experience, the businesses of SGS & Co and SGK are uniting to form SGX—a powerful force in innovative packaging production. Building on the legacy of trusted service since 1947
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice
Date: 10 Feb 2026 Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Senior Manager, CMC Regulatory Affairs, Global Rare Diseases About us Chiesi
# Supplier Lead, Commercial AircraftApplyremote type: Fully Remote or Hybrid if Locallocations: Genova, IT: Memmingen, DE: Amsterdam, NL: Nuremberg, DE: Toulouse, FRtime type: Full timeposted on: Posted Todaytime left to apply: End Date: July 31, 2026
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Date: 17 Mar 2026 Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT