- Regulatory Affairs CMC Bio Contract - Near Heathrow - options to work 2 days a week from Home
12 month contract based in Maidenhead or Uxbridge - Options to work 3 days in the office and 2 days a week from home. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
- Medical Writing & Publication Manager - 3 days/week - Monday to Wednesday - 12 month Fixed Term Contract
Who we are
We’re innovation, curiosity and diversity – multiplied by 92,500 professionals in 150 countries. As a global leader in research-focused healthcare, we’re constantly learning and growing – and seeking people who share these goals. ...
- Associate Clinical Trial / Study Manager – 12 Month Contract – South East England – £320 per day
We are recruiting for an Associate Clinical Trial/Study Manager for a 12 month contract, office based in South East England. The role will be a supporting position for the Study Manager, managing vendors and dealing with budgets and timelines. The contract has a very strong likelihood of extensions and would be a great step up for a Lead CRA or Associate Study Manager, at an industry-leading company.
- CMC Project Leader (m/w) - Freelance
CMC Project Leader (M/W) - FreelanceEurope€100.00 Per Hour The opportunityI am currently working with a growing Biotech who are looking for an experienced CMC Project leader on a freelance basis. These can be based anywhere in Europe, however you must be able to travel to Frankfurt for the first 2-3 weeks SOP training. The ideal candidate will possess the following; * At least 5 years experience in CMC regulatory project management. * Expertise in Quality and risk management. ...
- Clinical Trial Manager – 12 Month Contract - £400+ per day - Pharma
We are looking for an experienced individual to work as a Clinical Trial Manager for a niche biotech. CRO management will be a large part of the role so experience in this is key. This role is office based in the South East and is an initial 12 month contract. This is a great chance to join an exciting team with a growing pipeline and with a high chance for contract extension and professional development within a contract.
- Contract CTA / Clinical Trial Assistant – 12 Months – Global Pharma - £180+ per day
We are looking for a Study Delivery Administrator (CTA) to be based in Bedfordshire for a global pharma. The position is office based and the contract is for 12 months. The role will focus on supporting the Study Delivery Teams and archiving of study documentation. This is a great opportunity for an experienced CTA to join an internationally respected pharmaceutical company.
- Permanent Part-Time CRA role - Stockholm (3-4 days as week)
Background:Small CRO won a new long-term business with a International sponsor and now is looking to hire a permanent CRA's. Ideally they would be keen on full time permanent people but could be open for candidates with 3-4 days of availability. It is a office based position in Stockholm.This is a role for experience CRA with strong monitoring experience, as well as Regulatory submissions background. ...
- Project Manager – Ops/R&D – Noord-Brabant (12 months)
Keywords: Project Managers, Project Operations Manager, R&D, Drug Development, CRA, Consultancy, Operations, Pharmocodynamics, pharmacokinetics, Toxicokinetics, process validation, CMO, CRO, project, engineer, inginieur, technoloog, interim, freelance, tijdelijk, contractor, pharma, R&D, Master, PhD, Bachelor, Location: Noord-BrabantType: Contract/freelanceDuration: 12 monthsStart date: ASAPDays per week: 5 days per week, possibility 1 or 2 home-basedDo you want to be part of a large gr ...
- Product Manager - Specialist Care - London
Our client is one of the few pharmaceutical groups in the world to master various advanced bioproduction techniques, and is an expert in plasma-derived medicinal products, ranking 6th worldwide and 1st in France in this field.They are currently seeking a Product Manager to take on responsibility for brand management of their rare disease/specialist care portfolio.
- Clinical Operations Team Leader
ROLE TITLE: CLINICAL OPERATIONS TEAM LEADERROLE INTRODUCTION: Sit in-house at a well-regarded pharmaceutical company, as a Clinical Operations Team Leader as a representative of their preferred supplier of clinical research services.You will work closely with senior directors to scope clinical operations objectives for EU and global clinical trials. Managing CRA project teams, you will hold responsibility for the performance of Clinical Operations across your assigned projects. ...