Explore career opportunities at Eli Lilly, a global healthcare leader committed to discovering and delivering innovative medicines. Eli Lilly is dedicated to improving the lives of people around the world by creating groundbreaking treatments for various diseases. Job seekers can find roles in 42 Eli Lilly jobs in the United States
PhD position – Drug Development
Posted 3 days ago
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"Knowledge becomes health" - we are filling this motto with life every day, developing new ideas and improv-ing old-established knowledge. The University Hospital Frankfurt has existed since 1914. Our around 8,500 employees contribute with their skills and knowledge to the 33 specialist clinics, theoretical clinical institutes, and administrative departments. The close connection of health care with research and teaching, as well as a climate of collegiality, internationality, and cross-professional cooperation characterize the university hospital.
PhD position – Drug Development(We are targeting applicants of all genders)
Part Time | limited up to 1 year | Announcement number:
We are seeking a highly motivated PhD student to join our teams at the Oellerich lab at the Department of Medicine 2 , Universitätsmedizin Frankfurt and the Knapp lab at Goethe University , starting from the earliest possible date. The Department of Medicine 2, Hematology and Oncology at the Goethe University Hospital Frankfurt offers the entire spectrum of cancer diagnostics and therapy as well as a research program focusing on several cancer entities. The laboratory of Prof. Stefan Knapp is part of the Institute of Pharma-ceutical Chemistry of the Department of Biochemistry, Chemistry and Pharmacy of the Goethe University Frankfurt am Main as well as the site head of the Structural Genomics consortium (SGC) in Frankfurt. The group is particularly interested in understanding structural mechanisms that regulate cellular signaling and in the development and rational design of selective inhibitors, so-called chemical probes, especially in the field of epigenetics, phosphoryla-tion-dependent signaling pathways, and the development of PROTAC. The two research laboratories are part of the Frankfurt Cancer Institute ( focusing on oncogenic signaling and therapy resistance mechanisms in lymphoma and acute myeloid leukemia ( and development of new therapeutic ap-proaches to advance them to the development of new drugs. ( respec-tively. The labs are also funded by the German Cancer Consortium (DKTK), which was founded in 2012 as one of the six German Centers of Excellence for Health Research (DZG) to promote the clinical translation of medical inno-vations. The DKTK brings together more than 20 academic research institutions and university hospitals at seven partner sites cooperate with each other and the German Cancer Research Center (DKFZ) in Heidelberg as the core center ( Translational projects are part of the German Cancer Aid (Krebshilfe) Network TACTIC that is coordinated by the Knapp Group allowing access to assay platforms for the development of pre-clinical small molecules.
- The key goal of the research project is to develop novel drugs and degrader molecules to target survival pathways in aggressive lymphomas (DLBCL). The project is based on our previous work discovering new drug target candidates that are highly relevant for DLBCL biology.
- Your primary responsibility will involve optimizing and developing the lead drug candidates, as well as contributing to structure-activity relationship studies in Prof. Knapp's lab. You will work in close collaboration with the Oellerich lab for the validation of the compounds and to study drug resistance mechanisms. You will work in an interdisciplinary environment. This project will cover a plethora of cutting-edge techniques from both collaboration partners including CRISPR/Cas9 screens and quantitative proteomics, protein biochemistry, structural biology and novel biochemical and biophysical and cell based screening methods.
- University degree (master or Staatsexamen) in pharmacy, biochemistry or a related discipline
- Enthusiasm and fascination for biomedical drug development in oncology
- High motivation for experimental lab work, data analysis, and presentation of data
- Experience in protein biochemistry, basic cell biological methods and assay development
- As this is a highly collaborative research project, the ability to work in a team, a sense of responsibility and proactivity are essential
- Beneficial:
- German, B1
- Previous experience in drug development
- Previous experience in cell culture or assay development
- Due to legal regulations, valid proof of measles immunity / measles vaccination is required.
