Director, Vendor Management Salary at Tilia Inc BETA

We are actively searching for a full-time Senior Project Manager in the SF/Bay Studio. Our incredible team works diligently & closely with our clients to realize goals, ideas, brand and culture into powerful, engaging workplaces. IA’s diverse, global client roster requires high-performance, inventive, visually compelling, adaptable and sustainable solutions moving their enterprise forward, support their culture, engage their staff, and integrate ever-changing technology. Our team members are creative-thinkers, experts, collaborative, passionate and professional. Joining our team requires equally passionate thought leaders, conceptual thinkers with a willingness to experiment, learn and teach our clients, consultants, and employees…all while having fun and a love of workplace interiors. This role assumes full responsibility for procuring, planning, staffing, coordinating, and administering projects. As a “seller-doer” your specific responsibilities include, but are not limited to: Ident

Senior Project Manager/Associate Director, Project Management About Us: Timberlyne Therapeutics is a clinical-stage biopharmaceutical company focused on the development and commercialization of transformational therapies for high unmet medical needs. Timberlyne’s lead program is CM313, an IgG1 monoclonal antibody with enhanced complement-dependent cytotoxicity that targets CD38. By targeting CD38, which is highly expressed on plasma cells, NK cells, and other immune cells, CM313 modulates multiple immune cell types leading to both rapid and durable responses across a range of autoimmune diseases and cancers. Position Summary: We are seeking a skilled and dynamic Senior Project Manager (PM) or Associate Director (AD) of Project Management to lead and support cross-functional teams to drive the successful execution of projects within Timberlyne’s portfolio/pipeline. S/he ensures timely delivery of clinical trials, drug development, or other R&D projects, aligning with company goals and r

Senior Manager/Director, Project Management CMC About Us: Timberlyne Therapeutics is a clinical-stage biopharmaceutical company focused on the development and commercialization of transformational therapies for high unmet medical needs. Timberlyne’s lead program is CM313, an IgG1 monoclonal antibody with enhanced complement-dependent cytotoxicity that targets CD38. By targeting CD38, which is highly expressed on plasma cells, NK cells, and other immune cells, CM313 modulates multiple immune cell types leading to both rapid and durable responses across a range of autoimmune diseases and cancers. Position Summary: Timberlyne is seeking a Project Manager, CMC responsible for successful delivery of large scale, complex CMC projects, and programs with senior-level internal and/or external stakeholders and vendors within approved budget, schedule, scope, and quality standards. This person will be responsible for overseeing project delivery resources to ensure the use of standardized project

Director/Senior Director, Analytical Development and Formulation About Us: Timberlyne Therapeutics is a clinical-stage biopharmaceutical company focused on the development and commercialization of transformational therapies for high unmet medical needs. Timberlyne’s lead program is CM313, an IgG1 monoclonal antibody with enhanced complement-dependent cytotoxicity that targets CD38. By targeting CD38, which is highly expressed on plasma cells, NK cells, and other immune cells, CM313 modulates multiple immune cell types leading to both rapid and durable responses across a range of autoimmune diseases and cancers. Position Summary: Timberlyne is searching for a Director of Analytical Development and Formulation. The position will contribute to the formulation, drug product development and GMP drug product manufacturing for Timberlyne’s large molecule clinical pipeline. The successful candidate will manage and collaborate with contract development and manufacturing vendors and ensure timel

Senior Director of Pharmacovigilance (PV) – Summary: Company Overview: Clinical-stage biopharmaceutical company focused on rare diseases. Located in the San Francisco Bay Area, CA. Key Responsibilities: Evaluate and assess adverse event (AE) reports for safety issues. Manage PV vendors and ensure compliance. Act as Subject Matter Expert (SME) for Individual Case Safety Report (ICSR) processing. Ensure AE reporting complies with global regulations (FDA, EMA, ICH). Update and create SOPs; lead process improvement initiatives. Collaborate with departments and partners on drug safety data exchange. Lead training on AE and product complaints for internal teams and vendors. Qualifications: Education: Bachelor’s in science/health-related field; advanced degrees are a plus. Experience: 10+ years in Pharmacovigilance, Drug Safety, or Risk Management. Knowledge: Strong understanding of global PV regulations (e.g., US CFR, EMA, ICH). Technical Skills: Proficiency with safety databases (e.g., Orac

This is a CONFIDENTIAL job opportunity for a CLIENT of Guide to HR. This is NOT a job for Guide to HR. About the Client who is hiring: B2B AI Tech VC backed Global What You’ll Do Reporting to the Marketing Department Head, this high-impact, hands-on leadership role is responsible for owning and scaling our global demand generation engine. You’ll lead the strategy and execution of full-funnel marketing programs that drive predictable, scalable pipeline — partnering closely with sales, product marketing, and RevOps. You’ve done this before. You’ve taken a company from Series B or C to $100M+ in ARR, building high-performing demand engines using a mix of inbound, outbound, ABM, and lifecycle strategies. You're data-driven, revenue-obsessed, and deeply fluent in HubSpot. Key Responsibilities: Own the pipeline. Drive strategy, execution, and reporting across all demand channels to generate and accelerate qualified pipeline growth. Lead the function. Build, mentor, and scale a high-performin

Job Description Job Description Position Summary The Director, Technology will lead the transformation of an evolving service organization. Operating on the macro and micro levels, as a leader championing change, you will develop and steer a roadmap to drive continued operational initiatives and partner with Programs and other agency functions (HR, Finance, Recruiting, Training) to deliver scalable solutions through continuous improvement approaches. You will oversee IT and Facilities systems and projects, data analysis, business intelligence, telecommunication systems, Internet and intranet, and technical and operational support for staff. The successful candidate is deeply service minded, a project management expert, obsessed with support and troubleshooting; and a natural leader with the persuasiveness to drive technological advancements of an organization with a large field contingency (80% of 500+ person staff). Essential Job Functions Lead and manage network/helpdesk staff, busin

Director, Pharmacovigilance *Hybrid Opportunity (2-3x per week onsite in Redwood City, CA)* Meet has partnered with an exciting biotech in the rare disease space that is looking for a Director of Pharmacovigilance/Drug Safety to join their team. Key Responsibilities Review individual and aggregate adverse event reports for potential PV/Drug Safety issues Manage PV vendors to ensure compliance and effectiveness Serve as an SME for processing ICSR's for clinical-stage programs and commercial products Key Qualifications BS required, advanced degree preferred (PharmD, PhD) 10+ years of direct experience in PV/Drug Safety Strong understanding of US and EU PV guidelines Please reach out if you're interested in learning more: ✉: ryan.moran@meetlifesciences.com