Research Associate, Sample Management Job at Enveda (Boulder)

Research Associate, Sample Management

Join Enveda as a Research Associate, Sample Management in Boulder, CO, and help ...

Location

United States , Boulder

Salary:

80000.00 - 90000.00 USD / Year

Enveda

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Bioengineering, or related field
Proficiency with LIMS/ELN platforms, such as Benchling
Hands-on experience with liquid-handling robots and automated storage systems
Strong organizational skills and attention to detail
service-oriented mindset

Job Responsibility

Receive, organize, and maintain Enveda’s sample collection
Collaborate to enhance high-throughput processes for natural product plant materials, extracts and compound libraries
Ensure data integrity in LIMS/ELN systems and manage inventory across diverse storage conditions
Operate and program automated liquid-handling robots
engage in manual pipetting as required

What we offer

90% Medical, Dental, Vision
401k Match
Flexible PTO
Adoption Assistance

Fulltime

Jr Research Associate Compound Management

We have an opening for a highly motivated Jr Research Associate to join our comp...

Location

Italy , Pomezia

Salary:

Not provided

IRBM

Expiration Date

Until further notice

Requirements

Diploma
Over two years of industrial experience is a plus
Good knowledge of the MS Office™ package (Excel ™
PowerPoint ™
Word ™
Outlook ™)
Good knowledge of common purification techniques and analytical techniques (UPLC/HPLC and mass spectrometry)
Good understanding of associated software is desirable (MassLynx, Empower)
Strong organizational and record keeping skills
Attention to details and accurate record keeping

Job Responsibility

Proactively contribute to the logistical aspects of compound management including: Sample inventory, reformatting, analysis, tracking and storage
Accurate record keeping
Dispatch samples internally or to external partners
Purification of final compounds and intermediates using mass directed HPLC
Close liaison with IRBM’s logistical team and Procurement

Senior Research Associate- Diagnostic Assay Development

10x Genomics is establishing a diagnostics effort, translating our leading singl...

Location

United States , Pleasanton

Salary:

97700.00 - 132100.00 USD / Year

10x Genomics

Expiration Date

Until further notice

Requirements

B.S. or M.S. in Molecular Biology, Genetics, Biochemistry, or a related scientific field
B.S. with 5+ years or M.S. with 3+ years of hands-on experience in molecular diagnostics or genomics assay development in an industry setting
Direct, demonstrable experience with advanced molecular technologies, particularly Next-Generation Sequencing (NGS) workflows
Exceptional proficiency in molecular biology techniques, including nucleic acid extraction, PCR/qPCR, and NGS library preparation
A proven track-record of using and optimizing and troubleshooting molecular biology protocols
Experience working with challenging clinical sample types (e.g., FFPE tissue, primary tumor cells, low-input samples)
Experience working within a quality system or environment governed by CLIA, CAP, or ISO 13485 standards strongly preferred
Prior hands-on experience with 10x Genomics single-cell or spatial technologies (e.g., Chromium or Xenium platforms) is a strong advantage
Experience with automated liquid handling for high-throughput assay execution is a strong advantage
experience with microscopy techniques a plus

Job Responsibility

Hands-on execution of complex single-cell and spatial genomics assays (e.g., sample processing, library preparation, sequencing)
Systematically troubleshoot, optimize, and refine specific steps within the assay workflow to improve performance, robustness, and efficiency
Perform feasibility studies on new reagents, instrumentation, and process improvements for clinical readiness
Prepare and process samples in support of large-scale clinical research studies
Generate and maintain meticulous laboratory records, protocols (SOPs), and batch records following Good Documentation Practices (GDP)
Execute formal experiments for analytical validation studies, including assessment of accuracy, precision, limit of detection, and reproducibility
Ensure all work is conducted under appropriate quality controls
Present experimental data clearly and concisely in team meetings and written reports
Support the transfer of robust assay workflows to the CLIA operations team
Collaborate closely with R&D Scientists, Automation Engineers, and Bioinformatics teams to meet project milestones

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Health Package
Easy-to-use Benefits
Family oriented
Generous Time Off

Fulltime

Sr Research Associate - Analytical Development

Theradaptive is revolutionizing the field of therapeutic delivery with a pipelin...

