Senior Manager, Regulatory Affairs

Summittherapeutics; Oxford; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Senior Manager in Regulatory Affairs to oversee regulatory activities for clinical trials and submissions. This role demands a proactive leader with extensive experience in the pharmaceutical sector, particularly in navigating EMA regulations and managing complex projects. The ideal candidate will possess a strong educational background in biological sciences and a proven track record in regulatory affairs. Join a dynamic team dedicated to advancing healthcare solutions while enjoying the benefits of a supportive work environment. This is an exciting opportunity to make a significant impact in the industry.

Qualifications

• 3+ years of experience in Regulatory Affairs required.
• Knowledge of EMA and European drug development regulations.

Responsibilities

• Manage regulatory submissions and timelines for clinical studies.
• Collaborate with cross-functional teams for regulatory document planning.

Skills

Regulatory Affairs

Clinical Trial Applications (CTAs)

EMA Regulations

Interpersonal Skills

MS Office Suite

Education

BA/BS in Biological or Health Sciences

Master’s, PhD or PharmD

Tools

Electronic Document Management Systems

Document Review Tools

Job description

Job Title: Senior Manager, Regulatory Affairs

Department: Regulatory Affairs

Location: Oxford, UK

*Position will be on-site. Relocation support will be considered for this role.

Overview of Role:

Reporting to European Regulatory Director, the Senior Manager of Regulatory Affairs will support the day-to-day regulatory activities of assigned projects. These assigned projects include support of preparation and compilation of submissions for regulatory agencies, tasked clinical studies, management of regulatory submission processes and timelines, regulatory tracking tools, archives, and infrastructure, as assigned.

The role is primarily home based out of: UK, Ireland, Germany, Belgium, Netherlands, Switzerland

Role and Responsibilities:

• Provide ownership of projects and activities, including clinical trial applications (CTAs) and other European focused MAA pre-submission activities.
• Contribute and drive the regulatory content and strategy for marketing authorization submissions and pre-MAA submissions
• Provide regulatory guidance internally on study-team decisions
• Update study/project teams of regulatory activities in the context of study team management meetings
• Manage and track queries, commitments and submissions with reference to regulatory agencies, collaborate with subject matter experts to provide responses as necessary, provide periodic status updates regarding unfulfilled conditions/commitments
• Collaborate with cross-functional study team for planning of regulatory documents, including health authority meetings such as scientific advice, paediatric and/or orphan designation.
• Contribute to, or lead, internal meetings such as kick off meetings, cross functional project updates
• Manage/Support internal document processes, including reviewed, finalized, signed-off, and archiving
• General support of global / other region regulatory submissions and strategic planning as applicable
• Contribute to / and track regulatory compliance pre and post approval
• All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:

• BA/BS degree in the biological or health related sciences required, Master’s, PhD or PharmD preferred
• Minimum 3+ years of experience in Regulatory Affairs
• Minimum 7+ years of pharmaceutical, biotechnology or life science industry experience
• Knowledgeable of EMA and European guidance’s, regulations, drug development process, and industry-standard practices
• Possess strong written, oral communications
• Demonstrate proven interpersonal skills and experience working cross-functionally throughout the organization
• Detail-oriented, ability to work proactively, organize, prioritize, and delegate assigned projects
• Experience interacting with CROs e.g. CTAs, Clinical trial activations experience preferred
• Experience of EU/European health authority systems such as IRIS, CTIS is desirable
• Proficient user of standard MS Office suite (e.g., Word, Powerpoint, Excel), experience using electronic document management systems, and document review tools desirable

Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s human resources department to obtain prior written authorization before referring any candidates to Summit.