Sr Scientist – Bioanalytics , client dedicated

Job title:

Sr Scientist – Bioanalytics , client dedicated

Company:

Thermo Fisher Scientific

Job description

Work Schedule Standard (Mon-Fri)Environmental Conditions OfficeJob DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefitsWe are actively looking for a highly motivated Senior Scientist Bioanalytics with extensive expertise in clinical drug development of large molecules.The candidate will serve as the bioanalytical lead for a biological compound, represent the bioanalytical team in one or multiple project teams, and closely collaborate with internal and external partners. The Senior Scientist will be responsible for designing and implementing bioanalytical assay strategies for the assigned projects.Ideally this role would be based at our client site in Ghent, Belgium.Remote work can be discussed, provided the candidate is able to be present in the Ghent office several times per month for multiple days.Responsibilities

• Responsible for the development and implementation of the bioanalytical strategy by working closely with cross-functional team members and acting as a key member of project/indication teams.
• As a bioanalytical expert, responsible for developing assay validation strategies that comply with regulatory guidelines and industry best practices.
• In collaboration with the sourcing manager and program manager, oversee the timely commissioning of validation packages and the bioanalysis of clinical trials by bioanalytical vendors. Participate in vendor governance meetings, as appropriate.
• As a bioanalytical study monitor, responsible for the oversight of bioanalytical study phases of clinical trials, including the review of sample analysis plans and reports, and for providing input into clinical trial documents (e.g., clinical study protocols, data transfer agreements, lab manuals, etc.).
• Participate in project team meetings as a recognized bioanalytical expert.
• Collaborate with medical writers in drafting the bioanalytical modules in regulatory documents.
• Contribute to interactions with regulatory agencies.
• Stay current with relevant literature, maintaining awareness of scientific and bioanalytical developments and how they may apply to argenx clinical development programs.
• Present results and findings at internal multidisciplinary project, clinical, and bioanalytical team meetings.

Required Education and Experience:

• PhD degree or equivalent experience.
• At least 5 years of industry experience in the field of bioanalytical sciences.
• Hands-on experience with ligand binding assay methods and platforms; experience with LC-MS technology for large molecules is a plus.
• Experience in analyzing human samples in support of clinical trials, with a solid understanding of GCP/GCLP guidelines and other current global regulations.
• Experience in the development and validation of PK, PD, and immunogenicity assays for large molecules, including knowledge of the respective regulatory guidelines.
• Experience running outsourced activities.

BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Expected salary

Location

Bruxelles

Job date

Thu, 14 Nov 2024 23:31:00 GMT

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