Associate Director of Practice Area - Life Sciences Join Syska Hennessy Group, a global leader in consulting, engineering, and commissioning services, specializing in advanced technical buildings and their essential systems. We are in search of a dynamic, performance-oriented leader to collaborate with our national life sciences and healthcare teams. This role offers the opportunity to oversee and develop our practice area in the Northeast or West region, capitalizing on our established legacy and strong client relationships. In this pivotal position, you will spearhead initiatives to secure and manage pharmaceutical manufacturing, laboratory, and medical device projects. You will oversee the regional life sciences team, guiding the development of strategic business plans and executing a diverse range of projects. This role reports directly to the regional leader of the firm. Our vibrant work environment promotes professional growth, combining a supportive culture, a diverse workforce, competitive compensation, and a flexible work schedule (Monday to Thursday in-office for 9 hours and Friday 4 hours remotely). We also host engaging social events, making it an ideal setting for a fulfilling and challenging career. As a management-owned entity, we are committed to rewarding our key leaders with opportunities for ownership, promoting overall performance and recognition.

Associate Practice Area Director - Healthcare Design Join us at Syska Hennessy Group, a premier global consulting, engineering, and commissioning firm specializing in the creation of advanced technical buildings. We are in search of a dynamic and results-oriented leader to join our global science and technology team. This role offers the exciting potential to lead our healthcare design practice in Los Angeles, CA; San Diego, CA; or San Francisco, CA. Embrace this opportunity to build upon our esteemed legacy and brand while engaging with our diverse client base and innovative projects. Please note, travel will be a part of this role. As the Associate Practice Area Director, you will spearhead the pursuit, winning, and execution of healthcare projects, including but not limited to inpatient hospitals, ambulatory surgery centers, behavioral health facilities, and medical office buildings. You will provide managerial oversight to our regional healthcare team, steering the development of business strategies and executing various projects, organizational structures, and processes. This role will report directly to the regional and practice area leadership within our firm. Our vibrant work environment is designed to elevate your engineering career. With a supportive culture, a diverse workforce, competitive compensation, and a flexible work schedule (Monday to Thursday in-office for 9 hours and Friday for 4 hours remotely), alongside engaging social events, we provide everything you need for a fulfilling and challenging career. As a management-owned private entity, we are dedicated to recognizing and rewarding our key leaders with ownership opportunities that drive overall performance and acknowledgment.

Data Analyst (Life Sciences Specialist) - Direct Hire ($125,000 - $210,000)Highlights:Telecommute from anywhere in the US (West Coast preferred).Become a valued member of a seasoned team of Biotech/Life Sciences specialists known for their market excellence.Specializing in data analysis for Go-to-Market strategies in the Life Sciences sector, covering Operations, Delivery, Distribution Channels, and Market Access.Focus primarily on West Coast clients.Engage in data analysis and strategic projects for prestigious, top-tier Biotech companies.

Join ServiceNow as an Enterprise Account Executive focusing on the Life Sciences sector in beautiful San Diego. In this role, you will develop and nurture relationships with enterprise clients, driving engagement and sales of our innovative solutions tailored for the life sciences industry. You will leverage your industry expertise to understand client needs and articulate the value of our offerings, contributing to their operational efficiency and success.

Join Skyline Construction: Building Better TogetherSkyline Construction, a pioneering leader in the commercial interior construction sector since 1996, is seeking a dedicated Project Manager to join our dynamic team. With multiple offices across California, Washington, and Illinois, we pride ourselves on our employee-owned model and have earned recognition as one of Inc. Magazine’s Best Workplaces for the last five years. At Skyline, we embrace the philosophy of 'building better together' and value collaboration and innovation in every project we undertake.

Join Skyline Construction: Building Better TogetherSkyline Construction, a pioneer in commercial interior construction since 1996, invites you to be part of our dynamic team. With multiple offices across California, Washington, and Illinois, we are proud to be 100% employee-owned. Recognized as one of Inc. Magazine’s Best Workplaces for the past five years, we embody the spirit of collaboration and excellence. At Skyline, we believe that together, we are shaping a better future.

