Associate Principal Scientist Job Description
Associate Principal Scientist Duties & Responsibilities
To write an effective associate principal scientist job description, begin by listing detailed duties, responsibilities and expectations. We have included associate principal scientist job description templates that you can modify and use.
Sample responsibilities for this position include:
Associate Principal Scientist Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Associate Principal Scientist
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Education for Associate Principal Scientist
Typically a job would require a certain level of education.
Employers hiring for the associate principal scientist job most commonly would prefer for their future employee to have a relevant degree such as Master's and Bachelor's Degree in Chemistry, Biochemistry, Science, Engineering, Chemical Engineering, Biology, Microbiology, Biological Sciences, Pharmaceutical Sciences, Life Sciences
Skills for Associate Principal Scientist
Desired skills for associate principal scientist include:
Desired experience for associate principal scientist includes:
Associate Principal Scientist Examples
Associate Principal Scientist Job Description
- Candidate will work as member of a multidisciplinary team to solve complex technical problems related to production of biotherapeutics
- Lead interactions with end-users to understand business needs and develop solutions based on Advanced Process Control principles
- Active engagement with IT groups to implement solutions
- Conceptualize, design and develop biochemical and biophysical assays for high throughput screening and follow up characterization of hit classes of interest
- Responsible for the design, execution and delivery of formulation and process development studies for liquid and lyophilized parenteral drug products of biologics
- Critically review and interpret raw data and information
- Ensure documentation of work
- Interface with scientists and physicians in early and late stage clinical development to execute on biomarker strategies in clinical trials
- Serve as a subject matter expert in tissue-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials
- Develop mass spec methods to characterize nucleic acids, proteins, lipids, and other biomolecules
- Experience in applying innovative tools such as Systems Biology
- A strong track record of achievement and experience of working on programs aimed at identifying novel treatments for neurodegenerative diseases
- An international reputation for research excellence and can show evidence of research productivity
- Advanced computer skills using MS Office Suite (Outlook, Word, Excel, Power Point )
- Bachelor's degree in Bio-Engineering, bio-related Science Discipline
- A minimum of 3 years of industry experience in drug discovery
Associate Principal Scientist Job Description
- Technical project leadership and lab contributions, spanning multiple initiatives in small-molecule and synthetic polymer delivery materials development and manufacturing
- Act as a link between projects and venture/partner programs in the provision of materials
- Managing in a cross-functional matrix of scientists and engineers internally and external to Moderna
- Contribution to strategy and execution of maintaining supply of novel delivery materials
- Communicate progress, challenges and findings regularly to inform program development stakeholders
- Establish and perform in vitro human based immune cell tumor cell co-culture systems tumor explant systems to enable the pharmacological characterization of drug candidates for cancer immunotherapy
- Contribute to scientific projects to discover innovative immune-cell targeting drugs for cancer immunotherapy
- Collaborate and coordinate effectively with external collaborators other research teams and disciplines across a global discovery research organization
- Propose novel targets and design experiments for target ID and validation
- Lead early discovery projects
- 3 years of drug discovery experience in industry
- The position requires either a BS and/or MS in Chemical Engineering or related field from an accredited college/university plus at least 8 years of relevant work experience in process development, or a PhD in Chemical Engineering or a related field from an accredited college/university with at least 3 years of relevant experience
- Biomedical sciences and genetics/genomics
- Bioinformatics / computational biology / machine learning
- Career experience in human disease research and therapy
- Experience in scientific leadership, mentorship and teaching
Associate Principal Scientist Job Description
- Conduct experiments and generate data
- Present results to project team and senior management
- Application of informatics and modeling techniques to accelerate the evolution of drug discovery leads to drug candidates
- Collaboration with discovery teams to invent novel medicines including contributing to project strategy
- Provide technical/team support and leadership (matrix, project) in manufacturing sciences for late stage cell culture process development, scale-down model development/execution/implementation, process characterization, commercial technology transfer, and qualification studies associated with the development and implementation of bulk processes, systems and facilities related to biologics products.
