Senior Consultant & Team Lead

Job title:

Senior Consultant & Team Lead

Company:

Barrington James

Job description

Job DescriptionSenior Consultant & Team LeadLocation: NetherlandsEmployment Type: Full-TimeOverviewAn opportunity has opened for a motivated professional to take on a Senior Consultant & Team Lead role within a dynamic and fast-growing regulatory consultancy. Based in the Netherlands, the position offers a hybrid work environment, requiring a minimum of two days per week in the office. This role is ideal for an experienced regulatory professional eager to lead a high-performing team and provide strategic, technical, and regulatory expertise to a wide variety of clients.Responsibilities

• Lead and manage the Netherlands operational team, ensuring smooth integration and alignment with the broader global organization.
• Act as the key liaison for the Netherlands team, providing updates, feedback, and escalations to the global operations leadership.
• Provide mentorship and technical guidance to junior team members in collaboration with the Technical Head for the Netherlands.
• Deliver strategic regulatory consulting services, including innovative drug development plans, regulatory strategies, and data gap analyses.
• Author and review critical regulatory documents such as clinical trial applications, scientific advice briefing packages, orphan drug applications, and marketing authorization submissions.
• Oversee and manage multi-jurisdictional projects, ensuring delivery within agreed timelines and budget parameters.
• Represent clients in regulatory interactions, providing solutions to address agency feedback or objections.
• Lead internal and external stakeholder meetings related to ongoing projects or business development opportunities.
• Play an active role in business development by generating additional opportunities with current and new clients.
• Fulfill health and safety responsibilities at the Netherlands location and contribute to the operational development of the local office.

Qualifications and Experience

• A life sciences-focused BSc and an advanced degree (MSc or PhD preferred) in a biomedical field. A strong background in toxicology is essential.
• A minimum of 8-10 years of drug development experience, with direct involvement in regulatory negotiations with authorities such as EMA, FDA, or MHRA.
• Proven ability to create strategic regulatory plans for projects from early development through marketing authorization.
• Strong leadership skills, including team management and the delivery of internal training or external scientific presentations.
• Excellent organizational abilities with high attention to detail, capable of working proactively and independently.
• Proficiency in English, both written and verbal, and experience using MS Office tools.
• Flexibility to travel domestically or internationally on short notice.

Benefits

• Competitive salary with a generous performance-based bonus program.
• 26 days of vacation, with additional discretionary days for birthdays and work anniversaries.
• 5% employer pension contributions and private healthcare coverage.
• Access to employee wellness programs and ownership schemes.
• Opportunities for ongoing professional development through mentoring and training.

About the OrganizationThe company is a globally recognized consultancy specializing in product development and regulatory strategies. With teams spanning multiple countries, they are dedicated to delivering high-quality solutions that accelerate innovation in healthcare. Their inclusive and collaborative culture emphasizes sustainability, employee involvement, and a commitment to client success.#LI-OG1

Expected salary

Location

Nederland

Job date

Tue, 03 Dec 2024 23:46:05 GMT

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