Regulatory Affairs Associate

7 months ago


Uxbridge, United Kingdom Proclinical Full time

Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or Cambridge.

**Key Skills and Requirements**:

- Familiarity in an administrative field within a corporate or similar setting preferably within a healthcare sector.
- Educated to a degree level in a scientific field would be ideal.
- Demonstrable experience in CTA linked work assisting medicinal products.
- Familiarity with writing or updating procedures would be ideal.
- Capable of learning in a swift manner.
- Able to be flexible and adaptable to alterations.
- Expertise on regulatory CTA needs and the role of regulatory affairs as these pertain to medicinal product trials, which involves expertise and comprehension of ICH standards and varying regional needs in the allocated markets.
- An organised individual with a high attention to detail.
- Computer literacy.
- Project management abilities with the capacity to handle various tasks simultaneously.
- Communication skills both verbally and in writing in both a clear and concise manner.
- Works well in a team within a highly matrixed setting.
- Able to complete various tasks allocated.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

Regulatory



  • Uxbridge, United Kingdom CV-Library Full time

    CK Group have an opportunity for a Senior Associate in Regulatory Affairs, to join a global pharmaceutical company on a 12-month contract basis. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This...


  • Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group have an opportunity for a Senior Associate in Regulatory Affairs, to join a global pharmaceutical company on a 12-month contract basis.Company:Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron Pharmaceuticals Inc. is seeking a highly skilled Regulatory Affairs Senior Associate to join our team.Job Summary:The Regulatory Affairs Senior Associate will be responsible for performing regulatory assessments of changes, interpreting the current, approved, and planned clinical regulatory landscape by...


  • Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron Pharmaceuticals Inc. is seeking a highly skilled Regulatory Affairs Senior Associate to join our team.Job Summary:The Regulatory Affairs Senior Associate will be responsible for performing regulatory assessments of changes, interpreting the current, approved, and planned clinical regulatory landscape by...


  • Uxbridge, United Kingdom CK Group Full time

    CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. **Job...


  • Uxbridge, United Kingdom CK Group Full time

    CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. **Job...


  • Uxbridge, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Uxbridge, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time

    Senior Associate Regulatory AffairsCK Group- Science, Clinical and Technical is seeking a highly skilled Senior Associate Regulatory Affairs professional to join their team on a 12-month contract basis.About the Role:This is an exciting opportunity to provide European regional regulatory leadership and expertise for the development, registration, and...


  • Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time

    Senior Associate Regulatory AffairsCK Group- Science, Clinical and Technical is seeking a highly skilled Senior Associate Regulatory Affairs professional to join their team on a 12-month contract basis.About the Role:This is an exciting opportunity to provide European regional regulatory leadership and expertise for the development, registration, and...


  • Uxbridge, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs Consultant - CMC small moleculeParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs...


  • Uxbridge, United Kingdom Parexel Full time

    Join Our Team as a Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project management...


  • Uxbridge, United Kingdom Parexel Full time

    Join Our Team as a Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project management...


  • Uxbridge, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Uxbridge, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. In this role, you will be responsible for performing regulatory assessments of changes and interpreting the current, approved, and planned clinical regulatory landscape.Key Responsibilities:Regulatory Submission Review:...