- Support definition and development of process control strategy including identification of critical process parameters and critical material attributes for upstream process and raw materials (including media/feed components)
- Partnering with commercial manufacturing teams to provide post approval support and upstream subject matter expertise support to ongoing manufacturing activities
- Supporting evaluation and development of innovative process technologies, continuous process improvements and post commercial process enhancements (including development of next generation processes post approval) to support in-line products
- Application of science and risk-based approaches to the characterization and qualification of raw materials (including complex media and nutrient feed components) for the biologics manufacturing
- Collaborate with internal/external partners (Raw material suppliers, external manufacturers )
- Well networked across bioinformatics and scientific communities
- Demonstrated ability to form productive collaborative relationships
- A proven track record delivering impactful scientific insight from sequencing and multi-omic data through technical advances in bioinformatics analysis and pattern discovery
- Experience in developing HACCP/Food Safety Plans and preventive control programs
- Vaccine clinical development experience
- PhD or equivalent degree in statistics/biostatistics or related discipline, or a Master’s degree with a minimum of 3 years relevant experience
Associate Principal Scientist Job Description
- Lead cross functional teams and ensure alignment with analytical strategies and Quality Systems in support of late-stage activities (Phase III clinical trials, launch, life-cycle management) for novel vaccines and biologics
- Develop and optimize biochemical, immunochemical and chromatography-based analytical methods (in lab)
- Prepare and execute analytical method transfers and assay method validations, including authoring and coordinating review of protocols and reports
- Provide on-going support to internal staff and external partners to resolve analytical issues and trouble-shooting
- Coordinate analytical issue resolution via subject matter experts within the global vaccines and biologics networks (as needed)
- Contribute as author and reviewer to regulatory submissions
- Independently create and drive execution of regulatory strategy to support lifecycle management of In-line
- Lead, collaborate and communicate with Country Regulatory Leads, Regional Leads, Regional Liaisons, other functional areas within Global Regulatory Affairs and Clinical Safety, MRL and across Divisions with GHH and MMD to ensure alignment around a common set of priorities and objectives for ROW filings and lifecycle management activities
- Align with cross functional team to help set the cocoa crop science agenda which will best support the Cocoa Life plan
- Work with internal and external scientists and operational teams to define complex technical challenges to be solved and determine the need for projects to address these
- Ability to collaborate with scientists and work on multi-discipline teams
- Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
- Experience in all phases of the drug discovery path up to recommendation for preclinical toxicology and clinical study
- PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 3 years relevant experience, or a Master’s degree with a minimum of 6 years relevant experience
- Demonstrated competency to develop project objectives aligned with business goals (consumer problem to solve, customer problem to solve, business problem to solve)
- Experience with a scientific programming environment
Associate Principal Scientist Job Description
- Translate academic research into farmer applicable recommendations
- Communicate outputs from the projects both to the senior RDQI teams and the Cocoa life team to ensure that the learning is embedded in the business to maximize the benefit to the farming community and the business deliverables
- Research and keep up-to-date with developments in cocoa crop science and crop science in general
- Supervise research projects to develop cocoa crop science, both internally and externally
- Maintain and develop cocoa growing resources including data management systems and library, working with IT department to maintain security and back-up systems
- Other RDQ support as required
- Lead the design, planning and execution of multi-step organic synthesis of novel components for our lipid nanoparticles to solve delivery challenges for multiple therapy areas
- Manage a team of associate chemists and ensure timeline adherence and project alignment to meet group and company goals
- Work within cross-functional teams to evaluate and optimize the efficiency and safety of our delivery technologies for multiple therapy areas
- Collaborate on the development of novel in vitro assays for the characterization of lipid nanoparticles and their components
- Experience working for or with an imaging CRO for late stage clinical trials (ie
- The candidate should have working knowledge of industry guidelines
- Bachelor's degree in Pharmaceutics, Chemical Engineering or related-field with a minimum of 8+ years of experience
- Advanced experience in quantitation of multiple analytes
- Ability to multi-task in a highly dynamic environment and flexibility to work in a fast-paced team in a professional and pleasant manner is a necessity
- History of publication in peer-reviewed journals