- Collective agreement: In addition to an attractive salary based on a collective agreement with an annual special payment, you benefit from long-term security through company pension schemes
- Mobility: Free public transport in all Hessen (Free State Ticket Hessen)
- Campus: Our attractive university hospital campus offers a modern cafeteria, various cafes, and opportunities to rest in numerous green spaces. A walk on the riverside of the Main offers relaxation during breaks
- Work-Life-Balance: Part-time employment is possible, we offer childcare in our daycare center (if you have any questions, please contact UKF-Familienservice), child care during holidays
- Health Promotion: Benefit from our attractive health offers. We offer regular online and face-to-face courses on nutrition, relaxation, sports and exercise.
- Professional development: Internal and external training for your professional development
- Any questions? Many answers can be found in ourFAQs for new employees. If you have any further questions, please do not hesitate to contact us.
- Working environment: International and cosmopolitan working environment. Funding secured for at least 3 years with possible extension if needed. Full access to DKTK / FCI/GU and the Riedberg Campus facilities and education programs.
- Collaboration: Based on the vibrant research environment in Frankfurt, the project will interact with numerous national and international collaboration partners e.g. the National Cancer Institute (Louis Staudt, Bethesda, USA) and consortia such as TACTIC, TheraNova, the Structural Genomics Consortium and the SFB1530.
- Publications: Internationally competitive lab with publications in high-impact peer-review journals such as:
- Mohr, Cancer Cell, 2017
- Phelan, Nature, 2018
- Li et al., Science. 2024 Feb 2; ):498-503 (doi: /science.adm8095)
- Owens et al., Nat Chem Biol. 2024 Sep;20(9): . (doi: /s -0)
- Wilke et al. Blood 2022 (DOI: /blood. )
- Jayavelu et al. Cancer Cell 2022 (DOI: /j.ccell. )
- Scheich et al. Cancer Discovery 2023 (DOI: / .CD- )
- Phelan et al. Cancer Cell 2024 (DOI: /j.ccell. )
- Schwalm et al. Nature Comm 2024 (DOI: /s -5)
- Dopfer et al. Nature Comm 2024 (DOI: /s -5)
- Wu et al Nature Comm, 2019 (DOI: /s -2)
- Picaud et al Cancer Res 2015 (DOI: / .CAN- )
Women are underrepresented in these positions at the University Hospital Frankfurt. Applications from women are therefore particularly welcome. Disabled applicants are preferred if they have the same personal and professional qualifications.
Use the time until December 30, 2024 to apply. Please submit your online application including a possible starting date and your salary expectations. For further information regarding the position and project, please contact Dr. Niklas Dienstbier ( ).
#J-18808-LjbffrAssociate Research Scientist - Drug Development
Posted today
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InVitro Cell Research (ICR) is dedicated to solving some of the most difficult problems in aging and age-related disease, to extend human health span. We're looking for talented scientists to join our growing pre-clinical drug development team.
With us, you'll get to:
- Examine novel and existing therapeutics for their potential future use in humans, including conducting critical go/no-go experiments to inform development decision-making
- Collaborate with many other company teams
Please apply if you:
- Have a BS or MS in a biomedical field with 3-10 years of experience in pre-clinical drug development
- Have molecular/cellular biology and biochemistry experience
- Enjoy working in dynamic team environments
- Are passionate about finding drugs to help people live healthier and longer
- Even if you don't meet all of these criteria, please apply anyway
Ideally, you'll also have:
- A demonstrated record of research accomplishment in pre-clinical drug development bench work
- Experience with Luminex, flow cytometry, digital western blotting is preferred but not required
- Experience with Tecan robotic liquid handlers is also a plus
And you'll need:
- An easygoing, friendly personality
- The ability to work in the United States without sponsorship
Position title and compensation are commensurate with experience.
The compensation ranges listed below are starting ranges.
Starting base pay range: $60,000/yr - $00,000/yr
Starting bonus range: 3,000/yr - 10,000/yr
Senior Scientist, Machine Learning (Drug Development)
Posted 4 days ago
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Company Summary: Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro’s lead program is Alpha-1 Antitrypsin Deficiency (AATD). Korro is based in Cambridge, Massachusetts.
We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health.
Position Summary We are seeking an experienced and strategic Senior Scientist, Machine Learning to drive the development and application of machine learning solutions for genetic medicine discovery and development. This role offers the opportunity to apply deep learning and statistical methods in current and novel areas across our RNA editing platform, from target identification and oligonucleotide design to patient stratification and clinical optimization.
