19 Pharmaceuticals jobs in South San Francisco

• We are seeking an SAP Project Manager for the USA West Coast (100% Allocation).
• This position require the GMP experience to lead and manage complex M&A Integration projects.
• You will be responsible for delivering large-scale projects focused on M&A integration with tasks including Project Planning, Concept, Tracking, Reporting, Budget Oversight, Vendor Relationship Management.
• These activities will be within the pharmaceutical industry, and you will lead mid- to large-sized teams, taking full ownership of the project lifecycle to ensure projects are delivered on time, within scope, and within budget while meeting business objectives.

• Lead cross-functional teams across multiple departments, ensuring timely completion of project tasks and driving alignment among stakeholders.
• Develop and manage detailed project plans, covering scope, timelines, resource allocation, and budget.
• Oversee the full lifecycle of M&A integration projects within the remit of the role.
• Facilitate regular meetings, provide consistent status updates, and maintain clear communication across all organizational levels.
• Identify and mitigate risks, ensuring all project deliverables meet or exceed quality standards.
• Maintain detailed project documentation, ensuring adherence to organizational standards and GMP regulations , and lead post-project reviews to drive continuous improvement.
• Onsite travel to the West Coast is planned up to 20%.

• 6-10 years of experience managing M&A integration projects, with at least 3 projects in the pharmaceutical industry.
• Strong understanding of SAP Systems and GMP Compliance.
• Proven leadership skills in managing complex, large-scale projects and cross-functional teams.
• Excellent communication skills.
• Demonstrated ability to identify, escalate, and mitigate risks in high-complexity projects .
• Proficiency in project management tools, with the ability to quickly adapt to specialized industry software.
• PMP certification preferred, educational background in business, IT, or related fields.
• Fluency in English.

Join to apply for the Senior Project Manager / Program Manager, Pharmaceuticals role at IPM Integrated Project Management Company .

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For more than three decades, premier organizations have trusted IPM to lead the successful execution of their strategic portfolios and critically important initiatives. Headquartered in Chicago with offices in Boston, Parsippany, Minneapolis, St. Louis, Los Angeles, and San Francisco, IPM has led more than 5,000 projects for over 500 clients, including Fortune 100 companies and start-ups.

We are a certified Great Place to Work company and have been named to the Great Place to Work list of Best Workplaces in Consulting and Professional Services.

Our Senior Project Management Consultants are our full-time employees and our key differentiator.

IPM partners with clients across the life sciences industry sectors, including pharmaceuticals, medical technology, and biotechnology, covering areas like large-molecule proteins, monoclonal antibodies, cell, tissue, and genetic therapies, and molecularly engineered vaccines.

• We lead product development projects from pre-clinical R&D through commercialization, including regulatory, clinical, and commercial strategies and processes, as well as product lifecycle management.
• We improve operational processes, harmonize regulatory and quality systems, and build project, program, and portfolio management capabilities.

Job Description

As a Senior Project Management Consultant, you will partner with client leadership and delivery teams to lead project and program planning and execution across various functions, driving projects and programs to achieve critical outcomes for our pharmaceutical industry clients . You will gain diverse experience working with different clients and project types.

Your primary goals include:

• Leading product development projects and programs in the pharmaceutical industry, including pre-clinical R&D, commercialization, and product lifecycle management.
• Leading business process development and optimization to enhance project and portfolio management capabilities.
• Developing and executing integrated project plans aligned with strategic objectives.
• Managing projects within scope, schedule, and budget, exceeding IPM standards.
• Formulating high-level strategies to meet project objectives.
• Building and leading high-performance project teams, advocating for the project within the client organization.
• Providing oversight to IPM consultants as needed.
• Contributing to business development through relationship building.
• Participating in IPMs Center of Excellence (CoE).
• Supporting content marketing, proposals, and project activities.
• Engaging in professional development and internal initiatives.

