Senior Clinical Trial Manager

Become a Pioneer in the Sleep Fitness RevolutionJoin Eight Sleep, where our mission is to enhance human potential through exceptional sleep quality. As the world's first sleep fitness company, we are transforming the concept of well-being and creating cutting-edge hardware, software, and AI technology to facilitate optimal sleep. Our innovative products are …

The Alliance for Clinical Trials in Oncology Foundation is dedicated to advancing cancer clinical research by expanding the capabilities of the Alliance for Clinical Trials in Oncology. Our mission is to address significant treatment challenges through large-scale clinical trials aimed at discovering innovative methods for the prevention, treatment, and cure of various cancers, including leukemia, lymphoma, and solid tumors such as breast, prostate, lung, and gastrointestinal cancers. We also strive to educate the medical community on effective cancer diagnosis, treatment, and prevention strategies.In 2014, we established the Alliance Foundation Trials, LLC (AFT), a wholly-owned subsidiary focused on conducting impactful cancer clinical research in collaboration with industry partners.We are currently seeking a Clinical Research Associate (CRA) to play a crucial role in the management and execution of clinical trial operations across AFT studies. The CRA will be responsible for site management and study start-up activities, including conducting feasibility assessments, supporting site selection, maintaining trial master files (eTMF), and overseeing clinical trial management systems (CTMS). The ideal candidate will work closely with CROs, vendors, and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards throughout the study lifecycle. Join our team of dedicated professionals passionate about transforming cancer care.

At Veeva Systems, our mission is to accelerate the delivery of therapies to patients through innovative cloud solutions tailored for the life sciences industry. As a trailblazer in the SaaS sector, we achieved over $3 billion in revenue last fiscal year and are poised for significant future growth. Our core values—Doing the Right Thing, Customer Success, Employee Success, and Speed—guide every aspect of our operations. In 2021, we distinguished ourselves by becoming a public benefit corporation, legally committed to balancing the interests of all stakeholders including customers, employees, society, and investors. As a Work Anywhere organization, we empower our employees to work in their preferred environments, whether from home or in the office, fostering their success and well-being. Join us as we transform the life sciences industry and create a positive impact for our customers, employees, and communities.

About PrileniaPrilenia is an innovative biopharmaceutical company dedicated to delivering groundbreaking therapies for individuals impacted by severe neurodegenerative diseases. Our global team is passionate and committed to advancing medical science, particularly through our development of pridopidine, an oral investigational neuroprotective treatment targeting ALS and Huntington’s disease (HD). Collaborating with Ferrer, we are poised to initiate critical late-stage trials that may lead to global approval for ALS and HD by the first half of 2026. Role OverviewWe are on the lookout for a motivated Regional Clinical Trial Manager to join our expanding team. This pivotal role involves overseeing and managing the operational activities of global pivotal trials in neurodegeneration. The successful candidate will possess extensive clinical research experience, particularly in clinical project management, and will have a proven track record of successfully managing global pivotal clinical trials for biotech sponsors. Experience with rare diseases, particularly ALS or HD, is highly desirable. This position requires a self-starter who can work independently across multiple projects while effectively collaborating within a matrix global team environment. The Regional Clinical Trial Manager will report directly to the SVP, Head of Clinical Operations.

Veeva Systems is a mission-driven organization and a leader in industry cloud solutions, dedicated to accelerating the delivery of therapies to patients. As one of the fastest-growing SaaS companies globally, we achieved over $3 billion in revenue last fiscal year and continue to explore extensive growth opportunities. Our core values include: Doing the Right Thing, Ensuring Customer Success, Fostering Employee Success, and Maintaining Speed. We are not just another public company – in 2021, we made history by becoming a public benefit corporation (PBC), legally committed to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we promote flexibility, allowing you to work from home or in the office, enabling you to excel in your preferred environment. Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.

Veeva Systems is a purpose-driven leader in the industry cloud sector, dedicated to assisting life sciences companies in accelerating the delivery of therapies to patients. As one of the most rapidly expanding SaaS organizations in history, we achieved over $3 billion in revenue in our last fiscal year, with significant growth opportunities on the horizon. Our core values at Veeva include: Doing the Right Thing, Customer Success, Employee Success, and Speed. We are not just an ordinary public company; we made history in 2021 by becoming a public benefit corporation (PBC), committed to balancing the interests of customers, employees, society, and investors. As a Work Anywhere organization, we foster flexibility, allowing you to work from home or in the office to thrive in your ideal environment. Join us in transforming the life sciences industry as we strive to make a positive impact on our customers, employees, and communities.

