Senior Director, Information Technology Salary at Linkedin Corp BETA

Director/Senior Director, Pharmacovigilance Operations *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 Operations to join their team. Key Responsibilities Review individual and aggregate adverse event reports for potential PV/Drug Safety issues. Ensure that AEs from spontaneous reports, solicited reports, and literature cases involving company products are collected, analyzed, and handled in accordance with all global/local regulatory requirements and company policies. Manage PV vendors to ensure compliance and effectiveness. Serve as an SME for processing ICSR's for clinical-stage programs and commercial products. Collaborate with, and provide PV guidance and support for interdepartmental or corporate initiatives. Key Qualifications BS required, advanced degree preferred (PharmD, PhD) 10+ years of direct experience in PV/Drug Safety Stro

Director/Senior Director, Pharmacovigilance Operations *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 Operations to join their team. Key Responsibilities Review individual and aggregate adverse event reports for potential PV/Drug Safety issues. Ensure that AEs from spontaneous reports, solicited reports, and literature cases involving company products are collected, analyzed, and handled in accordance with all global/local regulatory requirements and company policies. Manage PV vendors to ensure compliance and effectiveness. Serve as an SME for processing ICSR's for clinical-stage programs and commercial products. Collaborate with, and provide PV guidance and support for interdepartmental or corporate initiatives. Key Qualifications BS required, advanced degree preferred (PharmD, PhD) 10+ years of direct experience in PV/Drug Safety Stro

Director/Senior Director, Pharmacovigilance Operations *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 Operations to join their team. Key Responsibilities Review individual and aggregate adverse event reports for potential PV/Drug Safety issues. Ensure that AEs from spontaneous reports, solicited reports, and literature cases involving company products are collected, analyzed, and handled in accordance with all global/local regulatory requirements and company policies. Manage PV vendors to ensure compliance and effectiveness. Serve as an SME for processing ICSR's for clinical-stage programs and commercial products. Collaborate with, and provide PV guidance and support for interdepartmental or corporate initiatives. Key Qualifications BS required, advanced degree preferred (PharmD, PhD) 10+ years of direct experience in PV/Drug Safety Stro

This role will serve as an expert Medical Writer who is responsible for planning, developing, and writing clinical documents to support medical and regulatory activities across the portfolio by ensuring that scientifically robust messages and arguments are developed and conveyed consistently across documents. Responsibilities Apply expert medical writing proficiency to lead the planning and authoring of complex, strategic clinical and regulatory documents and submission packages. Serve as a document planning and writing expert; responsible for guiding a medical writing and project team during the planning and authoring stages across all document types and regulatory submissions, including facilitating document contributor/review meetings, developing and managing timelines, coordinating document review, and driving decision-making. Initiate and drive strategic medical writing initiatives and processes with high technical acumen to ensure execution on company priorities. Lead, and active

About the Company My client is a leading provider of system IP for the acceleration of system-on-chip (SoC) development across today’s electronic systems. Their network-on-chip (NoC) interconnect IP and SoC integration automation technology enable higher product performance with lower power consumption and faster time to market, delivering better SoC economics so its customers can focus on dreaming up what comes next. With over 250 employees with headquarters in Silicon Valley and offices around the globe, they are a catalyst for SoC innovation, so companies ranging from startups to the biggest technology market leaders can effectively create new products with proven connectivity flexibility and ease. About the Role As a Senior Director, Strategic Account Sales, you are a dynamic and experienced Executive Account Manager with a proven track record selling large transaction strategic accounts. With over 8 years of experience, you possess strong business development skills and have a his

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

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

Senior Director, Biostatistics Location: South San Francisco, CA (On-site, 4 days/week) Compensation: ~$300K base + bonus + stock options Type: Full-time About the Role Our client, a clinical-stage precision oncology biotech, is searching for a Senior Director of Biostatistics to lead the Biometrics function and support the development of novel oncology therapeutics. The company is well-capitalized (over $1B in cash), with multiple programs under internal control, and strong momentum including recent Fast Track designation. You’ll work in a high-performance, highly collaborative environment with a strong succession track—this is a strategic leadership role with future elevation potential. The position reports into a leader who is respected, focused, and known for execution excellence. Key Responsibilities Serve as Biostatistics lead for development programs across all clinical phases. Oversee internal/external teams and ensure quality statistical deliverables. Contribute to protocols,