GCP Consultant (AD-level) Job at Redbock - an NES Fircroft company in Lexington
Redbock - an NES Fircroft company, Lexington, MA, United States
Our client is a
global biopharmaceutical company
focused on discovering, developing, and commercializing
immune‑modulating therapies
for patients with debilitating diseases and significant unmet medical need.
Status:
Hybrid-1 day WFH will be Friday
The contractor will provide advanced GCP compliance and clinical quality support, ensuring clinical trials are executed in alignment with global regulatory requirements, internal SOPs, and industry best practices. This role requires a seasoned professional capable of driving compliance initiatives, collaborating cross‑functionally, and serving as a key quality partner to Clinical Operations and external vendors.
Key Responsibilities Clinical Quality & GCP Compliance
Provide
expert-level GCP oversight
to ensure clinical trials are planned, executed, and documented in full compliance with ICH‑GCP, study protocols, and internal quality standards.
Conduct
comprehensive reviews of trial documentation
(eTMF, protocols, monitoring reports, site documents) to identify GCP gaps and ensure inspection readiness.
Lead and support the management of
compliance issues , including identification, escalation, and coordination of corrective/preventive actions (CAPAs).
Audit Leadership
Serve as a key contributor to the
audit program , including trial audits and system audits.
Conduct and/or support
vendor audits , ensuring CROs, laboratories, and other third parties operate in full compliance with contractual and regulatory requirements.
Assist in preparing teams, documents, and systems for
regulatory inspections .
Cross‑Functional Collaboration
Work closely with
Quality Assurance ,
Clinical Operations , and cross‑functional study teams to ensure alignment, quality consistency, and proactive resolution of compliance issues.
Partner with external vendors to monitor compliance performance and drive continuous improvement.
Experience Requirements
Several years of hands‑on experience in
GCP, clinical quality, auditing, or clinical compliance roles , preferably within biotech or pharmaceutical environments.
Strong knowledge of
ICH‑GCP, FDA, EMA, and global regulatory expectations .
Demonstrated ability to act as a
“heavy hitter” —independent, knowledgeable, and capable of making decisions and driving quality outcomes in a complex clinical environment.
Our ideal candidate is a self‑motivated individual who has a passion for clinical quality and can thrive in a fast‑paced dynamic environment. The Associate Director GCP Quality is responsible for leading Clinical Quality Assurance (CQA) activities for clinical development programs, including the management of audits, quality issues and investigations, and inspections. This position requires a depth of understanding and significant experience in GCP and compliance, leadership, and communication skills to conduct responsibilities independently. This role is accountable for Good Clinical Practice (GCP), Good Laboratory Practice (GLP) and/or Pharmacovigilance (PV) oversight, and for assuring the compliance of studies with our Company's Standard Operating Procedures (SOPs), policies, and all applicable worldwide regulations and guidelines (e.g., United States FDA, European Union Directives, ICH, and National regulations).
This role is based in our Lexington, MA office. Our office‑based employees follow a hybrid schedule of 4 days in the office, and 1 day remote. Remote arrangements may be considered for highly qualified individuals.
Responsibilities ( Including, But Not Limited To )
Provide professional expertise and guidance on GCP, GLP and Good Pharmacovigilance Practices (GPV) regulations and other applicable regulations to clinical development teams to proactively identify compliance issues/risks and recommend mitigations
Provides clinical quality strategy
Fosters a collaborative working relationship with key stakeholders (e.g., regional study team members, global clinical operations compliance team members, etc.)
Liaise with various functions and external parties including contract auditors and investigator sites to promote a high level of quality and consistency across and within programs; develop the risk‑based audit and compliance strategy for programs; assist project teams in implementing corrective and preventive actions; and enable teams to be inspection ready, in support of a culture of sustainable compliance
Support GCP audit program to include routine and non‑routine quality assurance audits of clinical investigator sites, vendors, processes, systems, and study documents to ensure integrity and accuracy of study data and assure quality compliance with internal procedures as well as regulatory guidelines.
Support Oversight of the Commercial Pharmacovigilance Program
Develop and implement program‑specific risk‑based audit and compliance strategy and manage audits of sites, documents, databases, vendors or internal systems in compliance with GCP/GLP/GPV and the client’s policies and procedures.