About Acadia Pharmaceuticals Acadia Pharmaceuticals focuses on bringing scientific advances to patients affected by neurological and rare diseases. The company’s commercial portfolio includes the only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. Acadia continues to develop a varied pipeline, with programs in mid- to late-stage development for Alzheimer’s disease psychosis and Lewy body dementia psychosis, along with earlier-stage research addressing additional unmet needs. Location and Hybrid Work This Director of Translational Science Operations position may be based in San Diego, CA; San Francisco, CA; or Princeton, NJ. Acadia’s hybrid work model requires an on-site presence in the office three days per week on average. Role Overview The Director will lead operations for Translational Sciences, supporting nonclinical, toxicology, and pharmacology/pharmacometrics clinical teams. This position manages systems that support both clinical and nonclinical activities within the Translational Science department. Responsibilities include vendor and contract oversight, due diligence on agreements, and managing budgets and timelines. Success in this role depends on effective collaboration with internal and external stakeholders to ensure timely and coordinated execution across Acadia’s programs. Key Responsibilities Oversee operational management of Translational Science project activities, working closely with functional representatives to deliver on plan and within budget.

About Acadia Pharmaceuticals Acadia Pharmaceuticals focuses on turning scientific discoveries into meaningful treatments for underserved communities affected by neurological and rare diseases. The company’s commercial portfolio includes the first and only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. Acadia continues to advance a diverse pipeline, with mid- and late-stage programs for Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as early-stage efforts aimed at additional unmet needs. The team is committed to making a real difference in patients’ lives. Location and Work Model This position may be based in San Diego, CA, San Francisco, CA, or Princeton, NJ. Acadia offers a hybrid work model. Role Overview The Executive Director of Translational Sciences leads the design and execution of disease and drug mechanism of action (MoA) studies that advance therapeutics through clinical development. This position requires deep expertise in translational sciences and hands-on experience in rare diseases. Strong leadership and mentoring skills are essential, as well as a thorough understanding of clinical biomarker development and the full drug development process from discovery through late-stage clinical trials. Success in this role depends on the ability to translate complex biological concepts and data into clear, actionable insights. The Executive Director must also demonstrate a record of effective cross-functional collaboration throughout the drug development process.

Role Overview Acadia Pharmaceuticals is hiring an Associate Director of Clinical Operations. This position is based in either Princeton, New Jersey or San Diego, California. The Associate Director will guide key phases of clinical trials, focusing on high-quality execution and adherence to regulatory requirements. What You Will Do Lead and oversee essential stages of clinical trial operations Ensure all activities meet regulatory and company standards Promote effective collaboration across multiple teams Drive project timelines to support company objectives Take a hands-on approach to managing clinical operations

Join Acadia Pharmaceuticals as the Associate Director of Clinical Data Management, where you will lead and oversee the clinical data management functions critical to our drug development processes. In this pivotal role, you will ensure data integrity, compliance with regulatory standards, and contribute to the generation of high-quality data for our clinical trials.

Fate Therapeutics is seeking a dynamic and experienced Senior Manager or Associate Director of Project Management to become a vital member of our Global Business Operations team. In this pivotal role, you will collaborate closely with the Development and Technical Operations departments to oversee the complete lifecycle of intricate projects. This position acts as a crucial bridge between operational execution, program development strategies, and portfolio direction across our clinical stage programs. This is a full-time, exempt position based at our corporate headquarters in San Diego, CA, reporting directly to the Vice President of Global Operations.

