Freelance Clinical and Regulatory Start Up Manager
Nr ref.: /JOBS.pl
Role: Clinical and Regulatory Start Up Manager
Location: Anywhere in Europe
Contract: 6 months - 1 year
Are you looking for a change? Looking to make a difference, check us out!
Premier Research helps highly innovative biopharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research
We're looking for a strong Freelance Clinical and Regulatory Start Up Manager to join our team! You will be required to ensure the continuous improvement of quality of all Regulatory and Start-up components at the project level. This is a global position and can be located anywhere in Europe.
You will need to start immediately and have 0.5 - 1.0 FTE availability.
You'll be accountable for:
Preparing Core Clinical Trial Applications for competent authorities Driving the overview of applications done by Start-up Managers to competent authority (CA) and Ethics Committees /IRBs Producing or reviewing some submission components like the Patient Information Form/ICF and or Investigational Medicinal Product Dossier (IMPD) or equivalent document as required Maintaining good, friendly and professional relationships with past, current and potential sponsors Contributing to the business development process by reviewing proposals, budgets and attending client meetings Keeping abreast of scientific developments and maintain technical expertise Working with the PM to understand financial aspects of the project; cascades to all start-up team members the number of hours/tasks available per contract; monitoring project performance
You'll need this to be considered:
Education to university degree level in pharmacy, medicine or related natural sciences Strong experience, including previous experience in Regulatory or Start-up functions ideally on a global level Hands-on experience in the submission of clinical trial applications Ability to multitask and work effectively in a fast-paced environment with changing priorities Maintains a positive, results orientated work environment Ability to read, write, and speak fluent English
If you are looking for a career within a transparent and non-hierarchical organisation then please contact us at the email address listed below. We are open minded and flexible regarding the talent we recruit, ultimately we are looking for people who will share in our vision and realise the importance of communication, building relationships and adhering to the highest quality standards.
Please note:- You must be eligible to live and work in the specified European country in order to apply for this role.
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