Senior Researcher / Laboratory Leader Job at jobRxiv (Ostrava)

Senior Research Scientist (Pre-clinical) - 4DBio³ ODB

The Senior Research Scientist (Pre-clinical) serves as a scientific lead for pre...

Location

United States , Rockville

Salary:

135000.00 - 155000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Ph.D. in a relevant field (e.g., biology, pathology, biochemistry, bioengineering, molecular and cell biology, or genetics) required
3-5 years’ experience with planning and management of innovative medical and/or scientific research programs
Minimum 8 years direct experience in hematopoiesis research such as cell culture and differentiation of stem cells and/or synthetic blood substitutes
Experience with multi-color flow cytometry and cell sorting
Experience with blood cell function assays
Experience with gene editing and molecular biology techniques
Ability to design and execute in vitro experiments
Experience and success in writing and receiving federal research grants, cooperative agreements, and/or contracts
Experience working in DoD or other Federal research environments
Experience supervising research personnel

Job Responsibility

Perform recurring analyses on research portfolios to identify critical gaps, exceptional results and/or lack of progress
Assist in the preparation of SOPs and analysis of laboratory experiments
Prepare interim and final progress reports
Ensure research integrity
Disseminate research results
Provide guidance to scientists preparing research proposals, to include guidance on research protocol development, as needed
Maintain open communication with Principal Investigators and Center Leadership, advises of processes, reports progress, and serves as a point of contact, as applicable
Perform scientific reviews on research proposals submitted for consideration, as requested
Direct multifunctional teams and provides scientific domain expertise as needed
Adhere to Occupational Safety and Health Administration (OSHA), Good Laboratory Practices (GLP) and infection control procedures, as applicable

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year

Fulltime

Senior Scientist, Research

The Senior Scientist, Research, with limited guidance from more experienced scie...

Location

United States , Madison

Salary:

109000.00 - 185000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position
or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 4 years of related experience in lieu of a Ph.D.
or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 6 years of related experience in lieu of Ph.D.
3+ years of industry or academia experience in biology and/or chemistry
2+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
Demonstrated proficiency in molecular biology and/or biochemical techniques
Demonstrated proficiency in the principles of molecular biology, biochemistry, next-generation sequencing (NGS), genomics, and/or protein research
Working knowledge of statistical and mathematical methods in biology/genetics
including, but not limited to, statistical software, such as JMP
Strong understanding of GMP, ISO, and Quality Systems

Job Responsibility

Provide leadership to a team of junior research associates and scientists
Independently develop, plan, and conduct advanced research experiments, identify problems and discrepancies, analyze results, and identify and address trends in study data
Analyze research/experimental data, interpret the results, and provide insights into the next steps
Utilize and apply methods or technologies effectively and provide ideas for new techniques, when appropriate
Provide technical input and develop research plans, experimental outlines, and design
Prepare and provide information and data for scientific abstracts, industry conferences, project meetings, or publication
Generate, document, and communicate development plans for critical aspects of a project
Prepare and approve detailed technical procedures, protocols, and reports
Evaluate impact of nonconforming data to product or process
Maintain lab notebook in a clear, complete, and consistent manner, following all legal, ISO, and QSR requirements

What we offer

paid time off (including days for vacation, holidays, volunteering, and personal time)
paid leave for parents and caregivers
a retirement savings plan
wellness support
health benefits including medical, prescription drug, dental, and vision coverage
bonus eligible

Fulltime

Staff Scientist 2

Amentum is actively seeking applicants for Staff Scientist 2. The Staff Scientis...

Location

United States , Houston

Salary:

75000.00 USD / Year

Amentum

Expiration Date

Until further notice

Requirements

Must be able to obtain/maintain a DHS Suitability security clearance
Ph.D. or Masters’ degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences with at least one (1) year of laboratory bench experience outside of an academic environment, utilizing PCR, aseptic techniques, and biological assays
OR Bachelor’s degree from an accredited university requires four (4) years of laboratory bench experience outside of an academic environment
At least one (1) year of experience serving as a Senior Scientist or Team Leader of a laboratory team/project

