Senior Clinical Trial Associate

At Olema Oncology, we are committed to advancing innovative treatments for breast cancer and beyond. Our flagship program, palazestrant (OP-1250), represents a pioneering complete estrogen receptor antagonist (CERAN) currently under investigation for metastatic breast cancer, with significant potential both as a standalone therapy and in combination with existing treatments for ER+/HER2- metastatic breast cancer. Furthermore, our subsequent candidate, OP-3136, is a promising KAT6 inhibitor expected to set new standards in efficacy.We foster an environment of scientific excellence through unwavering support, motivation, and constructive challenges among our team members. At Olema, prioritizing our people ensures our work stands out in the industry. If you are prepared to embark on an exciting journey with us and make a meaningful difference for our patients, your career, and the future of medicine, we want to hear from you.Explore our latest corporate presentations here.About the Position: Senior Clinical Trial AssociateAs a Senior Clinical Trial Associate, you will report directly to the Senior Manager, Clinical Trial Leader, and provide essential administrative and operational support to our clinical teams throughout all phases of the study lifecycle, including both in-house and outsourced trials. Your role will facilitate seamless study execution through collaboration with internal teams, external vendors, and site personnel. This includes contributing to essential study documentation such as informed consent forms (ICFs) and central IRB submissions, managing site payments, and overseeing various operational tasks related to the study. You will also serve as a liaison to investigator sites, ensuring effective communication and follow-up.Your responsibilities will encompass assisting with study initiation, maintenance, and closure activities; managing study documentation and materials; supporting vendor management; and maintaining accurate study trackers and financial records. This role adheres strictly to Clinical Standard Operating Procedures and Good Clinical Practice (ICH) guidelines.This position is available in either our San Francisco or Cambridge office and will require approximately 10% travel.Your core responsibilities include:Supporting the Clinical Trial Lead (CTL) and Study Execution Team (SET) by ensuring accurate and comprehensive documentation of study conduct.Managing study-related vendors and acting as the primary contact for contracted CROs, study personnel, contract laboratories, and other relevant vendors.Being a key point of contact for investigator sites...

Join our dynamic team as a Senior Clinical Trial Manager in San Francisco! In this pivotal role, you will oversee and manage clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data integrity. This is an exciting opportunity for professionals who are passionate about advancing medical research and improving patient outcomes.

At Precision for Medicine, we are a dedicated team of clinical trial professionals committed to facilitating the advancement of medical treatments for patients in need. From our inception, we have fostered a culture that prioritizes the needs of patients and clients alike, ensuring the highest quality of work while allowing our employees to thrive in a fun and supportive environment. Join our Clinical Trial Management team and contribute to meaningful healthcare solutions that save and enhance lives every day!In this role, you will take charge of leading and managing the clinical team throughout the study, focusing on adhering to timelines and project scopes while ensuring quality outcomes. We seek passionate, energetic professionals who relish challenges, pay attention to detail, and thrive in dynamic settings. If you excel at fostering effective partnerships and are committed to delivering exceptional results, we invite you to explore this opportunity with us.

Join us in our mission to enhance health equity by improving access to cancer precision medicine.About Trial LibraryFounded in 2022, Trial Library, Inc. is a dynamic, venture-backed startup committed to revolutionizing clinical trial enrollment and retention through our innovative AI platform. As a dedicated health technology company, our primary goal is to bridge the gap in cancer care by providing greater access to precision medicine via clinical trials. We collaborate closely with community oncology sites, patients, and industry partners to make clinical research accessible, understandable, and inclusive for all.In the role of Ally Navigator, you will play a pivotal role in supporting cancer patients and their caregivers by guiding them through the process of discovering clinical trials as a viable treatment option. You will serve as their initial point of contact, ensuring they receive the assistance they need during what can be a challenging and vulnerable time. Success in this position requires a deep understanding of clinical research, along with the ability to convey complex information effectively to individuals with varying backgrounds and levels of health literacy.

Join HeartFlow, a pioneering medical technology firm dedicated to enhancing the diagnosis and management of coronary artery disease—the leading cause of death globally—through innovative technology. Our flagship product, the HeartFlow FFRCT Analysis, utilizes AI to deliver a non-invasive cardiac test that provides a detailed, color-coded 3D model of a patient's coronary arteries, illustrating the influence of blockages on heart blood flow. HeartFlow leads the way as the first AI-driven, non-invasive integrated heart care solution across the CCTA pathway, assisting clinicians in identifying coronary artery stenoses (via RoadMap™ Analysis), evaluating coronary blood flow (through FFRCT Analysis), and analyzing coronary atherosclerosis (with Plaque Analysis). As our product pipeline expands, so does our team—join us in the quest to revolutionize precision heart care.HeartFlow is a publicly traded company (HTFL) recognized globally for its remarkable contributions to healthcare innovation. Supported by medical societies worldwide and cleared for use in the US, UK, Europe, Japan, and Canada, our solutions have benefitted over 500,000 patients globally.The Clinical Trial Manager (CTM) will oversee and coordinate all clinical operations at the trial and site level. This role requires effective collaboration with the HeartFlow Clinical Research team, site staff, clinical research coordinators, principal investigators, and vendors to ensure that clinical studies are executed on time and uphold high-quality standards. The ideal candidate will bring proven experience in clinical research study execution, outstanding organizational abilities, meticulous attention to detail, and a capability to thrive in a dynamic startup environment.

