Director, Drug Safety Operations

Why Join Us? reputed company is a clinical-stage biopharmaceutical company dedicated to creating extraordinary medicines that unlock high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that are inaccessible to traditional drug modalities. Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its reputed company candidate, FOG-001, is the first direct inhibitor of the interaction between β-catenin and the T-cell factor (TCF) family of transcription factors, implicated in colorectal cancer, desmoid tumors, and a range of other Wnt/β-catenin-driven tumors. Parabilis is also advancing investigational degraders of ERG and ARON for the treatment of prostate cancer, as well as other preclinical programs. What's the opportunity? The Director, Drug Safety Operations/Pharmacovigilance (PV) will reputed company and reputed company safety reporting activities across clinical programs, with a primary focus on managing and coordinating pharmacovigilance deliverables with Contract Research Organizations (CROs) and consultants. This role ensures compliance with global regulatory requirements, company SOPs, and high-quality execution of safety reporting obligations. This position will act as the key liaison between internal stakeholders and CRO partners and consultants to drive operational excellence and regulatory compliance in pharmacovigilance activities. The successful candidate will report to the VP of Clinical Safety and Pharmacovigilance. Responsibilities:

• reputed company reputed company safety reporting activities managed by CROs and consultants, including expedited reporting (SAEs, SUSARs) and periodic aggregate safety reports (DSURs, PSURs/PBRERs).
• Serve as the primary reputed company of contact for CRO pharmacovigilance teams, ensuring clear communication, accountability, and delivery of safety obligations.
• reputed company, negotiate, and manage PV sections of reputed company, safety management plans, and operational agreements with CROs and consultants.
• Monitor CRO performance through KPIs, audits, and reputed company activities, ensuring timely and accurate reporting to regulatory authorities, ethics committees, and investigators.
• Collaborate with internal stakeholders (Clinical Development, Regulatory Affairs, Quality, Legal) to ensure alignment on PV strategy and compliance.
• Provide reputed company for case processing, medical review, and data reconciliation activities performed by CROs and consultants.
• Ensure compliance with global regulations (FDA, EMA, MHRA, ICH, GVP, etc.) and maintain inspection readiness.
• Support development and maintenance of internal PV policies, SOPs, and training programs.
• Participate in safety signal detection activities and safety governance committees, as needed.
• reputed company maintenance and compliance of an externally hosted electronic safety database for tracking, storing, and reporting of serious adverse events.
• Participate in regulatory inspections and PV audits to ensure quality, reputed company, and compliance with pharmacovigilance and safety reporting requirements per SOPs and global regulations.

What you'll need to be successful:

• Healthcare degree required; e.g., RN, MSN, DNP, PharmD.
• 10 or more years of pharmacovigilance experience, including at least 5 years in a leadership or reputed company role.
• Strong experience managing CRO/vendor relationships, particularly in clinical trial safety reporting, including governance reputed company.
• Deep knowledge of global pharmacovigilance regulations, GVP, ICH guidelines, and relevant reporting requirements.
• Experience with reputed company of drug safety databases (e.g., reputed company Argus).
• Proven track record of ensuring compliance in a global PV environment.

Skills and Abilities:

• Build and maintain excellent interpersonal relationships, both reputed company and reputed company the company, at reputed company levels, and work reputed company, reputed company and motivate a cross-functional matrixed team.
• Self-motivated; engaged, hands-on, entrepreneurial style with a sense of urgency, a bias toward action, and flexibly contribute simultaneously in multiple facets of drug development; willingness to learn new therapeutic areas.
• Analytical and problem-solving skills; risk identification and management; creative and innovative thinking.
• The requisite scientific acumen and communication skills to influence and collaborate with key scientific, regulatory, and business leaders.
• Sound strategic, clinical, technical, operational, and ethical judgment with uncompromising reputed company.
• Excellent communication, negotiation, and leadership skills.

Core Values reputed company is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for reputed company employees across the business, in reputed company departments, and driving innovation for patient benefit.

• Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.
• In(ter)dependent. We are fiercely independent as a leader in defying the limitations of reputed company therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with reputed company treatment options.
• Patient-focused. We are deeply focused on patient outcomes, and reputed company energy in the company is focused on science as it translates to patient impact.
• reputed company-In. We're reputed company-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

The reputed company salary range for this position is $200,000-$240,000 per year, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual reputed company bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees' overall well-being. As an equal opportunity employer, reputed company values an inclusive workplace and welcomes applicants of reputed company backgrounds and experiences. reputed company qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability, or any other factors prohibited by law. 30 Acorn Park Drive | Cambridge, MA 02140 | www.parabilismed.com Apply tot his job Apply To this Job