Its not often that I see a company with such a good pipeline and position offer candidates the option to work hybrid.
If you are looking to grow your career, increase your flexibility, work for an upcoming biotech or all three - then please continue reading and get in touch.
(and of course, if you do want to work in the office, relocation is supported)
As a Clinical Development expert you will be responsible for;
*Significant work with all Development Drug Phases ( I-III ) with a focus in delivering Clinical Strategy, Team Leadership, patient safety, trial design etc.
*Support the Stop-Go decision making process with the Chief Medical Officer and determining the most effective use of Key Targets, Molecules, Budget etc.
*Strong organizational, communication, negotiation and interpersonal skills. Ability to effectively influence upper management, affiliates, regulatory agencies, and industry to ensure that regulatory and business needs are met. Understanding of the concept and application of Good Clinical Practices and clinical design.
*Responsible for budget maintenance and allocating funds according to research results, strategy and company decisions.
*Work with regulatory bodies (FDA/EMA) to bring drugs further into filling and submission.
*Manage a team of Clinical Scientists, Medical Professionals and other related functions - inspiring them and supporting them on their own career development.
*Guide, consult and ensure Clinical Development Standard Operating Procedures (SOPs) are effective and align with the strategy you create.
*Act as a Key driver to multiple programmes, supporting internal colleagues with your experience and helping external stakeholders with your in-depth product, scientific and medical knowledge of the pipeline.
As a clinical development project lead you will need;
*M.D or equivalent (Board Certification is not required but strong Onco/Haem experience within the industry is desirable).
*Previous work within oncology- either in Solid or Haematological mainly in the industry (Biotech, Pharma or CRO).
*Strong Clinical Development experiences, ideally both in Pharma and Biotech but either is fine.
*Track record of working globally.
*Excellent stakeholder management, internally and externally - good communication will be key.
*Fluent in English.
*Enjoys fast moving, highly scientific working environments and not afraid to help other colleagues or departments when needed.
Package:
*Salary to be discussed.
*UK (and Non-EU) Applications welcomed.
*Vacation days.
*Group pension plan.
*Continued career support
*Housing and child support if needed
*Working with some of the most newest oncology treatments in Europe
*Being lead in an open work culture and under the leadership of 3 highly respected oncologists and industry veterans.
If you are interested in this mission, or in general would like to discuss your options in the Clinical Development space then please send your CV in, apply on LinkedIn or contact me.
tihana.sujica@epmscientific.com
This will be confidential and your CV will not be shared to anyone without your permission.
Please apply now as this role will fill very quickly