The ideal candidate will bring deep expertise in both machine learning and statistics, enabling rigorous experimental design, hypothesis testing, and model validation in complex biological systems. You will have significant autonomy to identify and explore new applications of ML/AI across diverse functions within the organization, working at the intersection of computational biology, drug discovery, and precision medicine.
Key Responsibilities- Drive research and development of novel deep learning architectures, training paradigms (e.g., supervised, self-supervised, generative, multi-modal), and algorithms tailored for large-scale biological sequence data and related modalities.
- Partner with computational biologists, data scientists, and data engineers to integrate domain expertise, define scientifically meaningful tasks, and apply cutting-edge machine learning research towards ambitious biological challenges.
- Design, implement, and maintain robust ML Operations (MLOps) pipelines for model training, evaluation, versioning, and deployment using cloud-based infrastructure and tools like AWS MLflow.
- Design and execute statistically rigorous experiments using design of experiments (DOE), A/B testing, and Bayesian approaches to optimize RNA editing strategies, validate model predictions, and advance our mechanistic understanding of RNA editing through testable biological hypotheses.
- Identify and prototype novel machine learning applications across diverse organizational functions including manufacturing optimization, supply chain analytics, regulatory strategy, and clinical trial design.
- Mentor early career scientists and engineers, fostering a culture of technical excellence and scientific curiosity through leadership and code review.
- Contribute to long-term strategic planning for ML/AI platform capabilities, identifying emerging technologies and research directions that could transform genetic medicine development timelines and outcomes.
- Share research findings through internal presentations and contribute to the scientific community via publications or presentations.
- PhD (or equivalent expertise) with a strongly distinguished research focus in Machine Learning, Computer Science, Statistics, Physics, or related quantitative field with 4+ years post-graduate experience in leading industrial R&D or highly competitive academic environments.
- Deep understanding of modern deep learning theory and practice, including Transformers, sequence models (e.g., state-space models), LLMs, and proven ability to implement, train, and debug high-performance models using PyTorch, JAX, TensorFlow, or R frameworks (torch, tensorflow/keras), with experience in associated libraries such as Flax, Equinox, PyTorch Geometric, or tidymodels.
- Proficiency in scientific computing and data analysis using R (tidyverse, Bioconductor, caret) and/or Python (pandas, numpy, scipy, scikit-learn) ecosystems.
- Experience working with large datasets and understanding the challenges associated with scale, including data preprocessing, feature engineering, distributed training, and cloud platforms (AWS/SageMaker, GCP, Databricks).
- Experience with graph neural networks, molecular representation learning, or willingness to rapidly acquire computational biology expertise.
- Track record of impactful research through publications in high-impact scientific journals with experience leading technical projects and mentoring junior researchers.
- Excellent communication skills, capable of discussing complex ideas with both domain experts and audiences with diverse backgrounds, and experience with ensemble methods, cross-validation, and model evaluation in production environments.
Korro offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking.
Seniority level- Mid-Senior level
- Full-time
- Other
Hematologist Oncologist - Director, Drug Development Unit TN
Posted today
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Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13636)
Posted today
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Overview
Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13636)
Location: Thousand Oaks, CA. 91320
Business Unit: Facilities & Engineering Substance Supply
Employment Type: Contract | Duration: 1+ year with likely extensions and/or conversion to a permanent position. Rate: $38 - $42/hour W2
Posting Date: 1/23/2025
Notes: Only qualified candidates need apply. Initial schedule M-F for the first month of training. Flexibility in schedule, role has potential to move to a Sun-Wed 4 day x 10 hour shift (estimate start time 8 am)
Job Description3 Key Consulting is hiring! We are recruiting an Engineer, Upstream Drug Development Facilities & Engineering for a consulting engagement with our direct client, a leading global biotechnology company.
Our Ideal Candidate: Works Onsite, is an expert in upstream drug substance, equipment ownership, specializing in cleaning systems like CIP, COP, Autoclaves, and Glass Washers. Has a strong foundation in engineering principles, excellent communicator.
Seeking an Engineer at our client’s main headquarters in Thousand Oaks, CA to join the GMP Facilities and Engineering (F&E) organization. This position will provide on-site engineering support for the B23 Drug Substance Plant.
