Regulatory Affairs Associat CMC contract
JOB_52040444537638Job type
ContractLocation
UxbridgeWorking Pattern
Flexible Working,Full-timeSpecialism
Regulatory AffairsIndustry
PharmaceuticalsPay
£16 - £19 per hour umbrellaClosing date
6 Jun 2024
Regulatory Affairs Associate, CMC, contract job, hybrid working, uxbridge
Regulatory Affairs Associate CMC
Your new company
Your new role
What you'll get in return
Flexible working options are available.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
Your new company
This well known biotech are looking for a Regulatory Affairs Associate on a contracting basis to join their established CMC team in Uxbridge
This is a 12 month contract job. This well known biotech are looking for a Regulatory Affairs
Associate on a contracting basis to join their established CMC team in Uxbridge
This is a 12 month contract job
Your new role
The Associate Regulatory Affairs (CMC) provides varying levels of product support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across phases of product development from clinical to lifecycle. Support may include organising, managing and executing on regulatory CMC projects and submissions. Tasks may include creating and/or maintaining submission timelines and tables of contents, formatting of documents per style guide, scheduling meetings, drafting meeting agendas and minutes, managing document reviews and other tasks as requested.
• proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
• strong organisational skills with attention to detail;
• excellent time management skills and ability prioritize workload;
• project management skills;
• adept interpersonal and communication skills (both verbal and written);
• ability to work both independently and as a member of a team. The Associate Regulatory Affairs (CMC) provides varying levels of
Product support to the Chemistry, Manufacturing and Controls (CMC) function,
Which is responsible for Module 3 of regulatory submissions across phases of
product development from clinical to lifecycle. Support may include organising,
Managing and executing on regulatory CMC projects and submissions. Tasks may
include creating and/or maintaining submission timelines and tables of
contents, formatting of documents per style guide, scheduling meetings,
drafting meeting agendas and minutes, managing document reviews and other tasks
as requested.
What you'll need to succeed
• proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
• strong organisational skills with attention to detail;
• excellent time management skills and ability prioritize workload;
• project management skills;
• adept interpersonal and communication skills (both verbal and written);
• ability to work both independently and as a member of a team.
• proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
• proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
• strong organisational skills with attention to detail;
• excellent time management skills and ability prioritize workload;
• project management skills;
• adept interpersonal and communication skills (both verbal and written);
• ability to work both independently and as a member of a team.
What you'll get in return
Flexible working options are available.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
Regulatory Affairs Associat CMC contractJOB_520404445376382024-03-232024-06-06
Talk to Victoria Dunlop, the specialist consultant managing this position
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JOB_52040444537638