Location

United States , Frederick

Salary:

Not provided

Theradaptive

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Biochemistry, Pharmaceutical Analysis, Biotechnology, or Analytical Chemistry
Bachelor's degree with at least 5 years or Master's degree with at least 3 years of industry laboratory experience
Hands-on experience with Chromatography (SEC-HPLC, RP-HPLC) and/or electrophoresis (cIEF, CE-SDS) techniques
Strong multitasking abilities, effective time management skills, and excellent organizational capabilities
Ability to work collaboratively in a team environment, with meticulous attention to detail
Ability to work in a laboratory and office setting full time
Ability to lift up to 40 lbs
Ability to work in a laboratory with chemicals and biochemicals and perform Biosafety Level 2 work

Job Responsibility

Assist in the development and optimization of analytical methods using Chromatography (SEC-HPLC, RP-HPLC), moisture/water content determination (including Karl Fisher) and/or electrophoresis (cIEF, CE-SDS) techniques for the release and characterization of biologics and drug product/medical devices
Execute laboratory experiments, including sample testing and characterization of biologics using chromatography, UV spectroscopy, electrophoresis, and/or immunoassay and cell-based assays
Perform sample testing, analyze data, interpret results, and contribute to the preparation of reports in various formats, including Laboratory Notebooks (LN), formal reports, and presentations
Assist in the creation and review of Standard Operating Procedures (SOPs) for test method procedures and laboratory equipment operation and execute method qualification and validation studies
Ensure proper qualification, calibration, and maintenance of laboratory equipment in accordance with established schedules
Adhere to cGMP requirements as necessary and uphold compliance with standard operating procedures to maintain quality standards
Collaborate effectively within a team environment, demonstrate attention to detail, and communicate effectively verbally and in writing
Use standard laboratory, data analysis, and GMP quality systems, including Excel, GraphPad Prism, Laboratory Notebooks (LN), instrument software, and electronic quality systems, to support analytical development, testing, data review, investigations, trending, and compliant documentation
Adherence to laboratory and workplace safety protocols, proper use of personal protective equipment (PPE), hazard identification and reporting, and comply with the company's safety policies
Undertake any additional duties and responsibilities as needed to support the objectives of the laboratory

Fulltime

Research Associate

This position supports clinical and translational research activities for advanc...

Location

United States , Columbus

Salary:

47000.00 - 54144.00 USD / Year

Beacon Hill

Expiration Date

Until further notice

Requirements

Bachelor's degree in a life science discipline (e.g., biology, biochemistry, or similar)
At least 2 years of experience supporting clinical research activities, sample operations, or research operations within a regulated environment
Familiarity working under FDA, ICH, and GCP/GLP guidelines
Demonstrated ability to manage confidential and sensitive information responsibly
Strong organizational and prioritization skills with comfort working in a changing, deadline-driven setting
Proven attention to detail in handling clinical or research samples in accordance with controlled procedures
Collaborative working style with the ability to engage effectively across multiple functional teams
Clear verbal and written communicator, capable of translating technical concepts for varied audiences
Experience contributing to process documentation, training materials, or procedural improvements
Motivation to work within a fast-moving research environment focused on advancing patient-impacting therapies

Job Responsibility

Support clinical and translational research initiatives related to novel modality programs, including gene-based and RNA-focused therapies
Coordinate the movement, tracking, and reconciliation of biological samples associated with clinical studies
Maintain accurate documentation and records within both electronic systems and controlled paper files
Contribute to the design, rollout, and ongoing maintenance of centralized systems used for sample inventory, consent status, and tracking
Oversee day-to-day sample lifecycle activities, ensuring traceability and data accuracy
Assist with logistics and accountability for clinical study materials and supplies
Perform work in alignment with applicable regulatory standards, including GCP and GLP requirements
Develop, update, and organize materials and training resources used by clinical collection sites
Work closely with internal teams and external partners to support data exchange, downstream analysis, and operational reporting
Serve as a point of contact for coordination with vendors, service providers, and research collaborators

Fulltime

Research Associate I/II, Production

BigHat Biosciences is seeking a self-motivated individual for a Research Associa...