Lead investigations into significant quality issues, scientific misconduct and serious breach of GCP/GLP/GPV, if they occur; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities
Lead and support GCP/GLP/GPV health authority inspections; lead clinical development teams in preparation for announced inspections and provide GCP compliance technical support during inspections of investigator sites and the client
Provide Clinical QA oversight of GCP protocols, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), and other clinical trial specific documents as requested.
Analyze, report, and present metrics for assigned programs to development teams, R&D, and Quality management; recommend any required actions and monitor implementation
Collaborate with Quality team to identify and mitigate GCP/GLP/GPV quality and compliance issues with potential impact across multiple programs or functional groups
Escalate systemic and/or critical problems and recommend appropriate solutions to senior management for immediate and long‑term resolution
Stays abreast of new and revised government, industry and company regulations, trends and interpretations by participating in trainings, conferences, workshops and discussion groups as appropriate
Other duties as assigned
Qualifications And Experience
B.S degree in life sciences with 10+ years of progressive global quality/regulatory compliance background in pharma/biotech or medical device industries, with a hands‑on role in clinical quality operations and quality system preferred
Advanced degree (MS, PhD, MBA) preferred. In lieu of advanced degree, additional years of equivalent experience will be considered.
Auditor certifications a plus.
Requires solid experience supporting Phases I-IV (particularly Phase III); experience with Regulatory submissions and/or approval.
Experience with effectively managing regulatory agency inspection and working with regulators and internal staff to help prepare for inspections is required.
Experience developing SOPs, reviewing internal clinical, regulatory and medical processes to ensure they are accurately represented in current SOPs is essential.
Broad knowledge of risk‑based quality systems approaches consistent with ICH E6 and ICH E8
Previous hands‑on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS required
A strong customer focus and ability to prioritize and adapt to business needs are required
Strong business partner with a focus on collaborating and delivering results
Self‑motivated, detail oriented, well organized, and able to demonstrate success with managing multiple projects simultaneously and other priorities
Understanding and knowledge of applicable industry regulations
Ability to interact constructively and efficiently within and across functional areas and management
Ability to resolve day‑to‑day issues efficiently while maintaining compliance
Provide imaginative, thorough, and practical solutions to problems
Solve conflict and address workplace issues in professional and collaborative manner
#J-18808-Ljbffr
global biopharmaceutical company
focused on discovering, developing, and commercializing
immune‑modulating therapies
for patients with debilitating diseases and significant unmet medical need.
Status:
Hybrid-1 day WFH will be Friday
The contractor will provide advanced GCP compliance and clinical quality support, ensuring clinical trials are executed in alignment with global regulatory requirements, internal SOPs, and industry best practices. This role requires a seasoned professional capable of driving compliance initiatives, collaborating cross‑functionally, and serving as a key quality partner to Clinical Operations and external vendors.
Key Responsibilities Clinical Quality & GCP Compliance
Provide
expert-level GCP oversight
to ensure clinical trials are planned, executed, and documented in full compliance with ICH‑GCP, study protocols, and internal quality standards.
Conduct
comprehensive reviews of trial documentation
(eTMF, protocols, monitoring reports, site documents) to identify GCP gaps and ensure inspection readiness.
Lead and support the management of
compliance issues , including identification, escalation, and coordination of corrective/preventive actions (CAPAs).
Audit Leadership
Serve as a key contributor to the
audit program , including trial audits and system audits.
Conduct and/or support
vendor audits , ensuring CROs, laboratories, and other third parties operate in full compliance with contractual and regulatory requirements.
Assist in preparing teams, documents, and systems for
regulatory inspections .
Cross‑Functional Collaboration
Work closely with
Quality Assurance ,
Clinical Operations , and cross‑functional study teams to ensure alignment, quality consistency, and proactive resolution of compliance issues.
Partner with external vendors to monitor compliance performance and drive continuous improvement.
Experience Requirements
Several years of hands‑on experience in
GCP, clinical quality, auditing, or clinical compliance roles , preferably within biotech or pharmaceutical environments.
Strong knowledge of
ICH‑GCP, FDA, EMA, and global regulatory expectations .
Demonstrated ability to act as a
“heavy hitter” —independent, knowledgeable, and capable of making decisions and driving quality outcomes in a complex clinical environment.
