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Bioanalytical Outsourcing Jobs (NOW HIRING)

SPECTRAFORCE

Research Scientist

Redwood City, CA

... Outsourcing Services, which are powered by our Global Delivery Model with teams based onsite in the US Specific Responsibilities Design, development of bioanalytical assays and subsequent sample ...

Spectra force

Research Scientist

Redwood City, CA · On-site

... Projects Outsourcing Services, which are powered by our Global Delivery Model with teams based onsite in the US Specific Responsibilities • Design, development of bioanalytical assays and ...

5AM Ventures

QC Analytical Scientist

Emeryville, CA · On-site

$140K - $170K/yr

Design and manage outsourced bioanalytical studies * Critically review assay development, validation, and sample analysis * Identify deficiencies in methods, data quality, or interpretation and drive ...

5AM Ventures

QC Analytical Scientist

Emeryville, CA · On-site

$140K - $170K/yr

Design and manage outsourced bioanalytical studies * Critically review assay development, validation, and sample analysis * Identify deficiencies in methods, data quality, or interpretation and drive ...

Legend Biotech USA, Inc.

Ensure outsourced activities meet Legend quality standards, regulatory expectations, and program ... Contribute to bioanalytical sections of IND and other regulatory submissions.Cross-Functional ...

General Proximity

Head of DMPK

San Francisco, CA · On-site

Establish and manage CRO partnerships for outsourced ADME studies, including vendor qualification, scientific oversight, and data quality assurance. Bioanalytical Sciences * Own or oversee ...

General Proximity

Head of DMPK

San Francisco, CA · On-site

Establish and manage CRO partnerships for outsourced ADME studies, including vendor qualification, scientific oversight, and data quality assurance. Bioanalytical Sciences * Own or oversee ...

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Bioanalytical Outsourcing information

What are some common challenges faced when managing bioanalytical outsourcing projects, and how can they be addressed?

One common challenge in bioanalytical outsourcing is ensuring clear communication and alignment of expectations between the sponsor and the contract research organization (CRO). Differences in quality standards, timelines, and regulatory requirements can lead to delays or data discrepancies. To address these issues, it's important to establish detailed contracts, conduct regular progress meetings, and implement robust quality control processes. Building strong relationships with CRO partners and having contingency plans can greatly improve project outcomes and help mitigate risks.

What are the key skills and qualifications needed to thrive in Bioanalytical Outsourcing, and why are they important?

To thrive in Bioanalytical Outsourcing, you need a strong background in analytical chemistry, pharmacokinetics, and regulatory compliance, often supported by a degree in life sciences or related fields. Familiarity with laboratory information management systems (LIMS), mass spectrometry, and Good Laboratory Practice (GLP) certifications is typical. Effective project management, attention to detail, and excellent communication skills help ensure coordination with internal teams and external partners. These skills are essential to maintain data integrity, meet regulatory standards, and deliver reliable results in a highly collaborative and compliance-driven environment.

What is the difference between Bioanalytical Outsourcing vs Bioanalytical Scientist?

AspectBioanalytical OutsourcingBioanalytical Scientist
RoleContracting external labs or vendors to perform bioanalytical testingConducting bioanalytical research and testing within a company or lab
CredentialsTypically no specific credentials required; vendor qualifications varyRequires degrees (BSc, MSc, PhD) in relevant fields, with certifications often preferred
Work EnvironmentExternal labs, CROs, or contract vendorsIn-house laboratory or research facility
Industry UsageUsed by pharmaceutical companies outsourcing testing servicesEmployed within biotech or pharma companies conducting bioanalytical research

Bioanalytical Outsourcing involves contracting external labs for testing, while Bioanalytical Scientists perform testing within a company's lab. Both roles are essential in drug development, but they differ in responsibilities, work environment, and credentials.

What is bioanalytical outsourcing?

Bioanalytical outsourcing involves partnering with specialized external laboratories or service providers to conduct bioanalytical testing and analysis, usually as part of drug development and clinical trials. These services can include pharmacokinetic, pharmacodynamic, and biomarker analysis, among others. Outsourcing helps pharmaceutical and biotechnology companies access advanced technologies, expert staff, and regulatory-compliant processes without the need for in-house infrastructure. It can also speed up timelines and reduce costs associated with bioanalytical work.
What cities are hiring for Bioanalytical Outsourcing jobs? Cities with the most Bioanalytical Outsourcing job openings:
What states have the most Bioanalytical Outsourcing jobs? States with the most job openings for Bioanalytical Outsourcing jobs include:
What job categories do people searching Bioanalytical Outsourcing jobs look for? The top searched job categories for Bioanalytical Outsourcing jobs are:
Bioanalytical Outsourcing jobs near you
Infographic showing various Bioanalytical Outsourcing job openings in the United States as of June 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 87% In-person, 4% Hybrid, and 9% Remote job distribution.
Scientist, ADME & BioAnalytical

Scientist, ADME & BioAnalytical

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$135K - $175K/yr

Full-time

Posted 19 days ago

Job description

Overview
Monte Rosa Therapeutics (MRT) seeks to recruit an experienced, creative and highly talented DMPK and ADME Scientist who is eager will assit in leading the discovery and development effort to grow the drug pipelines, as well as help lead external GxP compliance research efforts. The Scientist will work MRTx colleagues to participate in all stages of DMPK and ADME assessments, from initial compound screening through to IND and NDA regulatory submissions. Working with Research, Bioanalytical and Clinical Science subject matter experts, provides scientific expertise to ensure that clinical candidates with acceptable drug development characteristics are identified and appropriately characterized. Represents Preclinical Development on Research and Development teams and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of DMPK and ADME findings
Responsibilities
  • Work closely with the medicinal chemistry team, the Scientist Position will lead the Nonclinical Development efforts in troubleshooting and guidance to the discovery project team with a particular focus on optimizing properties for oral administration
  • Represent Nonclinical Development to project teams and present our work in the interpretation of ADME experimental data related to the in vitro and in vivo animal PK and biotransformation.
  • Continually learn in vitro ADME and in vivo animal PK analysis (Winnolin)
  • Coordinate outsourced in vitro and in vivo DMPK studies
  • Explore new technologies and capabilities in discovery DMPK space
  • Strong written and oral communication to support internal communication of data, study reports and regulatory documentation.
  • Ability to work on multiple projects in a matrixed organizational structure
  • Aide the Nonclinical Development & Clinical Pharmacology team's activities across multiple project phases, including lead discovery, lead optimization, and regulatory filings.

Qualifications
  • 7+ years of drug discovery industry experience in Drug Metabolism, Pharmacokinetics, Pharmaceutical Chemistry, Toxicology, or a related scientific discipline.
  • Effective management of internal and external collaborations/service providers (CROs)
  • Build relationships with peers and partners outside of Nonclinical Development & Clinical Pharmacology to enable high team performance.
  • Demonstrates novel, innovative solutions to challenging problems using an extremely high degree of scientific discretion, intuition, and integrity.
  • Strong collaboration and innovative skills across subject areas representing DMPK as a project team representative within the core team is a key requirement.

Experience in the design, conduct, and interpretation of in vitro and in vivo ADME and animal PK studies

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