Director, Clinical Operations

Director, Clinical OperationsThis position is responsible for the strategic planning, financial oversight, and end-to-end execution of clinical trials, while ensuring compliance with regulatory, quality, and internal standards. This role oversees CROs and other external vendors, manages cross-functional study teams, supports data integrity, and drives operational efficiencies to ensure studies are delivered on time, within approved budgets, and with high quality.Key responsibilities include:Clinical Trial Strategy & ManagementFormulate operational execution strategies for clinical programs spanning Phase I–IV trials.Is accountable for the operational delivery of clinical trials, from protocol development through completion of the clinical study report.Own the development, maintenance, and adherence to integrated study timelines and milestones.Proactively identify and interpret clinical trial risks and implement mitigation strategies/corrective actions to address them.Drive study-level site selection and patient recruitment strategies.Determine drug supply assumptions for clinical trials and ensure trial sites have adequate drug supply.CRO & Vendor OversightLead the identification, selection, and oversight of CROs, other external clinical vendors, and trial sites to ensure clinical trials are delivered on time, within approved budgets, and to expected quality standards.Serve as the primary oversight contact for strategic CRO and vendor partnerships.Lead contract and budget negotiations for CROs and other clinical vendors.Track metrics and performance to hold CROs and other clinical vendors accountable to financial and operational expectations.Manage clinical trial budgets and forecast costs across programs.Compliance & Quality AssuranceDevelop or assist in developing/reviewing clinical protocols, investigator brochures, clinical development plans, clinical portions of regulatory submissions, and other key study-related documents.Ensure study plans, case report forms, tables, listings, figures, and clinical study reports are consistent, complete, accurate, and aligned with study objectives and regulatory requirements.Ensure compliance with clinical protocols, study plans, GCP, ICH, FDA, and other applicable regulatory requirements during clinical trials.Maintain an ongoing state of inspection-readiness across trial master files and study documentation.Lead the development, review, and continuous improvement of clinical SOPs and operational processes to support compliant, efficient, and inspection-ready clinical trial execution.Team Leadership & Cross-Functional AlignmentPromote alignment across functions by collaborating with internal stakeholders and serving as a core member of the cross-functional study team.Provide direction, guidance, feedback, and mentoring to external partners, consultants, contractors, and study team members, as appropriate.Effectively influence and ensure seamless, two-way communication and information sharing with internal and external stakeholders (e.g., CROs and trial sites) to ensure well-coordinated team dynamics and study execution.Required Leadership Behaviors:We group these behaviors into three pillars:HEADThink EntrepreneuriallyTake Decisive ActionDrive ResultsHEARTCommunicate EffectivelyEnable High PerformanceCollaborate with PurposeGUTSTake Smart RisksBe Tenacious About ChangeCompete to WinSuccessful candidates will demonstrate these behaviors through their ability to challenge the status quo, build strong relationships, drive results, embrace change, and contribute to a high-performance culture.Qualifications:B.A. or B.S. with at least 8 years of clinical trial experience in a pharmaceutical or biotechnology company, including experience leading or overseeing clinical trial executionExpertise in clinical operations, with in-depth understanding of FDA regulations and ICH-GCP guidelines governing the conduct of clinical trialsExpertise in budgeting, financial tracking, and contract negotiationStrong organizational, problem-solving, and operational management skillsAbility to communicate effectively, both verbally and in writing, across various levels of the organizationProven ability to work collaboratively and effectively in a cross-functional environmentFlexibility to adapt to changing program and organizational needsProficiency with Microsoft Office (Excel, Outlook, PowerPoint, Word) and EDC systems requiredPay Range $215,000 - $253,000 USDCollegium is an equal opportunity employer. It is the policy of Collegium, in all of its relations with its employees and applicants for employment, to base all employment-related decisions upon valid job-related factors, without regard to age, national origin, citizenship status, ancestry, race, color, religion, creed, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or expression (including transgender status), sexual orientation, military or veteran status, physical or mental disability, genetic information, or any other status protected by applicable federal, state, or local law. This policy applies to hiring, training, promotion, compensation, disciplinary measures, access to facilities and programs, and all other personnel actions and conditions of employment. By this policy, Collegium seeks to ensure that all employees have the opportunity to make their maximum contribution to Collegium and to their own career goals. This policy provides for an equal employment opportunity program that will simultaneously serve the requirements of society, the law, sound business practices and individual dignity.If you have questions or concerns about equal employment opportunities in the workplace, you are encouraged to bring these issues to the attention of the Head of Human Resources. We will not allow any form of retaliation against employees who raise issues of equal employment opportunity. To ensure our workplace is free of artificial barriers, violation of this policy may result in disciplinary action, up to and including termination.