Join Iambic Therapeutics as the Associate Director of Drug Metabolism and Pharmacokinetics (DMPK), where you will drive innovative DMPK strategies throughout our discovery and preclinical development programs. Your expertise will be pivotal in designing and implementing integrated ADME/PK strategies that facilitate program advancement and inform critical decision-making for IND submissions.In this role, you will represent DMPK on cross-functional teams, collaborating closely with our internal scientists and external CRO partners to plan, execute, and interpret studies. This position is based at our San Diego Headquarters, where you will be at the forefront of advancing therapeutic candidates. KEY RESPONSIBILITIESDesign and implement DMPK strategies to propel discovery and development initiatives.Plan, execute, and interpret DMPK studies to support the progression of therapeutic candidates during discovery and early development stages.Collaborate with diverse teams including medicinal chemistry, biology, CMC, and clinical to provide DMPK insights that inform project decisions.Utilize AI-driven tools and computational methods to enhance DMPK strategy, facilitate predictive ADME/PK assessments, and expedite data-driven decision-making.Address ADME/PK-related challenges during lead optimization.Oversee external ADME/PK and PK/PD studies, coordinating with CROs and reviewing data.Prepare DMPK summaries and regulatory submission documentation (e.g., IND, IB).Interpret ADME/PK data, communicating findings and recommendations effectively to project teams.Stay abreast of advancements in DMPK, PBPK, PK/PD, and regulatory guidelines.Ensure that all studies comply with relevant regulatory and quality standards.

Establish and Expand Your ABA Practice with No Upfront Investment!Join the innovative team at 3Y Health and enjoy the flexibility of earning between $100,000 and $320,000 annually while setting your own hours.Are you exhausted by inflexible clinical settings and seeking a way to combat professional burnout? Do you aspire to create your own practice but feel unsure about how to proceed? At 3Y Health, we believe that Board Certified Behavior Analysts (BCBAs) deserve more—more autonomy, more resources, and a greater opportunity to make a significant impact. We offer a unique platform that enables you to launch and cultivate your own ABA practice without any initial costs, accompanied by comprehensive operational support.We manage the logistics, allowing you to concentrate on providing exceptional care.What Sets 3Y Health Apart?No Initial Fees – Join with $0 upfront; no hidden charges.Potential earnings of up to $320,000/year based on your client load and chosen schedule.Dedicated assistance with LLC formation, business banking, and liability insurance.Complete flexibility – Choose your working hours, clients, and therapeutic approach.Top-notch support – We handle the operations so you can focus on achieving clinical excellence.Tailored referral services to help you develop your ideal client base.What We Offer:Comprehensive software package – Encompassing Practice Management, Scheduling, EHR, Data Collection, Billing, Onboarding, and mobile applications for you, your Registered Behavior Technicians (RBTs), and your clients.Insurance collaborations – We are in-network with over 100 payers at competitive rates, ensuring extensive patient access.Support for practice establishment – We’re here to assist you in starting your own ABA company if you haven't yet.Quick payments – Receive rapid payment for each session, eliminating the hassle of insurance claims.Simplified payroll – We can handle payroll for you and your RBTs if desired.Your Responsibilities:Oversee and manage your practice – Determine your working hours, select clients, and decide on your care delivery methods.Recruit and mentor your RBTs – Assemble a team that aligns with your objectives and values.Provide outstanding ABA therapy – You are the specialist; we empower you to excel.

Role Overview Platform Science is seeking a Director of Business Systems to guide the strategy, architecture, and operations of our NetSuite and Salesforce environments. This leadership position reports to the VP of IT and can be based remotely within the Pacific Time Zone or in San Diego, CA. About Platform Science Founded in 2015, Platform Science builds an open IoT platform for the transportation industry. Our teams work alongside fleets, application developers, vehicle manufacturers, and equipment providers to deliver solutions that help supply chain professionals worldwide. We value diverse perspectives, empathy, and transparent collaboration across all roles. What You Will Do Lead the global NetSuite and Salesforce ecosystems, setting vision and strategy for these platforms. Oversee systems architecture and drive process improvements across business functions. Manage the full lifecycle of business systems, from planning through administration and optimization. Supervise and mentor a distributed team of administrators and analysts. Act as subject matter expert for NetSuite and Salesforce, especially in the Lead-to-Cash process. Oversee related systems and processes, including CPQ, CLM, AR/AP automation, PLM, and billing. Collaborate with executive stakeholders to align technology initiatives with business goals. Location This role is open to candidates in the Pacific Time Zone, with the option to work remotely or from our San Diego, CA office.

