Senior Regulatory Affairs Specialist

We are currently seeking a Senior Regulatory Affairs Specialist to join our global Regulatory Affairs department. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and...

**Careers that Change Lives **In this exciting role as an Associate Regulatory Affairs Specialist, you will be in charge to prepare Regulatory Affairs (RA) meetings (regulatory status) involving cross-functional business partners under your responsibility. To provide status on time about projects and all applicable regulatory activities assigned by Senior...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description**: The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance,...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client...

**Work mode**: **Onsite Location(s)**:Lima, LIM, PE **Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** - At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office We are currently seeking a Principal Regulatory Affairs Specialist to join our global Regulatory Affairs department. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. In this role you will be a pivotal team...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client...

Tether Operations LimitedPEN 70,000 - 100,000 (estimated)Company Overview: Tether is a pioneering company in the stablecoin and blockchain industry, committed to pushing the boundaries of innovation and technology.About the Role: We are seeking an experienced Regulatory Affairs Strategist to design and execute global regulatory strategies for our biotech...

The career you're looking for starts here. Find the role that will give you challenges and opportunities. If you are one of our employees who is interested in a job advertised on this website, then we encourage you to find out more and apply here. Communication and External Affairs Specialist At First Quantum, we free the talent of our people by taking a...

At Thermo Fisher Scientific, we offer a competitive remuneration package, including an annual incentive plan bonus, healthcare benefits, and a range of employee perks. Our innovative organization is built on a foundation of integrity, intensity, involvement, and innovation.We are seeking a skilled Regulatory Compliance Specialist to join our team. This role...

At First Quantum, we free the talent of our people by taking a very different approach which is underpinned by a very different, very definite culture – the “First Quantum Way”. Working with us is not like working anywhere else, which is why we recruit people who will take a bolder, smarter approach to spot opportunities, solve problems and deliver...

Communication and External Affairs Specialist At First Quantum, we free the talent of our people by taking a very different approach which is underpinned by a very different, very definite culture – the “First Quantum Way”. Working with us is not like working anywhere else, which is why we recruit people who will take a bolder, smarter approach to...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies and projects. You will be part of a global team providing innovative...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring...

Job Summary - This is a Senior Manager position who will lead, manage and provide strategic direction to the country regulatory team. - Accountable for all strategic regulatory activities for the country including pre - and post-authorization product lifecycle activities and delivery of operational regulatory activities in partnership with above-country...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The following skills are required to be successful in this position: - preparation and assembly of global regulatory submissions - interacting with sponsors, - review and assess clinical trial regulatory documents, - review and assess scientific literature. - manages project teams...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Essential Functions and Other Job Information**: - Supports the preparation of documentation and submissions of North American IRB and REB submissions - Coordinates and manages client deliverables supporting regulatory compliance. - Liaises with internal and external clients in...

Essential Functions and Other Job Information: - Supports the preparation of documentation and submissions of North American IRB and REB submissions. - Coordinates and manages client deliverables supporting regulatory compliance. - Liaises with internal and external clients in the tracking and status update of project plans and overall support of...