Sr Regulatory Specialist
About the role
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Senior Regulatory Specialist
Location: Flexible location in Barcelona, Munich, London, Rome and Lyon
ICON are currently looking for a Senior Regulatory Specialist to join our Real World Evidence team. Working within our Real World Evidence team, you will work with a team of professionals who provide strategic and operational expertise in the design and conduct of Post-Approval and commercialization programs for Pharmaceuticals, Biologics and Medical Devices.
Combining the industry’s oldest and most experienced Clinical Outcome Assessments (COA) consultancies (Mapi & Oxford Outcomes), within ICON Commercialisation and Outcomes, and with access to more combined COA experience than all other CROs and consultancies, we can offer fantastic career opportunities. We provide a dynamic, stimulating and rewarding working environment for ambitious and passionate individuals looking to join a global, world-class consultancy business.
Your Responsibilities and Accountabilities:
The Senior Regulatory Specialist works closely with the site contracts and ethics and regulatory teams in providing support in managing all regulatory aspects of the assigned projects in accordance with protocol specifications, applicable guidelines, regulatory requirements and SOPS.
Responsibilities:
In the role of Senior Regulatory Specialist, you will be:
- Responsible for oversight of regulatory submissions for assigned projects/countries/sites, which may include completion of submissions or notifications, as required.
- Responsible for providing advice and support to the project team for regulatory aspects of the projects.
- Responsible for providing regulatory support as needed for drafting applicable study documents, including the protocol and informed consent form.
- Responsible for investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
- Responsible for providing input and oversight for ongoing development and enhancement of systems used in the frame of Regulatory Affairs activities.
- Responsible for updating and maintaining regulatory information in the Study Management System and/or reporting mechanism, and for ensuring appropriate paper and electronic filing.
- Responsible for liaising with other departments on requirements for regulatory submissions.
- May act as a Contract Specialist if appropriately trained.
- Participating in the improvement of the Quality Assurance System.
- Coaching and mentoring more junior memebers of the team
You will have:
- Education to degree level
- Strong knowledge of ICH/GCP guidelines or other relevant guidelines (GEP, GPP or local requirements)
- Proficiency with computer systems
- Strong verbal and written communication skills
- Strong organisational, time management, interpersonal skills.
- Ability to work both independently and in a team environment.
- Some team coaching / mentoring experience
This is a great global role for someone with a solid grounding in these subjects and tasks but may need to learn some element eg site contracts knowledge.
Next Steps:
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
ICON Plc is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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Application process
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Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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