Job Responsibility

Handling, receipt, and processing of operational, Quality Assurance (QA), and proficiency test (PT) samples potentially containing biological threat agents
Performing non-research biological science work utilizing microbiological and molecular techniques, including, but not limited to, DNA extraction and real-time polymerase chain reaction (real-time PCR) to identify and characterize pathogenic bacterial and viral agents
Preparing reagents and samples
Familiarity with Good Laboratory Practice (GLP)
Decontamination of work spaces, including Biological Safety Cabinets (BSCs), hoods/air boxes, equipment, and other items associated with processing and analysis activities
Maintaining chain-of-custody
Interpretation of results
Data entry utilizing computerized or computer-linked systems
Performing routine equipment calibration, cleaning, assembly, and maintenance
Collecting, processing, and analyzing internal laboratory swipes/swabs for Quality Assurance/Quality Control (QA/QC) and contamination monitoring

What we offer

Health, dental, and vision insurance
Paid time off and holidays
Retirement benefits (including 401(k) matching)
Educational reimbursement
Parental leave
Employee stock purchase plan
Tax-saving options
Disability and life insurance
Pet insurance

Fulltime

Senior/Principal Scientist, Cell Biology

are recruiting for a Senior/Principal Scientist, Cell Biology to join a clinical...

Location

United Kingdom , West London

Salary:

Not provided

CK Group

Expiration Date

Until further notice

Requirements

Educated ideally to PhD level with substantial industry (biotech or pharmaceutical industry) experience in oncology cell biology
Experience developing and running mammalian cell assays and flow cytometry analyses
Ability to develop and follow protocols and to work collaboratively as part of a team with the potential to mentor and/or line manage others

Job Responsibility

Develop and execute cell-based assays, including complex co-culture assays
Direct research and work closely with programme leaders and senior management to develop project plans, timelines, setting budgets etc.
Advises colleagues in experimental approaches, mentors team members and provides solutions
Analyse, critique and record experimental data using appropriate software and electronic lab notebooks
Work effectively in a small team with cross-functional team members
Ensure compliance with laboratory safety guidelines and quality standards

Fulltime

Clin Research Reg Spt Spec II

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

24.91 - 34.87 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 1 year of relevant experience required
Or equivalent combination of education and experience
Fully adheres to applicable safety and/or infection control standards required
Understands and follows data integrity standards and processes required
Ability to effectively manage a higher volume of protocols preferred
Ability to effectively manage moderately complex research protocols/procedures preferred
Possesses a high degree of self-motivation preferred
Recognized ability to function independently preferred
Proficient in managing multiple and competing priorities/demands preferred
Detailed-oriented in record keeping and research documentation preferred

Job Responsibility

Responsible for the coordination and oversight of regulatory requirements of clinical research protocols
Develops increased learned skills, flexibility in performing duties, and assumes responsibility for a portfolio of clinical research protocols under the direction of the Principal Investigator (PI) and senior leaders
Prepares all regulatory documentation, document filing, tracking, and maintenance
Maintains all logs, including OnCore, according to University of Rochester (UR) and department Standard Operating Procedures (SOPs)
Collects all regulatory documents required to submit to the DWG and PRMC and collates essential regulatory documents within Complion
Prepares/drafts ICF and insert institutional language, ensuring language is consistent with protocol
Enters and loads all required documents to OnCore and Complion
Coordinates and validates the delegation log with the applicable DWG clinical research staff
Prepares and tracks submission to Institutional Review Board (IRB) (CIRB, RSRB, Commercial IRB), FDA, ClinicalTrials.gov, etc
Maintains regulatory records and necessary correspondence records

Fulltime

Senior Bioinformatics Scientist

The Senior Bioinformatics Scientist, with input from senior scientists and leade...

Location

United States , San Diego

Salary:

128000.00 - 192000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in bioinformatics, computational biology, computer science, mathematics, or related field
or Master’s degree in same fields plus 4 years of experience in lieu of a Ph.D.
or Bachelor’s degree in same fields plus 6 years of experience in lieu of Ph.D.
5+ years of industry or academia experience in bioinformatics
3+ years of experience in medical device/IVD, biotech, life science or pharmaceutical industry
Extensive experience in Linux-based HPC or cloud computing environments and associated tools
Ability to write custom code in at least three programming or scripting languages
Technical expert in the area of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics
Knowledge of product/assay research, design, or development
Working knowledge of statistical and mathematical methods in biology/genetics, including experience with statistical software, such as JMP or R

Job Responsibility

Conduct analyses within several product or technology areas and identify problems and discrepancies
Independently develop, plan, and analyze results of bench level experiments within several product or technology areas
effectively present and clearly communicate findings at data meetings, group meetings and project team meetings
Analyze research/experimental data, interpret the results, and provide insights into the next steps and the direction of the project
Independently develop methods and procedures for new assignments/study/experiments
Provide technical guidance to junior scientists in project teams
Manage bench-generated data and bioinformatics outputs within high performance computing (HPC) or cloud computing environment
Determine, utilize, and apply methods or technologies effectively and provide ideas for new techniques, when appropriate
Maintain knowledge of technological industry developments that could assist in completion of an assignment or aid in the development of new processes or procedures
Provide technical input and participate in decisions affecting project planning and experimental design

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Director, Clinical Affairs

In this role, you will lead the development and execution of clinical strategies...

