Job Description

Associate Director, Pharmacovigilance Planning and Innovations

Waltham, Massachusetts

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kaileras mission to advance novel therapies for obesity and related conditions. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.

Reporting to the Senior Vice President, Patient Safety and Pharmacovigilance, this individual will play a critical role in ensuring the operational effectiveness, project planning, and cross?functional alignment of global patient safety and pharmacovigilance activities. Lead and support the integration of innovative technologies, drive process optimization, and other cross?functional initiatives from concept to adoption. Combine knowledge of pharmacovigilance practices with strong project management, stakeholder leadership, and business acumen.

Required location: Waltham, MA (hub?based, onsite 3?4 days per week)

Responsibilities

• Coordinate and lead departmental planning activities for the PSPV organization including, e.g., headcount modeling, organizational design, and pharmacovigilance projects
• Lead end?to?end project management for PV initiatives, including system implementations, process improvements, compliance programs, and organizational change efforts
• Develop and maintain project plans, metrics, and dashboards to support PSPV strategies
• Support resource forecasting, alliance management, and vendor oversight
• Facilitate cross functional meetings, track actions, and ensure on?time execution of project deliverables
• Communicate project updates to internal and external stakeholders through clear status reports, presentations, and dashboards
• Ensure project outcomes align with PV strategy and broader corporate objectives
• Build strong working relationships with cross functional leaders to support a proactive and collaborative safety culture
• Manage and coordinate cross functional alignment for operational effectiveness and PV system/process evolution
• Develop and maintain the pharmacovigilance innovation roadmap aligned with cross functional initiatives and compliance requirements
• Assist with the development and implementation of innovative technical or procedural solutions to improve PSPV operational capabilities
• Facilitate the maintenance of governance structures (e.g., Medical Safety Board)
• Support in GCP and GVP inspection readiness and support audits

Required Qualifications

• 10+ years of experience in biotech, pharma or CRO with a demonstrated focus on pharmacovigilance, drug safety, or related field
• 3+ years of project or program management experience in a regulated environment
• Demonstrated project management skills with strong analytical and problem?solving capabilities
• Exceptional communication, stakeholder engagement, and change management skills
• Strong interpersonal, organizational, and strategic planning skills
• Experience working with outsourced vendors or Contract Research Organizations (CROs)
• Experience leading or supporting process improvement
• Adaptable to changing priorities and across multiple clinical trials and deliverables
• Adept at communicating departmental vision, effectively aligning activities and performance to achieve functional area goals in alignment with corporate objectives
• Proficient computer skills, including Word, PowerPoint, Excel, Visio, Power BI or similar.
• Proven experience working independently with minimal supervision
• Knowledge of global safety and PV regulations, guidelines, and industry standards (FDA, EMA, ICH, GVP)

Preferred Qualifications

• Experience in other areas of drug development such as regulatory affairs, quality assurance or alliance management
• Hands?on experience with safety databases (e.g., Argus), PV quality systems, and regulatory inspections
• Familiarity with AI/ML and NLP in regulated settings

Education

• Bachelors degree or equivalent in Life Sciences, Public Health, Business or other related fields is required. MBA, PhD, PharmD, RN or Masters degree are preferred.

Salary Range

$160,000 - $200,000 USD

This range represents the companys good?faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year?end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grantsbecause your well?being and future matter to us.

EQUAL EMPLOYMENT OPPORTUNITY INFORMATION

Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy?related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.

E?Verify: Kailera Therapeutics, Inc. uses E?Verify to confirm the identity and employment eligibility of all new hires.

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