Team Lead - Breda, United Kingdom - IMC LOCUMS LIMITED

IMC LOCUMS LIMITED

Verified Company

Breda, United Kingdom

1 week ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Seeking a highly motivated individual for the role of Team Lead and full-time Senior/Principal Consultant for a leading product development and regulatory affairs consultancy serving the pharmaceutical and biotechnology industry based in Breda, NL.

Our internationalteam offer strategic and operational support in the fields of CMC, nonclinical/toxicology, clinical/medical and regulatory, which guides products efficiently from early development stages to marketing approval.

You
must have full right to work and reside in the EUas sponsorship cannot be provided for this role.

This role
offers Hybrid working arrangements and the expectation is you will be in the office a minimum of 2 days per week.

This role
involves line management responsibilities
We are looking for an ambitious individual with excellent team management and communication skills.

You will form part of our operational leadership team, playing a pivotal role in supporting the evolution and expansion of our Netherlands Office, in collaborationwith the Technical Head, NL.

Key Objectives

Act as Team Lead for the Netherlands office, providing leadership and guidance to the country team, with appropriate escalation to the Head of Project Management, Deputy Head of Project Management, Head of Resourcing and COO for operational issues
Serve as a point of escalation for the local team, providing timely, accurate feedback and support
Fulfil the role and responsibility of Prevention Officer regarding H&S and ensure that the project team adhere to our processes and procedures
Provide strategic, technical, and regulatory advice/services to clients in all areas of the development of human medicinal products
Lead multijurisdiction programs of work and deliver consulting services within your respective area of expertise
Review written estimates, quotations and contracts for Clients as required
Ensure delivery of project goals within agreed client/team timelines, maintaining oversight of project budgets
Generate additional business from current Clients through exceeding expectations relating to the quality, delivery time and cost of services, and empower others to do the same
Educate clients on current regulatory trends and expectations. Where relevant, champion the client's view for development of products with other contractors such as CROs
Establish and maintain a high level of technical knowledge in the area of product development and international regulatory affairs
Support the development and operation of the alliance network and new partnership opportunities
Challenge the regulatory 'statusquo' from a technical and scientific standpoint
Represent our clients in regulatory agency interactions and provide regulatory solutions to agency objections
Lead meetings with internal and external stakeholders on matters related to any current and/or future projects, contracts, or new business opportunities
Provide strategic input/support to our Directors and the company's growth plan
Line manage individual contributors, and in so doing provide ongoing coaching and mentoring
Mentor and train junior members of the consultancy team (including Consultant and Associate levels)
Represent us at seminars, conferences, and events

About You

A minimum of 5 years of employmentrelated experience in regulatory and 10 years' experience in a pharmaceutical or service provider Industry role
Proven team leadership abilities
A professional manner and presentable appearance for meeting customers/clients
Ability to work in a proactive and autonomous manner as well as leading a team
Ability to balance competing priorities and complete work within a set timeframe
Exemplary organisational skills with a high level of attention to detail
Exemplary verbal communication and presentation skills in English
High level of computer literacy and competency in MS Office programs
Willingness to work flexible hours and travel for short periods, sometimes at short notice, within the Netherlands, Europe, the UK or internationally
RAC/TOPRA accreditation is an advantage

Benefits

A competitive salary, which is commensurate with experience
Generous annual bonus program, which rewards success
26 days' vacation plus discretionary additional days for birthday and work anniversary and public holidays
5% Employer pension contribution
Compensation of Private Healthcare insurance
Access to Employee Assistance Programme
Employee Ownership Trust Scheme
An opportunity to influence global business strategy, and associated implementation