Our ideal candidate is a self‑motivated individual who has a passion for clinical quality and can thrive in a fast‑paced dynamic environment. The Associate Director GCP Quality is responsible for leading Clinical Quality Assurance (CQA) activities for clinical development programs, including the management of audits, quality issues and investigations, and inspections. This position requires a depth of understanding and significant experience in GCP and compliance, leadership, and communication skills to conduct responsibilities independently. This role is accountable for Good Clinical Practice (GCP), Good Laboratory Practice (GLP) and/or Pharmacovigilance (PV) oversight, and for assuring the compliance of studies with our Company's Standard Operating Procedures (SOPs), policies, and all applicable worldwide regulations and guidelines (e.g., United States FDA, European Union Directives, ICH, and National regulations).
This role is based in our Lexington, MA office. Our office‑based employees follow a hybrid schedule of 4 days in the office, and 1 day remote. Remote arrangements may be considered for highly qualified individuals.
Responsibilities ( Including, But Not Limited To )
Provide professional expertise and guidance on GCP, GLP and Good Pharmacovigilance Practices (GPV) regulations and other applicable regulations to clinical development teams to proactively identify compliance issues/risks and recommend mitigations
Provides clinical quality strategy
Fosters a collaborative working relationship with key stakeholders (e.g., regional study team members, global clinical operations compliance team members, etc.)
Liaise with various functions and external parties including contract auditors and investigator sites to promote a high level of quality and consistency across and within programs; develop the risk‑based audit and compliance strategy for programs; assist project teams in implementing corrective and preventive actions; and enable teams to be inspection ready, in support of a culture of sustainable compliance
Support GCP audit program to include routine and non‑routine quality assurance audits of clinical investigator sites, vendors, processes, systems, and study documents to ensure integrity and accuracy of study data and assure quality compliance with internal procedures as well as regulatory guidelines.
Support Oversight of the Commercial Pharmacovigilance Program
Develop and implement program‑specific risk‑based audit and compliance strategy and manage audits of sites, documents, databases, vendors or internal systems in compliance with GCP/GLP/GPV and the client’s policies and procedures.
Lead investigations into significant quality issues, scientific misconduct and serious breach of GCP/GLP/GPV, if they occur; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities
Lead and support GCP/GLP/GPV health authority inspections; lead clinical development teams in preparation for announced inspections and provide GCP compliance technical support during inspections of investigator sites and the client
Provide Clinical QA oversight of GCP protocols, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), and other clinical trial specific documents as requested.
Analyze, report, and present metrics for assigned programs to development teams, R&D, and Quality management; recommend any required actions and monitor implementation
Collaborate with Quality team to identify and mitigate GCP/GLP/GPV quality and compliance issues with potential impact across multiple programs or functional groups
Escalate systemic and/or critical problems and recommend appropriate solutions to senior management for immediate and long‑term resolution
Stays abreast of new and revised government, industry and company regulations, trends and interpretations by participating in trainings, conferences, workshops and discussion groups as appropriate
Other duties as assigned
Qualifications And Experience
B.S degree in life sciences with 10+ years of progressive global quality/regulatory compliance background in pharma/biotech or medical device industries, with a hands‑on role in clinical quality operations and quality system preferred
Advanced degree (MS, PhD, MBA) preferred. In lieu of advanced degree, additional years of equivalent experience will be considered.
Auditor certifications a plus.
Requires solid experience supporting Phases I-IV (particularly Phase III); experience with Regulatory submissions and/or approval.
Experience with effectively managing regulatory agency inspection and working with regulators and internal staff to help prepare for inspections is required.
Experience developing SOPs, reviewing internal clinical, regulatory and medical processes to ensure they are accurately represented in current SOPs is essential.
Broad knowledge of risk‑based quality systems approaches consistent with ICH E6 and ICH E8
Previous hands‑on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS required
A strong customer focus and ability to prioritize and adapt to business needs are required
Strong business partner with a focus on collaborating and delivering results
Self‑motivated, detail oriented, well organized, and able to demonstrate success with managing multiple projects simultaneously and other priorities
Understanding and knowledge of applicable industry regulations
Ability to interact constructively and efficiently within and across functional areas and management
Ability to resolve day‑to‑day issues efficiently while maintaining compliance
Provide imaginative, thorough, and practical solutions to problems
Solve conflict and address workplace issues in professional and collaborative manner
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