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Bioanalytical Study Lead Jobs (NOW HIRING)

Orum Therapeutics

Bioanalytical Scientist

Lexington, MA · On-site

$39.50 - $49.75/hr

... from lead optimization to IND filing. * Oversee in vitro and in vivo ADME studies, including ... Provide high-level technical oversight for hybrid bioanalytical workflows, specifically bridging ...

Orum Therapeutics

Bioanalytical Scientist

Lexington, MA · On-site

$39.50 - $49.75/hr

... from lead optimization to IND filing. * Oversee in vitro and in vivo ADME studies, including ... Provide high-level technical oversight for hybrid bioanalytical workflows, specifically bridging ...

Orum Therapeutics

Bioanalytical Scientist

Lexington, MA · On-site

$150 - $180/day

... from lead optimization to IND filing. * Oversee in vitro and in vivo ADME studies, including ... Provide high-level technical oversight for hybrid bioanalytical workflows, specifically bridging ...

Integratedcooling

Bioanalytical Scientist

Lexington, MA · On-site

$39.50 - $49.75/hr

... from lead optimization to IND filing. * Oversee in vitro and in vivo ADME studies, including ... Provide high-level technical oversight for hybrid bioanalytical workflows, specifically bridging ...

IQVIA

Associate BioServices Study Lead

Ithaca, NY · Hybrid

$64K - $133K/yr

Serve as the primary point of contact for external customers while providing scientific oversight throughout the lifecycle of bioanalytical projects. Working under Study Lead Management and in ...

IQVIA

Associate BioServices Study Lead

Ithaca, NY · Hybrid

$64K - $133K/yr

Serve as the primary point of contact for external customers while providing scientific oversight throughout the lifecycle of bioanalytical projects. Working under Study Lead Management and in ...

IQVIA, Inc.

Associate BioServices Study Lead

Ithaca, NY · On-site

$64K - $133K/yr

Serve as the primary point of contact for external customers while providing scientific oversight throughout the lifecycle of bioanalytical projects. Working under Study Lead Management and in ...

IQVIA

Associate BioServices Study Lead

Indianapolis, IN · On-site +1

$64K - $133K/yr

We are seeking an Associate BioServices Study Lead - Hybrid to join IQVIA Laboratories at ... Provide scientific oversight throughout the lifecycle of bioanalytical projects while delivering ...

5AM Ventures

Bioanalytical Scientist

Emeryville, CA · On-site

$140K - $170K/yr

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

LabConnect

Bioanalytical Program Lead - Sweden

Bioanalytical Program Lead LabConnect improves lives by partnering with pharmaceutical and biotech ... study demands of traditional to increasingly complex trials. Additionally, we provide Functional ...

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How much do bioanalytical study lead jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for bioanalytical study lead in the United States is $25.39, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $27.88 per hour, depending on experience, location, and employer.

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For Bioanalytical Study Lead jobs, the most frequently searched job titles are:

Infographic showing various Bioanalytical Study Lead job openings in the United States as of July 2026, with employment types broken down into 88% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $52,817 per year, or $25.4 per hour.

Director, Translational Bioanalytical Sciences

Bridgewater, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

About The Role

Director, Translational Bioanalytical Sciences (Clinical Development, Translation Bioanalytical Science). Lead development, validation, and strategic application of bioanalytical and biomarker assays supporting small molecules, biologics, and emerging mixed-modality therapeutics from early development through clinical evaluation.

What You'll Do
  • Provide scientific leadership and strategic oversight for development/qualification/validation/implementation of bioanalytical, biomarker, pharmacodynamic, immunogenicity, and translational assays across modalities.
  • Partner with cross-functional teams to develop and execute integrated Translational Bioanalytical and Biomarker strategies.
  • Serve as TBAS representative on global project teams for strategy, decisions, and regulatory interactions.
  • Lead assay development and validation (including via CROs/partners) ensuring compliance with FDA/EMA/ICH/CLSI (e.g., ICH M10).
  • Plan and oversee regulated/non-regulated bioanalytical testing supporting preclinical and clinical studies.
  • Support clinical study design with input into protocols, SAPs, lab manuals, biomarker plans, and sample management.
  • Author/review scientific input to INDs, CTAs, NDAs, BLAs, PMAs, Investigator’s Brochures, Briefing Books, Clinical Study Reports, and other submissions.
  • Interpret and integrate data to inform dose selection, proof-of-mechanism/bio(ology), patient stratification, and key decisions.
  • Establish vendor governance; oversee external CROs/contract labs for quality, compliance, budget, and timelines.
  • Mentor and provide technical leadership; drive adoption of emerging technologies.
Who You Are (Qualifications)
  • PhD in Analytical Chemistry, PK, Pharmacology, Pharmaceutics, Bioanalytical Sciences, or related field.
  • 10+ years progressive biopharma/pharma experience in translational sciences, bioanalysis, biomarkers, and clinical development.
  • Leadership experience building/mentoring scientific teams.
  • Expertise in advanced bioanalytical technologies, especially LC-MS/MS, across modalities.
  • Experience in regulated and non-regulated bioanalytical study design/management/interpretation.
  • Strong knowledge of method development/qualification/validation/lifecycle management and regulatory guidance.
  • Experience managing CRO/partner governance and outsourcing.
  • Broad understanding of drug development and translating science to development/registration strategy.
  • Track record across global cross-functional project teams.
  • Deep regulatory knowledge (bioanalytical, biomarkers, immunogenicity) including health authority interactions and filings (IND/CTA/NDA/BLA/global submissions).
Benefits (U.S. offerings)
  • Medical, dental, vision, mental health support, wellbeing reimbursement, EAP.
  • Paid time off; fertility/family-forming, caregiver support; flexible schedules with purposeful in-person collaboration.
  • 401(k) with match; annual equity awards; ESPP; company-paid life/disability.
  • Learning/mentorship via Company Learning Institute; resource groups and recognition.
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