Axiom Talent Platform is hiring a Clinical Trial Counsel to focus on commercial and R&D legal matters within the pharmaceutical and life sciences sector. This role is based in Boston, supporting teams involved in clinical trials and drug development. What you will do Advise on legal issues that arise during clinical trials and throughout the drug development process. Work closely with commercial and research teams to address regulatory compliance questions. Help ensure company practices follow current laws and industry standards. Requirements Background in providing legal counsel for clinical trial activities. Understanding of regulatory requirements in the pharma and life sciences industries. Skill in balancing compliance with the needs of research and innovation.

Veeva Systems is not just a leader in the industry cloud; we are a mission-driven organization dedicated to accelerating the delivery of therapies to patients. As one of the fastest-growing SaaS companies in history, we achieved over $2 billion in revenue last fiscal year and are poised for continued growth.At Veeva, our core values—Do the Right Thing, Customer Success, Employee Success, and Speed—guide our actions. We made history in 2021 by becoming a public benefit corporation (PBC), committed to balancing the interests of all stakeholders, including customers, employees, society, and investors.As a Work Anywhere company, we champion flexible work arrangements, allowing you to thrive in an environment that suits you best, be it at home or in the office.Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.

Join our dynamic team at Alimentiv as a Senior Clinical Operations Lead, where you will play a pivotal role in shaping the future of clinical trials. We are looking for a strategic thinker with extensive experience in clinical operations to lead our initiatives and ensure the successful execution of clinical studies.

Join AbbVie as a Senior Clinical Research Associate in Boston, where you will play a pivotal role in advancing our clinical research initiatives. You will be responsible for overseeing clinical trials, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to drive project success.

Company Overview Avalyn Pharma is innovating the landscape of pulmonary fibrosis treatment through a groundbreaking pipeline of inhaled formulations. These approved medications are expertly designed to minimize systemic exposure and deliver targeted therapy directly to the affected areas. Pulmonary fibrosis, characterized by lung tissue scarring, diminishes lung function and quality of life, contributing to increased mortality rates. Conventional therapeutic options may slow disease progression but often come with significant toxicities that limit their application. Avalyn’s inhaled approach directly addresses the underlying causes of pulmonary fibrosis, aiming to enhance patient outcomes with reduced systemic side effects. Currently, Avalyn’s AP01, an optimized inhaled formulation of pirfenidone, is under investigation in the MIST Phase 2b study for progressive pulmonary fibrosis (PPF). This formulation has demonstrated clinical proof-of-concept with better efficacy and safety profiles compared to existing treatments, having been evaluated in over 150 patients with various forms of pulmonary fibrosis. Furthermore, Avalyn has completed two Phase 1 studies for AP02, an inhaled formulation of nintedanib for idiopathic pulmonary fibrosis (IPF), with plans for a Phase 2 clinical trial in the works. For more details, please visit avalynpharma.com and follow us on LinkedIn.

Welcome to knownwell, a pioneer in weight-inclusive healthcare solutions. Join our innovative team that is transforming obesity care delivery through a comprehensive approach that includes weight management, primary care, nutrition counseling, and health coaching. Our unique care model integrates both in-clinic and virtual services to ensure that patients receive the support they need, exactly when they need it.With $50 million in funding—including a $25 million round led by CVS Health Ventures and supported by a16z Bio + Health, Flare Capital, MassMutual, and Intermountain Ventures—we are rapidly expanding access to evidence-based obesity care across the nation. As the Clinical Research Coordinator (CRC), you will oversee and synchronize all facets of our clinical trials. Your role is vital in ensuring compliance with regulatory requirements, sponsor expectations, and Good Clinical Practice (GCP) guidelines. You will serve as the primary point of contact between the clinical research team, patients, and external stakeholders, facilitating the efficient and timely execution of clinical research initiatives.

Join our dynamic team as a Clinical Investigator specializing in Breast Oncology or Hematology. In this role, you will conduct groundbreaking research and clinical trials, contributing to the advancement of cancer treatment. You will collaborate with top researchers and healthcare professionals to drive innovative solutions in patient care.

Join Olema Pharmaceuticals as a Senior Manager, Clinical Compliance & Inspection Readiness, where you will play a pivotal role in ensuring our clinical operations meet the highest standards of compliance and readiness for inspections. You will lead initiatives that drive adherence to regulatory requirements and best practices, helping us bring innovative therapies to patients efficiently and safely.