Responsibilities- Under general supervision, provides equipment ownership by being SME of equipment. This position is to be the engineer for cleaning systems, which includes CIP (Clean In Place), COP (Clean Out of Place), Autoclaves and Glass Washers. Main function is to ensure equipment is running safely and reliably for production. Applies basic engineering principles to troubleshoot, design and implement system modifications, perform function tests for small projects. Organizes, analyzes and presents interpretation of results for engineering projects and/or issues of minor to medium scope and complexity. Support senior engineers for the implementation of complex projects.
- Function as a technical expert to equipment or systems.
- Perform the system owner role for assigned systems to ensure equipment safety, reliability and compliance.
- Work with manufacturing, maintenance, instrumentation, quality in order to resolve issues.
- Directing and coordinating equipment maintenance as necessary to ensure systems are in proper working order.
- Analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses.
- Specifying and overseeing a properly executed preventive maintenance program.
- Specifying proper spare parts for system.
- Basic Qualifications: M.S. or B.S. with 1+ years of experience in a GMP regulated environment; Troubleshooting or equipment ownership experience required.
- Top Must Have Skill Sets:
- Experience with regulated environments with working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech equipment.
- Direct experience with manufacturing process equipment including troubleshooting, reliability and performance improvements, and design optimization.
- Team player prepared to work in and embrace a team based culture that relies on collaboration for effective decision-making.
- Must be able to communicate clearly. Required to communicate out issues and updates to broader audience.
- Red Flags: No troubleshooting or equipment ownership experience.
Interview with 3 engineers possibly in 1 to 2 interviews. Can start interviewing ASAP.
We invite qualified candidates to send your resume to If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
#J-18808-LjbffrJob Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13348)
Posted today
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Job Description
Overview
Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13348)
Location: Thousand Oaks, CA. 91320
Business Unit: Facilities & Engineering Substance Supply
Employment Type: Contract
Duration: 1+ year with likely extensions and/or conversion to a permanent position.
Rate: $38 - $42/hour W2
Posting Date: 11/5/2024.
Notes: Only qualified candidates need apply. Initial schedule M-F for the first month of training. Flexibility in schedule, role has potential to move to a Sun-Wed 4 day x 10 hour shift (estimate start time 8 am)
3 Key Consulting is hiring! We are recruiting an Engineer, Upstream Drug Development Facilities & Engineering for a consulting engagement with our direct client, a leading global biotechnology company.
Overview of the RoleSeeking an Engineer at our client’s main headquarters in Thousand Oaks, CA to join the GMP Facilities and Engineering (F&E) organization. This position will provide on-site engineering support for the B23 Drug Substance Plant. Under general supervision, provides equipment ownership by being SME of equipment. This position is to be the engineer for cleaning systems, which includes CIP (Clean In Place), COP (Clean Out of Place), Autoclaves and Glass Washers. Main function is to ensure equipment is running safely and reliably for production. Applies basic engineering principles to troubleshoot, design and implement system modifications, perform function tests for small projects. Organizes, analyzes and presents interpretation of results for engineering projects and/or issues of minor to medium scope and complexity. Support senior engineers for the implementation of complex projects.
Responsibilities- Function as a technical expert to equipment or systems.
- Perform the system owner role for assigned systems to ensure equipment safety, reliability and compliance.
- Work with manufacturing, maintenance, instrumentation, quality in order to resolve issues.
- Direct and coordinate equipment maintenance as necessary to ensure systems are in proper working order.
- Analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses.
- Specify and oversee a properly executed preventive maintenance program.
- Specify proper spare parts for system.
- Equipment troubleshooting, improvement and reliability projects, ensuring that equipment work orders are completed on time.
- Experience with regulated environments with working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech equipment.
- Direct experience with manufacturing process equipment including troubleshooting, reliability and performance improvements, and design optimization.
- Team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
- Must be able to communicate clearly. Required to communicate issues and updates to a broader audience.
- M.S. with 1+ years of experience or B.S. with 2+ years in a GMP regulated environment. Troubleshooting or equipment ownership experience required.
Supplement to the team’s workload.
Interview Process- Interview with 3 engineers possibly in 1 to 2 interviews.
- Can start interviewing ASAP.
