Regulatory Content Strategist; Project Manager

Position: Regulatory Content Strategist (Project Manager) (Contract)
Location: Welwyn Hatfield

Job Opportunity:
Regulatory Content Strategist (Project Manager)

Location:

Welwyn (Hybrid)

Contract:

12 months
Rate: £60 - £75 per hour (umbrella) OR £45.50 - £56.40 per hour PAYE

Are you passionate about shaping the future of healthcare? Join our dynamic team as a Regulatory Content Strategist (Project Manager) and make a meaningful impact on patients' lives!

At our organization, we strive for a healthier future by advancing science and innovation. As part of the Pharma Development Regulatory (PDR) team, you will play a pivotal role in developing and executing content strategies that facilitate the approval of groundbreaking therapies and devices.

What You'll Do:

Lead with

Purpose:

Manage a team of Content Strategists and cross-functional teams to develop and execute comprehensive content strategies for submissions to global regulatory authorities, ensuring adherence to applicable guidelines and internal standards.
Strategic Planning:
Create and manage timelines for document production and review, aligning with overall project goals to ensure timely submissions.
Quality Assurance:
Review documents for clarity, organization, scientific integrity, and consistency. Collaborate with contributors to resolve issues and ensure compliance with regulatory requirements.
Collaborative Partnership:
Actively participate in functional and cross-functional teams, contributing to best practices and continuous improvement initiatives. Partner with key stakeholders to shape our technical, business, and healthcare strategies.
Stay Ahead:
Maintain up-to-date knowledge of relevant regulatory, scientific, and medical topics in drug development and therapeutic areas.
Mentor & Guide:
Act as a mentor to new or less experienced Content Strategists, fostering a culture of learning and development.

Who You Are:

Educational Background:

Degree in Life Sciences or equivalent with relevant experience in the pharmaceutical/biotechnology industry.
Experienced Leader:

Proven experience in leading cross-functional teams and delivering independent projects successfully.
Regulatory Knowledge:

Familiarity with regional and global drug and device development processes, regulations, and guidelines (e.g., GxP, GCP, ICH, ISO, MDR/IVDR).
Documentation Expertise:

Demonstrated experience in clinical, safety, and device regulatory documentation throughout the product lifecycle.
Analytical Thinker:

Strong ability to analyze and synthesize complex data and concepts from various disciplines.
Effective Communicator:

Exceptional interpersonal skills with a knack for fostering collaboration and resolving conflicts in matrixed environments.
Tech-Savvy:

Proficient in G Suite, Microsoft Office Suite, Adobe Acrobat, and Veeva Vault, with a detail-oriented approach and a creative mindset.

Why Join Us?

By joining our organization, you'll be part of a bold and innovative team that values your contributions and encourages professional growth. We believe in fostering a collaborative environment where every voice matters and every idea counts.

If you're ready to take on this exciting challenge and help shape the future of healthcare, we want to hear from you!

Apply now to become our next Regulatory Content Strategist and be a part of something extraordinary!

Don't miss this chance to make a difference-your journey to influence the future of healthcare starts here!

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.

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Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

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