Clinical Research Analyst IV

Master’s degree in an appropriate area and two years of relevant experience; or a Bachelor’s degree in an appropriate area and four years of relevant experience; or an equivalent combination of education and experience.

The Regulatory Lead for Internal CRO Trial Design & Implementation provides regulatory and operational leadership for Clinical Research Hub (CRH)-supported clinical trials from concept development through study activation and implementation. The Lead functions as a regulatory subject matter expert within CRH's internal CRO model, partnering with investigators and cross-functional research teams to translate scientific concepts into feasible, compliant protocols and execution plans. This crucial role coordinates with investigators, biostatistics, data management, pharmacy, finance, contracts, compliance, and other institutional partners to support efficient, compliant study execution.

Essential Functions:

Trial Design and Regulatory Strategy:

• Lead regulatory and operational consultation during concept and protocol development for investigator-initiated and other CRH-supported clinical trials.
• Review study design, objectives, endpoints, eligibility criteria, intervention plans, safety monitoring, schedules of assessments, data collection, and operational feasibility.
• Assess regulatory pathways and submission requirements, including IRB strategy, sponsor-investigator responsibilities, and IND/IDE considerations when applicable.
• Identify design or compliance gaps early and develop practical mitigation plans with investigators and CRH partners.

Study Start-Up and Implementation:

• Translate approved protocols into coordinated implementation plans and lead regulatory readiness through activation.
• Coordinate required approvals, essential documents, study-specific plans, delegation and training requirements, and cross-functional start-up activities with data management, pharmacy, laboratory, finance, contracts, and clinical operations.
• Confirm that regulatory and operational requirements are complete before study launch and support structured handoff into active study conduct.

Internal CRO Regulatory Operations and Project Management:

• Serve as the regulatory lead for an assigned portfolio of internal CRO projects.
• Maintain submission and activation timelines, regulatory trackers, essential documentation, and status reporting.
• Coordinate initial submissions, amendments, continuing review, reportable events, and other regulatory deliverables as applicable.
• Manage dependencies, escalate barriers, and facilitate decisions across investigators and institutional stakeholders to keep studies moving toward planned milestones.

Quality, Compliance, Training, and Inspection Readiness:

• Perform quality review of protocols, submissions, regulatory files, and implementation materials for consistency with applicable regulations, ICH GCP, IRB requirements, and institutional policy.
• Develop and maintain SOPs, templates, checklists, and training resources for the internal CRO.
• Provide regulatory education and consultation to investigators and research teams, support corrective action and process improvement, and promote ongoing inspection readiness.

Staff Supervision and Program Improvement:

• Provide direct supervision to the assigned Clinical Research Analysts (CRAs), including work assignment, prioritization, coaching, quality review, performance feedback, and professional development support.
• Standardize internal CRO regulatory and trial implementation workflows, monitor service performance, and lead process improvements that increase consistency, efficiency, and accountability across the program.

$90,000 - $95,000 annually; commensurate with education and experience.

Master’s degree in an appropriate area and two years of relevant experience; or a Bachelor’s degree in an appropriate area and four years of relevant experience; or an equivalent combination of education and experience.

• Bachelor's degree in clinical research, regulatory affairs, health sciences, public health, or a related field; advanced degree preferred.
• Four or more years of progressively responsible experience in clinical research regulatory operations, study start-up, or clinical trial management.
• Demonstrated experience with protocol development, trial design review, and operational feasibility assessment.
• Experience supporting FDA-regulated and/or investigator-initiated clinical trials, including IND/IDE and sponsor-investigator responsibilities when applicable.
• Strong working knowledge of ICH GCP, IRB requirements, applicable FDA regulations, and institutional human research protection processes.
• Experience coordinating study activation and cross-functional implementation across regulatory, data management, pharmacy, laboratory, finance, contracts, and clinical operations.
• Experience in a CRO, academic research organization, sponsor operations group, or comparable multi-study clinical research environment.
• Experience developing SOPs, regulatory templates, quality review processes, and study start-up tools.
• Strong project management skills with demonstrated ability to manage multiple studies, deadlines, dependencies, and stakeholders.
• CCRP, CCRC, RAC, PMP, or equivalent clinical research, regulatory, or project management certification preferred.
• Experience serving as a team lead, supervisor, or work lead and providing training, coaching, work assignment, and deliverable review for research staff or analysts.

In order to be considered, you must upload your cover letter and resume.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.