Db Pension Consultant
2 weeks ago
Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. Scendea’s international team offers strategic and operational support in the fields of CMC, nonclinical/toxicology, clinical/medical and regulatory, which guide products efficiently from early development to marketing approval.
With a current team of over 50 staff based in the UK, Australia, the Netherlands, and the US, Scendea is undergoing a period of significant growth, with the addition of new office locations and service lines to facilitate the delivery of expert and strategic global regulatory consulting services to its rapidly growing client base.
Scendea is seeking a technical clinical strategy expert to join our team as a full-time Principal Consultant (Clinical). It is important that the candidate has established experience in working independently and leading technical discussions on a range of clinical development topics in compliance with current regulatory requirements. They will need to be competent in direct hands-on clinical writing and review of documents for regulatory submissions.
This is an excellent opportunity to progress your career at a rapidly growing Regulatory Consultancy. You will have the opportunity to play a key role in the development and mentoring of staff whilst providing high-quality regulatory technical advice and product development strategies for clients.
Provide strategic, technical, and regulatory advice/services to clients in the area of clinical development of human medicinal products, across a wide range of therapeutic indications
Offer support and advice across a broad range of regulatory activities
Provide innovative drug development plans, data gap analyses and international regulatory strategies from a Clinical perspective for complex products within the changing regulatory environment
Support Scendea's Business Development in sales/marketing introductions, preparation of project proposals & educational materials, review written estimates, quotations and contracts for Clients as required
Contribute to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applications, Protocols, Investigator Brochures, IMPDs, CSRs, Marketing Authorisation Applications, New Drug Applications, Biologic License Applications, according to area of expertise
Provide technical leadership to other members of the Scendea consultancy team, including other Principal and Senior Consultants
Lead multi-jurisdiction programs of work and deliver consulting services within your respective area of expertise
Represent Scendea clients in regulatory agency interactions and provide regulatory solutions to agency objections
Ensure delivery of project goals within agreed 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 ‘status quo’ from a technical and scientific standpoint
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 Scendea Directors and the company's growth plan
Line manage individual contributors, and in doing so, provide ongoing coaching and mentoring
Mentoring and training junior members of the Scendea consultancy team (including Senior Consultant, Consultant and Associate levels)
The role will be affiliated to our UK office in Bishop’s Stortford
The role will be flexible, working from home with a minimum of one office-based day per month
A high scientific calibre with a life science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life science focused MSc or preferably a PhD)
At least fifteen years of drug development experience, with at least five years in the area of biotechnology and regulatory affairs
Proven ability in defining and delivering creative scientifically driven solutions to technical development and regulatory issues
Preference for candidates who have direct experience in providing strategic regulatory planning for the delivery of industry development goals, up to marketing authorisation
Experience in negotiation with multinational regulatory authorities including, as a minimum, European, UK and US authorities.
Proven ability to deliver education via scientific conference presentations in chosen field and training of subordinates
Ability to work in a proactive and autonomous manner as well as leading a global team, to ensure high-quality of deliverables
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, UK or internationally, with travel to the UK office, Bishop’s Stortford on at least a quarterly basis
The leadership team continue to be dedicated to developing a great company culture through initiatives such as the Scendea Academy, Values Engagement and Internal Community Knowledge Creation of which the successful candidate will play a key role.
A competitive salary, which is commensurate with experience
~ Generous bonus program, which rewards success
~26 days Holiday plus Birthday and Work Anniversary
~5% employer pension contribution
~ Private Healthcare insurance
~ Access to Employee Assistance Programme
~ An opportunity to influence global business strategy, and associated implementation
~ A challenging and stimulating position for a dynamic and competent regulatory professional, who wishes to contribute to a growing business and a rapidly expanding team
~ Coaching and mentoring to support your continuous development
~ You are a motivated individual who can instil trust and confidence in our customer relationships whilst having a natural aptitude for getting the best out of people internally.
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