Join Amgen as a Medical Science Liaison specializing in Cardiovascular medicine in San Diego. In this pivotal role, you will be the bridge between our innovative research and the medical community, providing expert knowledge and support to healthcare professionals.

Role overview Saalex Solutions, Inc. seeks a Life Cycle Management Analyst I in San Diego, California. This entry-level analyst helps support clients throughout different stages of product life cycles. The role involves data analysis, process improvement, and contributing to solutions that adapt to customer needs. What you will do Analyze data related to product life cycles Identify ways to improve existing processes Support teams to ensure solutions align with changing customer requirements Growth and development This position offers opportunities to learn and build skills while working alongside experienced colleagues.

We are seeking a highly motivated and detail-oriented Research Associate III to join our dynamic team in San Diego. In this role, you will be responsible for conducting advanced research in a collaborative environment, contributing to innovative projects, and supporting our overarching goals. You will work closely with senior researchers and cross-functional teams to ensure the successful execution of research initiatives.

Veeva Systems is a pioneering enterprise dedicated to transforming the life sciences industry through innovative cloud solutions, enabling companies to expedite the delivery of therapies to patients. As a rapidly expanding SaaS leader, we achieved over $3 billion in revenue last fiscal year, with promising growth on the horizon. At Veeva, our core values shape our culture: Doing the Right Thing, Ensuring Customer Success, Supporting Employee Success, and Emphasizing Speed. We distinguish ourselves from other public companies by our commitment to being a public benefit corporation (PBC), which legally obligates us to balance the interests of our customers, employees, society, and investors. As a Work Anywhere organization, we offer the flexibility to work from home or in the office, empowering you to excel in your preferred environment. Join us in our mission to revolutionize the life sciences sector, making a meaningful impact on our customers, employees, and communities.The RoleWe are seeking an accomplished Account Partner to lead sales initiatives within our Commercial Practice. In this pivotal role, you will synchronize customer goals with our Commercial Cloud platform, leveraging effective communication across various business functions and organizational levels, including C-suite executives. A blend of creativity, proactivity, and the ability to collaborate within a growing team will be essential for your success. This prominent position demands extensive industry knowledge and expertise. You will work closely with clients to grasp their Commercial operations requirements and align Veeva's products and services accordingly to ensure customer success.

Hello there!We appreciate your interest in the Medical Science Liaison (MSL) position. Please take a moment to review the details below. If you believe this opportunity aligns with your career aspirations, we encourage you to discuss it with your current manager and HR business partner. If everything checks out, we look forward to receiving your application, and our Talent Acquisition team will be in touch for an interview to get to know you better.- Your Human Resources TeamAbout the RoleThe Medical Science Liaison (MSL) serves under the guidance of our National Director of Field Medical and acts as a vital link between our organization and the healthcare community. MSLs are field-based professionals who engage in compliant scientific dialogue and provide comprehensive education on disease states while addressing inquiries related to our products.Key Responsibilities:Engage with key opinion leaders (KOLs) in optometry and ophthalmology within your designated region while ensuring compliance with PhRMA and Tarsus guidelines.Act as the primary medical affairs KOL contact for daily inquiries and scientific exchanges, utilizing both virtual and in-person interactions.Gather actionable insights from scientific exchanges and prioritize these insights to inform our medical strategy.Deliver comprehensive practice education to optometric and ophthalmic centers.Provide educational resources to Optometry schools and Ophthalmology residency programs.Guide customers on investigator-initiated trial procedures and medical information protocols as needed.Compliantly identify and recommend KOLs for various initiatives including advisory boards, medical education projects, and clinical trials based on their expertise and competencies.Plan KOL engagements and participate in scientific sessions at local, regional, and national medical meetings.Collaborate with local and regional optometric and ophthalmic medical societies.Present scientific evidence to the payer community.Lead and provide expertise on medical affairs initiatives and projects.Engage in continuous improvement of training and field medical processes.Facilitate local disease state scientific exchanges and conduct “lid+lash labs.”Participate in compliant and collaborative engagements with cross-functional teams.