We invite qualified candidates to send your resume to If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
#J-18808-LjbffrJob Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13636)
Posted today
Job Viewed
Job Description
Overview
Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13636)
Location: Thousand Oaks, CA. 91320
Business Unit: Facilities & Engineering Substance Supply
Employment Type: Contract | Duration: 1+ year with likely extensions and/or conversion to a permanent position. Rate: $38 - $42/hour W2
Posting Date: 1/23/2025
Notes: Only qualified candidates need apply. Initial schedule M-F for the first month of training. Flexibility in schedule, role has potential to move to a Sun-Wed 4 day x 10 hour shift (estimate start time 8 am)
Job Description3 Key Consulting is hiring! We are recruiting an Engineer, Upstream Drug Development Facilities & Engineering for a consulting engagement with our direct client, a leading global biotechnology company.
Our Ideal Candidate: Works Onsite, is an expert in upstream drug substance, equipment ownership, specializing in cleaning systems like CIP, COP, Autoclaves, and Glass Washers. Has a strong foundation in engineering principles, excellent communicator.
Seeking an Engineer at our client’s main headquarters in Thousand Oaks, CA to join the GMP Facilities and Engineering (F&E) organization. This position will provide on-site engineering support for the B23 Drug Substance Plant.
Responsibilities- Under general supervision, provides equipment ownership by being SME of equipment. This position is to be the engineer for cleaning systems, which includes CIP (Clean In Place), COP (Clean Out of Place), Autoclaves and Glass Washers. Main function is to ensure equipment is running safely and reliably for production. Applies basic engineering principles to troubleshoot, design and implement system modifications, perform function tests for small projects. Organizes, analyzes and presents interpretation of results for engineering projects and/or issues of minor to medium scope and complexity. Support senior engineers for the implementation of complex projects.
- Function as a technical expert to equipment or systems.
- Perform the system owner role for assigned systems to ensure equipment safety, reliability and compliance.
- Work with manufacturing, maintenance, instrumentation, quality in order to resolve issues.
- Directing and coordinating equipment maintenance as necessary to ensure systems are in proper working order.
- Analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses.
- Specifying and overseeing a properly executed preventive maintenance program.
- Specifying proper spare parts for system.
- Basic Qualifications: M.S. or B.S. with 1+ years of experience in a GMP regulated environment; Troubleshooting or equipment ownership experience required.
- Top Must Have Skill Sets:
- Experience with regulated environments with working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech equipment.
- Direct experience with manufacturing process equipment including troubleshooting, reliability and performance improvements, and design optimization.
- Team player prepared to work in and embrace a team based culture that relies on collaboration for effective decision-making.
- Must be able to communicate clearly. Required to communicate out issues and updates to broader audience.
- Red Flags: No troubleshooting or equipment ownership experience.
Interview with 3 engineers possibly in 1 to 2 interviews. Can start interviewing ASAP.
We invite qualified candidates to send your resume to If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
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Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13348)
Posted today
Job Viewed
Job Description
Overview
Job Title: Engineer, Upstream Drug Development Facilities & Engineering (JP13348)
Location: Thousand Oaks, CA. 91320
Business Unit: Facilities & Engineering Substance Supply
Employment Type: Contract
Duration: 1+ year with likely extensions and/or conversion to a permanent position.
Rate: $38 - $42/hour W2
Posting Date: 11/5/2024.
Notes: Only qualified candidates need apply. Initial schedule M-F for the first month of training. Flexibility in schedule, role has potential to move to a Sun-Wed 4 day x 10 hour shift (estimate start time 8 am)
3 Key Consulting is hiring! We are recruiting an Engineer, Upstream Drug Development Facilities & Engineering for a consulting engagement with our direct client, a leading global biotechnology company.
Overview of the RoleSeeking an Engineer at our client’s main headquarters in Thousand Oaks, CA to join the GMP Facilities and Engineering (F&E) organization. This position will provide on-site engineering support for the B23 Drug Substance Plant. Under general supervision, provides equipment ownership by being SME of equipment. This position is to be the engineer for cleaning systems, which includes CIP (Clean In Place), COP (Clean Out of Place), Autoclaves and Glass Washers. Main function is to ensure equipment is running safely and reliably for production. Applies basic engineering principles to troubleshoot, design and implement system modifications, perform function tests for small projects. Organizes, analyzes and presents interpretation of results for engineering projects and/or issues of minor to medium scope and complexity. Support senior engineers for the implementation of complex projects.
