Company: Apsida Life Science
Job Title: Regulatory Project Manager
Location: Ireland & UK Regulatory Affairs – Fully Remote
Duration: 6–12 months
Experience: Pharmaceutical/Regulatory Affairs experience required
Qualification: Graduate/PhD in Life Sciences or equivalent
Job Type: Contract / Project-based
Posted: September 7, 2026
Author: Pharmabharat Editorial Team
Regulatory Project Manager Job – Apsida Life Science
Apsida Life Science is partnering with an organisation focused on community-based clinical trials and high standards of participant care. The organisation is looking for an experienced Regulatory Project Manager to support regulatory activities across Ireland and the UK.
This is a fully remote regulatory affairs opportunity for professionals with pharmaceutical industry experience and a strong understanding of national and/or EU regulatory requirements. The assignment is expected to run for 6–12 months and will involve regulatory management of clinical assets and Marketing Authorisations (MAs) across a portfolio of products.
The role may suit professionals with experience in pharmaceutical regulatory affairs, regulatory submissions, Marketing Authorisation maintenance, product information, regulatory agency interactions and compliance.
Job Highlights
- Position: Regulatory Project Manager
- Company: Apsida Life Science
- Work Location: Ireland & UK Regulatory Affairs
- Work Mode: Fully Remote
- Contract Duration: 6–12 months
- Education: Graduate/PhD level or equivalent in Life Sciences
- Industry: Pharmaceutical / Life Sciences
- Focus: Regulatory Affairs, Marketing Authorisation and Product Compliance
Regulatory Project Manager Responsibilities
The selected candidate will be responsible for managing regulatory activities and supporting the maintenance of clinical assets and Marketing Authorisations for products in Ireland and the UK.
Key responsibilities include:
- Manage the delivery and maintenance of clinical assets and Marketing Authorisations (MAs) for a portfolio of products in Ireland and the UK.
- Ensure product information remains compliant with applicable Marketing Authorisations and regulatory requirements.
- Review and maintain Summary of Product Characteristics (SPCs) and Patient Information Leaflets (PILs) and ensure applicable labelling remains compliant.
- Coordinate national input for responses to regulatory questions and regulatory commitments.
- Ensure regulatory responses align with approved regulatory strategies, requirements and agreed timelines.
- Manage product registration documentation within relevant regulatory databases and repositories.
- Coordinate and manage correspondence with regulatory agencies in accordance with company procedures.
- Ensure regulatory agencies are notified promptly about relevant product quality and safety issues.
- Complete Marketing Authorisation Holder (MAH) reviews of Periodic Quality Reviews for registered products for which the company is the Ireland MAH.
- Plan regulatory activities effectively across the assigned product portfolio.
- Provide regulatory advice, leadership and subject-matter expertise to brand teams and other regulatory and cross-functional groups.
- Support regulatory governance and ensure activities are conducted in accordance with applicable procedures and requirements.
Qualifications for Regulatory Project Manager
Candidates should have a Graduate or PhD-level qualification, or equivalent, in Life Sciences.
The preferred candidate should also have:
- Previous experience in the pharmaceutical industry.
- Professional experience in regulatory affairs.
- Strong understanding and practical experience with national and/or EU regulations, guidelines and regulatory working practices.
- Knowledge of regulatory issues relevant to the assigned portfolio.
- Understanding of the drug development process and regulatory affairs.
- Awareness of commercial and medical considerations associated with pharmaceutical products.
- Understanding of competitor products and activities relevant to the assigned portfolio.
- Strong knowledge of regulatory governance, medical and safety requirements.
- Ability to provide regulatory guidance and work effectively with cross-functional teams.
- Strong communication, organisation and project-management skills.
Skills That Can Help You Succeed
Professionals applying for this UK and Ireland Regulatory Affairs job should ideally be comfortable working independently in a remote environment. Experience with Marketing Authorisation maintenance, regulatory documentation, product information, regulatory agency correspondence and pharmaceutical compliance can be particularly relevant.
Knowledge of EU and national regulatory frameworks will also be valuable for this regulatory project management position.
Benefits and Career Opportunity
The supplied vacancy does not specify a formal benefits package. However, the role offers several professional advantages:
- Fully remote working arrangement.
- Exposure to UK and Ireland regulatory affairs.
- Opportunity to work with pharmaceutical and life science stakeholders.
- Experience managing regulatory activities across a product portfolio.
- Exposure to Marketing Authorisation maintenance and regulatory compliance.
- Opportunity to work on a 6–12 month regulatory project.
- Cross-functional interaction with regulatory, medical, safety and brand teams.
Salary: The original vacancy does not disclose compensation. For structured-data purposes, an estimated equivalent range of ₹45,00,000–₹75,00,000 per year has been used based on the seniority and specialist nature of the role. Applicants should confirm the actual compensation, currency and contractual terms directly with the recruiter.
How to Apply for Apsida Life Science Regulatory Project Manager Job
Interested candidates can contact Sweetness Zono at Apsida Life Science to learn more about the Regulatory Project Manager opportunity and application process.
Email: Sweetness.zono@apsida.com