Location

United States , San Mateo

Salary:

75000.00 - 105000.00 USD / Year

BigHat Biosciences

Expiration Date

Until further notice

Requirements

BS in Biology or Chemistry, with 1+ year(s) of industry experience
Experience in process execution, laboratory method development, optimization, and troubleshooting
Hands-on experience with, or interest in, automated liquid handlers (e.g. Hamilton, OpenTrons, Tecan, Agilent systems)
Experience with molecular biology techniques and general lab practices
Efficient time management and ability to work on several projects simultaneously, in a dynamic start-up environment
Strong interpersonal skills and ability to effectively communicate with members of a multidisciplinary team
Excellent record keeping abilities to document experimental work and analytical data

Job Responsibility

Perform automated and manual high-throughput processing on the BigHat platform, including DNA preparation, protein expression, and protein characterization
Contribute to the scaling up of BigHat's platform and production-grade data generation
Support BigHat's Platform Reagents & Assay Support (PRAS) function by contributing to in-house reagent manufacturing efforts
Execute experiments to optimize the performance efficiency of BigHat's platform
Keep a detailed record of all experiments using BigHat's documentation tools, and clearly communicate results and challenges
Collaborate on the creation of laboratory standard operating procedures (SOPs) for sample processing
Collaborate closely with BigHat team members to identify, design, and implement critical process and operational improvements to production workflows and laboratory systems
Operate automated liquid handlers and analytical instruments to ensure all lab and platform operations run efficiently

What we offer

Range of health insurance plan options through Anthem and Kaiser (monthly credit if benefit waived)
Dental, and vision coverage through Guardian
Additional well-being benefits through Nayya, OneMedical, Wagmo, Rula, and more
401(k) with company match
DTO, two weeks of company-wide shutdown, and 12 company holidays
Paid parental leave
bonus
options

Fulltime

Research Associate, In Vivo

Help bring science to life and join a leading pharmaceutical company to play a k...

Location

United States , Cambridge

Salary:

36.00 - 40.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

Background in biology or a related field, with hands-on experience in laboratory rodent research
Proficiency in dose administration techniques for rats and mice (e.g., SC, IV, PO, IT, IM)
Skilled in blood collection methods (e.g., tail vein, submandibular, terminal collection)
Ability to identify and document abnormal behavior and clinical signs in rodents
Strong mathematical skills for calculating dilutions and dose projections
Proficiency in MS Word, Excel, PowerPoint, and GraphPad Prism
experience with electronic data capture systems is a plus
Knowledge of rat and mouse anatomy for necropsies and tissue collections
Familiarity with applicable Animal Welfare Guidelines
Certification as an Assistant Laboratory Animal Technician (ALAT) or Laboratory Animal Technician (LAT) is advantageous

Job Responsibility

Coordinate pre-study activities, including protocol development, test article procurement, and animal ordering
Perform dose calculations and prepare dosing solutions
Conduct study procedures such as dosing, monitoring clinical signs, recording body weights, collecting blood samples, performing necropsies, and tissue collections on mice and rats
Utilize Excel spreadsheets or electronic data capture systems to collect and manage study data
Perform quality control checks on study data
Draft initial study reports and collaborate with Principal Investigators to finalize them
Create graphs of key study parameters using Excel or GraphPad Prism
Communicate effectively in group meetings and research discussions, while managing conflicts professionally
Maintain a safe and clean working environment by adhering to procedures, rules, and regulations
Adapt quickly to changing priorities in a dynamic work environment

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale, California

Salary:

20.00 - 27.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Customer service experience in a fast-paced environment
Clinical Research experience or patient experience is required
B.S.+ in related life science field OR HS diploma or GED with experience
Comfortable standing and walking for a prolonged period of time
Required: fluent in spoken and written English as well as Mandarin

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Extensive induction program and ongoing training
Career advancement support
Market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings
Annual performance-based bonus plan (for eligible roles)
Annual salary review
Additional total rewards incentives (for eligible roles)

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Research Associate, Sample Management

Requirements

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