Location

United States , Skaneateles Falls

Salary:

208000.00 - 286000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Minimum: BA/BS in scientific discipline with minimum of 10+ years clinical operations experience (pharmaceutical, biotechnology or medical device industry
medical device preferred)
Expertise in ICH/GCP, ISO 14155, US Federal Food and Drug Administration and European Regulatory Authority requirements, as applicable to a study (or the requirements within countries in which a study is conducted)
Well-established knowledge in overall product development process from Phase 1 through Phase 4 for medical device trials, including software validation as required
Possesses expert knowledge of research objectives, protocol design, and data collection standards
Experience reviewing monitoring reports. High experience/proficiency with clinical operations systems including EDC, CTMS, and eTMF
Able to monitor performance of team in maintaining system updates to allow for senior management reports
Applies current applications/systems to compile information for presentation or distribution
Identifies new uses of current systems or use of new applications to enhance the management capabilities of projects
Expertise in clinical aspects of regulatory submission procedures, e.g. NDA, CTD, IDE

Job Responsibility

Lead the development and execution of clinical strategies and clinical research programs that enable Baxter’s product innovation and market adoption
Drive clinical planning, study execution, regulatory compliance, and cross‑functional collaboration while overseeing CROs, study sites, budgets, and timelines
Provide leadership to the clinical affairs team, ensuring high‑quality study operations, safety oversight, and successful delivery of clinical evidence supporting Baxter’s global portfolio
Clinical Strategy Development: Gather business priorities for both pre-market (approval) and post market (evidence) needs for clinical research
Engage collaboratively with Medical Affairs, Marketing, Reimbursement, and R&D resources as required as inputs for priority needs and to advise the execution strategy
Develop strategy and make recommendations for approaches to meet goals for technology feasibility, product validation, claims substantiation or content supporting market adoption
Conduct Clinical Research: Responsible for the identification and management of necessary resources to successfully initiate and complete clinical trials
Lead Clinical Study Execution team(s) to develop clinical strategies (and project plan) to efficiently manage the project(s) and maintain regulatory compliance
Clinical Plan - Partner with the Medical Monitor, Regulatory Affairs and Commercial to prepare a clinical plan for each project. This includes preparing timelines and budgets for the clinical program
Clinical Trial Protocols - Facilitate preparation of protocols including study design, case report forms, study procedures

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Director Project Leadership

The Director of 2008 Product manages and sustains the product in the U.S. market...

Location

United States of America , Concord

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Masters (M.S.) Degree in a related technological field required
Doctoral (Ph.D.) Degree in a related technological field strongly preferred
Minimum 10+ years' related experience
5+ years' experience as a Manager
or 5+ years' experience in a senior managerial role
Strong and experienced manager in both direct and indirect people management
Effective negotiation and conflict resolution skills
Strong interpersonal skills
Experience successfully collaborating with internal and external stakeholders
Able to delegate activities and manage resources, as well as to multitask, prioritize, and meet deadlines

Job Responsibility

Leads the global product development group (PDG) in the Product Engineering Center (PEC)
Responsible for developing and leading product development teams
Responsible for global product design oversight for the PEC including harmonizing and sustaining global product designs
Conducts research and development towards innovative products and identifying new technology platforms
Applies in-depth understanding to lead multicultural cross-functional activities and project activities in a variety of geographic locations
Meets departmental and organizational objectives, facilitates issue resolution and performs managerial related duties
Provide strategic leadership of short- and long-term goals
In collaboration with other senior management, develop, implement, and maintain a global product development strategy
Develops detailed engineering and scientific specifications for major engineering projects
Prepares and presents to executive management project updates, design concepts, and other information as needed

What we offer

medical insurance
dental insurance
vision insurance
a 401(k) with company match
paid time off
parental leave
potential for performance-based bonuses depending on company and individual performance

Fulltime

Senior Researcher / Laboratory Leader

jobRxiv

Location:
Czechia , Ostrava

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 09, 2025

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