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Remote Gcp Laboratories Jobs (NOW HIRING)

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114K - $165K/yr

... GCP/ISO 14155 requirements. * Develop and maintain study project plans, timelines, and risk ... Oversee vendor selection, contracting, and performance management for CROs, laboratories, imaging ...

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114K - $165K/yr

... GCP/ISO 14155 requirements. * Develop and maintain study project plans, timelines, and risk ... Oversee vendor selection, contracting, and performance management for CROs, laboratories, imaging ...

PICTOR LABS INC

$89K - $123K/yr

... laboratories to advance their digital pathology capabilities while reducing chemical waste ... Remote US Company: Pictor Labs Employment Type: Full-time Responsibilities * Design, development ...

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How much do remote gcp laboratories jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for remote gcp laboratories in the United States is $27.67, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $33.17 per hour, depending on experience, location, and employer.
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Remote Gcp Laboratories jobs near you
Associate Director, Early Development Quality Lead, R&D QA

Associate Director, Early Development Quality Lead, R&D QA

Alnylam Pharmaceuticals

Cambridge, MA • On-site, Remote

$164K - $222K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

Associate Director, Early Development Quality Lead, R&D QA
Overview
The Early Development Quality Lead is responsible for the strategic quality oversight of internal and external (outsourced) activities in support of nonclinical studies (GLP and non-GLP), IND enabling work, as well as the utilization of Biomarkers within development programs (preclinical and clinical).
This role will partner with Alnylam colleagues within Early Development, Bioanalytical, Nonclinical Writing, Research, and Clinical Research to provide quality support and oversight and ensure the identification, mitigation, and escalation of emerging quality risks and concerns.
This position will be located within the US and can be hybrid, onsite, or remote.
Key Responsibilities
  • Sets the strategic quality oversight direction for internal and outsourced laboratory activities supporting nonclinical studies (GLP and non-GLP), including toxicology, bioanalytical and biomarker data that supports IND submissions.
  • Establish and maintain quality oversight of external laboratories including Test Facilities, Test Sites, and Clinical Laboratories by implementing governance framework and ongoing performance monitoring.
  • Collaborate with nonclinical and clinical teams (in partnership with GCP Program Leads) to integrate quality considerations into the selection, contracting, and management of external labs.
  • Ensure internally developed and outsourced biomarker development / analytical work complies with internal quality system requirements and external regulatory standards including GCP, GLP, ICH, and OECD.
  • Refine and continuously implement robust, risk-based vendor oversight and audit program globally for nonclinical work. Lead the risk assessment and audit strategy for external laboratories and ensure planned audits are executed in alignment with the GCP/GLP yearly audit program.
  • Support the management of nonclinical and clinical lab focused quality issues arising from outsourced activities, including quality events, significant quality issues, and CAPA oversight.
  • Serves as the Quality escalation point for CRO/vendor quality issues and leads quality governance activities to ensure appropriate identification, issue escalation and the mitigation of emerging compliance risks.
  • Provides quality strategic direction for the functional evaluation of CRO or key vendor processes or process improvement opportunities.
  • Drive the strategic identification and implementation of process improvement opportunities within Alnylam's QMS, in support of early development and research.
  • Partners with Legal/Procurement for appropriate oversight language in contractual agreements and ensure compliance

Qualifications
  • Educated preferably in life sciences (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification or work experience. Master's degree in a science, technology or industry related discipline, preferred.
  • Minimum of 8 years of relevant experience, inclusive of bioanalytical and toxicology subject matter, as it relates to GLPs, GCPs and GCLPs.
  • Direct experience in the field of assay development and validation and familiarity with modern biomarker-based assays (e.g., PCR, ELISA, FISH) is preferred.
  • Prior experience in risk-based thinking, quality assurance, auditing, managing quality issues/escalations, or other relevant QMS elements.
  • Prior expertise in global GLP, GCP, GCLP regulations and guidance across regulatory bodies such as FDA, PMDA, European Union, MHRA, etc.

#LI-AB1 #LI-Virtual
U.S. Pay Range
$164,500.00 - $222,500.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

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