Desired Skills And Experience

The ideal candidate will have:

• A bachelors degree in science, engineering, or a related field; advanced degrees are a plus.
• At least 12 years of experience in the pharmaceutical industry related to IPMs offerings, with 7 years of project management experience, or 20+ years of life sciences experience with at least 2 years in project management.
• Knowledge of disciplined project management processes (Six Sigma, PMP certifications are a plus).
• Exceptional interpersonal and leadership skills for effective communication at all organizational levels.

IPMs Business Offerings include:

• Product development across the full product lifecycle: pre-clinical R&D, clinical development, regulatory submissions, commercialization, product management, quality assurance, and control.
• Business process development and optimization: establishing enterprise or functional project and portfolio management capabilities, improving processes for growth and efficiency.

Why IPM?

• Engaging culture with transparent communication and team-building events.
• Commitment to diversity, equity, and inclusion.
• Opportunities for professional growth and internal promotion.
• Exposure to diverse projects and clients.
• Supportive, collaborative environment with Centers of Excellence.
• Comprehensive benefits, including health coverage, 401(k), bonuses, and more. Salary range: $155,000 - $200,000.
• Community involvement through initiatives like Project Mercy.

Note: Salary estimates are based on experience and market conditions.

IPM is an equal opportunity employer, committed to diversity and inclusion.

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Project Management
• Industries: Business Consulting and Services

• Lead and manage multiple drug discovery research projects from inception to completion.
• Design, optimize, and validate in vitro and in vivo experimental assays.
• Analyze and interpret complex biological and chemical data to draw meaningful conclusions.
• Contribute to the identification and validation of novel drug targets.
• Conduct hit-to-lead and lead optimization studies in collaboration with medicinal chemistry.
• Prepare comprehensive research reports, scientific presentations, and manuscripts for publication.
• Stay abreast of the latest scientific literature and technological advancements in the field.
• Collaborate effectively with internal teams and external partners.
• Mentor and guide junior research scientists and technicians.
• Ensure adherence to all relevant laboratory safety protocols and regulatory guidelines.

• Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
• 8+ years of progressive experience in pharmaceutical drug discovery and development.
• Demonstrated expertise in leading research teams and managing complex R&D projects.
• Proven track record of successful target identification, validation, and lead optimization.
• Extensive experience with in vitro and in vivo pharmacology models.
• Proficiency in data analysis software and bioinformatics tools.
• Excellent scientific communication and presentation skills.
• Familiarity with GMP/GLP principles and drug development regulatory pathways.
• Ability to thrive in a fast-paced, innovative research environment.

• Design, execute, and interpret complex experiments to identify and validate novel drug targets in oncology.
• Develop and optimize cell-based and biochemical assays for drug screening and characterization.
• Conduct pre-clinical studies, including *in vitro* and *in vivo* efficacy models.
• Analyze and present experimental data to research teams, project leaders, and senior management.
• Collaborate with cross-functional teams, including medicinal chemistry, pharmacology, and DMPK.
• Contribute to the writing of research reports, publications, and patent applications.
• Maintain a high level of scientific rigor and contribute to a culture of innovation.

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• Design and execute complex biological experiments to identify and validate novel drug targets.
• Develop and optimize in vitro and in vivo preclinical models to assess drug efficacy and safety.
• Characterize the pharmacological properties of drug candidates, including mechanism of action studies.
• Analyze and interpret experimental data, troubleshoot experiments, and present findings at scientific meetings and internal reviews.
• Write detailed research reports, contribute to regulatory submissions, and prepare manuscripts for publication.
• Collaborate with medicinal chemists, pharmacologists, toxicologists, and clinical development teams.
• Stay abreast of the latest scientific advancements and emerging technologies in the pharmaceutical industry.
• Mentor and guide junior research scientists and research associates.
• Manage external collaborations with academic institutions and contract research organizations (CROs).
• Contribute to the strategic direction of the R&D pipeline.