Join AbbVie, a global biopharmaceutical company, as a Clinical Research Associate II in the vibrant Bay Area. In this critical role, you will be responsible for overseeing clinical trials, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to bring innovative therapies to patients.

General Manager/CEO, Clinical Trial Abundance InitiativeLocation: Remote (US-Based) | Type: Full-Time | Reports to: CEO, Philanthropic FoundationEQL Tech is collaborating with two philanthropic foundations on an ambitious initiative to transform the clinical trial landscape. Our mission is to ensure that revolutionary therapies are delivered to patients quickly and fairly. We are dedicated to dismantling systemic barriers that hinder access and diversity in clinical trials, striving to enhance the representation of clinical trial participants and amplify the efficacy of innovative health solutions.Role OverviewThe foundation is in search of a General Manager/CEO for the new Clinical Trial Abundance Initiative. In this pivotal role, you will spearhead efforts to decentralize clinical trial access, focusing on patient-centered approaches and fostering diverse participation. You will be responsible for formulating and executing strategies that enable health systems, community groups, and patients to engage more actively in the clinical trial process.Key ResponsibilitiesDevelop and implement strategies to enhance clinical trial accessibility, especially for underrepresented communities.Partner with health systems, patient advocacy organizations, and research institutions to optimize participation pathways and disseminate effective outreach practices.Incorporate community engagement and ecosystem development strategies into clinical trial planning and execution, ensuring trials mirror real-world patient diversity.Advocate for policy reforms at local, state, and federal levels to increase regulatory flexibility in clinical trial designs.Track and assess the progress of the initiative, adapting strategies based on data-driven insights and stakeholder feedback.Collaborate with thought leaders and experts to promote innovative practices that reshape the clinical trial framework.

Join Tyson & Mendes – Senior Counsel, Complex Trial TeamsWhere Insurance Defense Meets InnovationPlease note: An active bar license in the State of California is required.At Tyson & Mendes, we are not just litigators—we are leaders. As a prominent national firm in insurance defense and trial advocacy, we are renowned for our ambitious mission to combat Nuclear Verdicts® and our results-driven approach to high-stakes litigation. We are expanding our Complex Trial Teams and are on the lookout for skilled Senior Counsel who are eager to make a significant impact in the courtroom and beyond.If you are a seasoned trial attorney who excels in navigating complex, high-stakes cases, values thoughtful strategy over mere spectacle, and wishes to be part of a team that is transforming the landscape of civil defense—this is your moment to shine.

Trial Attorney – Criminal Defense | Michael & Associates, San Francisco, CAAt Michael & Associates, we are revolutionizing criminal defense in California. Following our remarkable successes in Texas, we’re bringing our innovative strategies and exceptional client service to San Francisco and the surrounding areas.Our ambitious mission is to become the nation's largest and most effective criminal defense firm within the next three years while fostering an environment where our attorneys can thrive both personally and professionally, ensuring that every client receives unparalleled advocacy and premium service.What Sets Us ApartWe’re redefining the conventional defense firm model by integrating excellent courtroom advocacy with cutting-edge technology. Our use of digital marketing, automation, and data-driven recruitment strategies allows us to extend our reach, enhance outcomes, and cultivate a progressive legal organization.About the PositionWe are on the lookout for a highly experienced Trial Attorney with a stellar reputation in San Francisco's criminal courts. The ideal candidate will command respect in the courtroom, effectively communicate with juries, and be passionately dedicated to defending the rights of the accused.In this pivotal role, you will manage complex criminal cases from arraignment through to trial, supported by a talented team of attorneys, investigators, and support staff. This is an extraordinary chance to make a significant impact on the future of criminal defense in California.Why This Opportunity is UniqueLaunch Your Career at a Rapidly Growing FirmJoin us at the forefront of change and contribute to building something remarkable. Your contributions will be impactful from day one.Defined Growth and Leadership OpportunitiesWe provide unique advancement pathways within the criminal defense sphere. Whether you aspire to lead, refine your trial skills, or mentor colleagues, a clear career trajectory awaits you.Innovation That Drives Your SuccessWe utilize technology, efficiency, and ongoing improvement not just as buzzwords, but as essential tools that enable you to focus on what truly matters: providing outstanding legal service to your clients.A Supportive Team EnvironmentCollaboration is the cornerstone of our practice. Our attorneys challenge, support, and uplift one another to achieve the highest levels of legal excellence.Make a Significant Impact DailyAssist clients through their most challenging times and deliver results that truly matter. Our firm is recognized for combining passionate advocacy with compassion and professionalism.