Responsibilities- Function as a technical expert to equipment or systems.
- Perform the system owner role for assigned systems to ensure equipment safety, reliability and compliance.
- Work with manufacturing, maintenance, instrumentation, quality in order to resolve issues.
- Direct and coordinate equipment maintenance as necessary to ensure systems are in proper working order.
- Analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses.
- Specify and oversee a properly executed preventive maintenance program.
- Specify proper spare parts for system.
- Equipment troubleshooting, improvement and reliability projects, ensuring that equipment work orders are completed on time.
- Experience with regulated environments with working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech equipment.
- Direct experience with manufacturing process equipment including troubleshooting, reliability and performance improvements, and design optimization.
- Team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
- Must be able to communicate clearly. Required to communicate issues and updates to a broader audience.
- M.S. with 1+ years of experience or B.S. with 2+ years in a GMP regulated environment. Troubleshooting or equipment ownership experience required.
Supplement to the team’s workload.
Interview Process- Interview with 3 engineers possibly in 1 to 2 interviews.
- Can start interviewing ASAP.
We invite qualified candidates to send your resume to If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
#J-18808-LjbffrNurse - LPN or RN - Clinical Trials and Drug Development 9298
Posted 16 days ago
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Position: Nurse - LPN or RN - Clinical Trials and Drug Development 9298
Location: Madison WI
Schedule: Varies-rotating5:30AM-1PM6:30AM-3PM3PM-11PM11PM-7Am*Every Friday new schedule will be sent out for the following two weeks of shift schedule
Projected duration: 6 months + potential for perm
Job code: CVDJP
benefits are available
Job is at a clinical research facility
Preparing for upcoming studies, service healthy population of patients during clinical trial studies, dosing, watching for side effects to trials, administering trial doses, reporting and investigating side effects.
This would be the perfect fit for those looking to transition from hospital settings into nursing lab settings. Working with only healthy population of candidates during medical dosing trials.
Must be proficient with computers and electronic charting as Nurses are required to document trial doses and effects into computer systems
Senior Scientist - Drug Product Development
Posted 4 days ago
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Overview
Senior Scientist - Drug Product Development to join our client's innovative team in El Segundo, CA. This is a unique opportunity to lead protein formulation development efforts for biologic therapeutics in a cutting-edge biopharmaceutical environment. The ideal candidate is a creative and driven Scientist with deep expertise in biologics, drug product formulation, and protein formulation (mAbs).
RequirementsEl Segundo, CA (Onsite). Direct Hire | Biopharmaceuticals. $150,000 - $160,000/year (based on experience).
Responsibilities- Design and develop formulations for biologic drug products.
- Expertise in biologics, drug product formulation, and protein formulation (mAbs).
- Conduct hands-on laboratory experiments and coordinate with external testing partners.
- Collaborate cross-functionally with product development, process engineering, analytical development, and other engineering teams to advance drug development programs.
- PhD in Pharmaceutics, Biochemical Engineering, Chemical Engineering, Organic Chemistry, or a related field.
- Minimum of 5 years of industry experience in biologics production and protein formulation.
- Proven experience with regulatory submissions and addressing regulatory inquiries.
- Demonstrated success in biologics and protein formulation and development, supported by peer-reviewed publications and/or scientific presentations.
- Strong knowledge of biologic and protein formulation development across various dosage forms, including characterization and scale-up.
- Deep understanding of protein stability and product quality attributes.
We welcome you to be part of a large, historic global staffing company to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community for access to opportunities and this exclusive role. Benefits eligibility is in accordance with applicable laws and client requirements. Benefits include:
- Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
- Health Savings Account (HSA) (for employees working 20+ hours per week)
- Life & Disability Insurance (for employees working 20+ hours per week)
- MetLife Voluntary Benefits
- Employee Assistance Program (EAP)
- 401K Retirement Savings Plan
- Direct Deposit & weekly epayroll
- Referral Bonus Programs
- Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
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