Our Mission and VisionAt Unlearn, we are on a transformative journey to revolutionize clinical development, making every clinical trial smarter and more efficient. Leveraging the power of data, artificial intelligence, and digital twins, we enable rapid and robust studies that expedite the delivery of life-saving treatments to patients. Our commitment to this mission shapes every facet of our partnerships with biopharmaceutical companies, as we redefine how clinical trials are conceptualized, executed, and analyzed.We are at the forefront of clinical development, instilling unmatched scientific credibility and replacing uncertainty with AI-driven precision. This clarity empowers stronger decision-making and enhances trial efficacy. Our goal is not just to disrupt the pharmaceutical sector; we aim to create meaningful and lasting change.We firmly believe that AI will shape the future of medicine, and we are dedicated to building this future responsibly, rigorously, and in collaboration with our clinical development partners.About Our TeamOur diverse team hails from various backgrounds, including machine learning, marketing, and more. Regardless of our origins, all Unlearners embody common traits:Ambition: We embrace big, challenging goals without hesitation.Disciplined Experimentation: We decompose our large objectives into manageable tasks, meeting frequently to monitor progress and adapt swiftly.Resilience: Setbacks motivate us to strive harder, as we never back down.Openness to Innovation: We resist complacency and thrive on new ideas.Effective Communication: Sharing knowledge is crucial, and we aim to make our interactions engaging.Team Orientation: We prioritize our mission first, the company second, the team third, and individual goals last.Founded in 2017 and headquartered in San Francisco, Unlearn has garnered investment from leading venture firms like Altimeter, Insight Partners, Radical Ventures, 8VC, DCVC, and DCVC Bio, successfully closing our $50 million Series C funding round in January 2024.If our mission and culture resonate with you, we encourage you to apply.

Tyson & Mendes LLP seeks a Senior Counsel for its Complex Trial Teams in San Francisco, CA. This position is designed for experienced trial attorneys with a strong background in insurance defense and high-stakes litigation. Role overview Senior Counsel will join a team known for its leadership in insurance defense and trial advocacy. The focus is on handling complex cases, including those with significant exposure and challenging legal issues. Tyson & Mendes is recognized for its work in combating Nuclear Verdicts® and for delivering results in demanding courtroom settings. What you will do Lead and manage complex, high-stakes trials as part of a collaborative team Develop and execute litigation strategies that emphasize substance and results Play a central role in redefining civil defense approaches within the firm Requirements Active bar license in the State of California (required) Significant experience as a trial attorney, especially with complex litigation and insurance defense Proven ability to navigate high-stakes cases with a strategic mindset This role is ideal for attorneys who value thoughtful strategy over theatrics and want to make a meaningful impact in civil defense.

Join Lewis Associates as a Litigation and Trial Practice Attorney in the vibrant city of San Francisco. In this role, you will be responsible for representing clients in various litigation matters, preparing legal documents, and advocating on their behalf in court. Your expertise in trial practice will be crucial as you navigate complex legal challenges.

At Olema Oncology, we are committed to pioneering advancements in breast cancer treatment and beyond. Our flagship program, palazestrant (OP-1250), serves as a complete estrogen receptor antagonist (CERAN) currently advancing through development for metastatic breast cancer, showcasing immense potential both as a standalone treatment and in synergy with other therapies for ER+/HER2- metastatic breast cancer. Additionally, we are excited about our follow-on candidate, OP-3136, a powerful KAT6 inhibitor that aims to set new benchmarks in its class.Our culture thrives on bold scientific innovations, driven by a supportive, motivating, and challenging environment. At Olema, we believe that prioritizing our people leads to unparalleled outcomes in our work. If you are eager to be part of an unstoppable force in advancing healthcare, let’s collaborate to make a significant impact for our patients, your career, and the future.To explore our latest corporate materials, including our corporate deck and presentations, click here.About the Role: Associate Director of Clinical Supply ChainIn the role of Associate Director of Clinical Supply Chain, reporting directly to the Senior Director, you will be responsible for the strategic planning, creation, implementation, and optimization of our clinical supply chain to guarantee a seamless and timely drug supply for Olema's clinical programs. The position is based in either our San Francisco or Cambridge office and may require approximately 15% travel, both domestic and international.Your primary responsibilities will include:Comprehensive management of the clinical supply chain from end to end.Development and execution of global Clinical Supply Chain strategies.Management of global inventories, shipping logistics, and coordination with third-party manufacturers.Development and oversight of Interactive Response Technologies (IRT) systems.Supervision of packaging, labeling, and distribution across multiple vendors.Creation and management of clinical labels.Identification and escalation of supply chain risks and resolution of risk items.Collaboration with Clinical Operations to align on assumptions and build clinical supply to meet program demands.Representation of the Clinical Supply Chain on study execution teams.

Join Acadia Pharmaceuticals as the Associate Director of TMF Management & Inspection Readiness. In this pivotal role, you will spearhead the management of the Trial Master File (TMF) and ensure inspection readiness across various clinical trials. Your expertise will contribute to the successful execution of our clinical programs, maintaining high standards of compliance and quality.

Join Abridge as the Senior Director of Clinical Success, where you will play a pivotal role in enhancing patient care through innovative healthcare solutions. You will lead a dynamic team, collaborating closely with clinical and operational stakeholders to ensure the effective delivery of our services. Your strategic vision and leadership will drive the success of our clinical programs, making a meaningful impact on patient outcomes.In this role, you will be responsible for developing and implementing strategies that promote clinical excellence and operational efficiency. You will engage with cross-functional teams to optimize workflows and ensure that our services exceed industry standards.

Join our dynamic team at Olema, where we are dedicated to advancing innovative solutions in the field of clinical research. We are seeking a Senior Manager of Clinical Compliance & Inspection Readiness to lead our compliance initiatives and ensure readiness for regulatory inspections.In this pivotal role, you will be responsible for developing and implementing compliance strategies, conducting audits, and ensuring adherence to regulatory standards. You will collaborate with cross-functional teams to foster a culture of compliance and excellence within our clinical operations.

About Trial Library Founded in 2022, Trial Library, Inc. is a venture-backed startup focused on expanding access to clinical trials for cancer patients. The company’s AI-driven platform supports health equity in oncology by making precision medicine more accessible. Trial Library works closely with community oncology sites, patients, and industry partners to improve participation in clinical research and reshape cancer care. Role Overview: Chief Commercial Officer The Chief Commercial Officer (CCO) will lead Trial Library’s commercial strategy and play a central role in driving revenue growth. This executive position shapes the company’s commercial vision and oversees the development of a high-performing team. The CCO will build and strengthen partnerships across health systems, biopharma, and payers, influencing the company’s growth and market presence. Location San Francisco, CA

Overview:At Alleviate Health, we are pioneering the development of AI Agents designed to significantly expedite clinical trials through autonomous patient communication for recruitment and sustained support over the years, ultimately reducing billions in unnecessary expenditures. We are tackling the critical challenges faced by executives at major pharmaceutical companies worth over $100 billion.Having successfully bootstrapped, we are now proud to have secured a $4.3 million seed funding round led by a16z and are in search of exceptional talent to help address the most pressing issues in drug development, capitalizing on one of the most substantial opportunities within AI, while accelerating the delivery of transformative medicines to patients in need.Context:Conducting clinical trials is a complex and high-stakes endeavor, often fraught with challenges. Pharmaceutical companies invest tens of billions of dollars annually in research site management to qualify, screen, and maintain contact with hundreds of thousands of patients over extended periods. Approximately 80% of clinical trials face delays due to recruitment issues, with daily delays costing between $600,000 and $8 million.This overwhelming and labor-intensive effort of screening, recruiting, and retaining patients across myriad research sites is the primary bottleneck in clinical trials.About Alleviate:At Alleviate, we have developed state-of-the-art AI Agents that autonomously manage patient recruitment and retention in clinical trials. Our AI agents engage in over 100,000 conversations each month, achieving the following:Efficiently screening and directing patients to the appropriate trials.Collecting essential trial data from patients multiple times weekly.Providing accurate and timely responses to patient inquiries.

Join the Airwallex TeamAs a leader in global payments and financial solutions, Airwallex is revolutionizing the way businesses manage their financial operations. Our platform unifies payments, treasury, and embedded finance, empowering over 200,000 businesses worldwide, including industry giants like Brex, Rippling, and SHEIN.Founded in Melbourne, our dynamic team of over 2,000 innovators spans 26 offices globally. With a valuation of US$8 billion and support from premier investors, we are at the forefront of creating the global financial platform of the future. If you’re eager to make a significant impact and take on ambitious challenges, we invite you to be part of our journey.

Join Mercury as a Senior Associate in our Revenue Strategy team, where you will play a crucial role in shaping our growth and driving strategic initiatives. You will work closely with cross-functional teams to analyze revenue performance, develop actionable insights, and implement strategies that maximize profitability. Your analytical skills and strategic mindset will be essential as you navigate complex business challenges and contribute to our mission of empowering startups and entrepreneurs.