Veeva Systems is a pioneering organization dedicated to transforming the life sciences sector through innovative industry cloud solutions. Our mission is to expedite the delivery of therapies to patients, and our impressive growth trajectory reflects our commitment, having surpassed $3 billion in revenue in the last fiscal year. At Veeva, our core values are paramount: Do the Right Thing, Customer Success, Employee Success, and Speed. In 2021, we made history by becoming a public benefit corporation (PBC), ensuring a balanced approach to serving the interests of our customers, employees, society, and investors. As a Work Anywhere company, we empower you to choose your ideal work environment, whether at home or in the office, to maximize your potential. Join us in revolutionizing the life sciences landscape, with a commitment to making a meaningful impact on our customers, employees, and the communities we serve.

Veeva Systems Inc. is a forward-thinking organization and a leader in cloud solutions for the life sciences sector, dedicated to accelerating the process of bringing new therapies to patients. As one of the fastest-growing SaaS companies globally, we achieved over $2 billion in revenue last fiscal year and are poised for further growth.At Veeva, our core values drive us: We prioritize doing the right thing, achieving customer success, fostering employee success, and ensuring speed in our operations. In 2021, we made history by becoming a public benefit corporation (PBC), which legally commits us to balance the interests of our customers, employees, society, and investors.As a Work Anywhere company, we empower you to choose your work environment, whether from home or the office, to help you thrive in your preferred setting.Join us on our mission to transform the life sciences industry and make a meaningful impact on our customers, employees, and the communities we serve.

At Morgan & Morgan, the impact of our work is profound. We stand as the last bastion for millions of Americans against the might of insurance companies and corporate entities. Our dedicated team, spanning attorneys in all 50 states, client support staff, and creative marketing professionals, plays a pivotal role in championing consumer rights. With over 6,000 employees, we are united by a singular mission: For the People.Full Job DescriptionWe are seeking a passionate and skilled Trial Attorney to join our esteemed General Liability Litigation team. This position involves managing a diverse and complex caseload, encompassing all stages from pre-litigation to trial. You will represent plaintiffs in a variety of cases, including but not limited to slip and fall incidents, security negligence, wrongful death, and dog bite claims.Why Morgan & Morgan?1. Since our establishment in 1988, we have successfully recovered over $25 billion for the people, with an impressive $8 billion recouped in the last two years across all 50 states, Washington, DC, and the US Virgin Islands.2. Our commitment to growth has seen our national marketing campaigns expand from $250 million to over $500 million since 2023, solidifying our position as the nation's leader in out-of-home marketing spend. Recently, we welcomed Geico Insurance’s former Head of Auto Marketing as our new Chief Marketing Officer.3. Unlike many of our competitors, Morgan & Morgan is proud to employ attorneys who truly engage in trial work. Last year, we tried 320 cases, and we aim to double that in the coming years. Our attorneys gain invaluable courtroom experience and are expected to participate actively in trials.4. Our team has access to state-of-the-art case docket management software and extensive litigation resources, ensuring that you have the tools necessary for optimal case development.

Join our dynamic team at Precede as a Senior Clinical Laboratory Associate, where your expertise will play a pivotal role in advancing our clinical testing capabilities. You will lead laboratory operations, ensuring the highest standards of quality and accuracy in all testing procedures.Your responsibilities will include overseeing clinical trials, managing laboratory staff, and collaborating with cross-functional teams to interpret complex data. We are looking for a detail-oriented professional who thrives in a fast-paced environment and is passionate about contributing to innovative health solutions.

Join our dynamic Medical Research & Development team at Alimentiv, where your expertise in biostatistics will play a crucial role in advancing clinical trials and data management. As a Senior Statistician, you will be responsible for utilizing biostatistical methodologies to guide the statistical planning, design, analysis, and reporting throughout the project life cycle, adhering to both organizational and regulatory standards.Your role as a subject matter expert will involve providing statistical support to project teams, quality/study auditors, and external stakeholders. Contribute to the promotion of Alimentiv as a leading global research organization by engaging in the development, publication, and reporting of project data. Additionally, you will have the opportunity to lead and mentor a team of statisticians and SAS programmers, fostering their professional growth and enhancing team capabilities.Positions available: 1 (Remote-based, Canada or USA)

Join Whoop as a Clinical Product Manager, where you will play a pivotal role in shaping the future of health technology. In this dynamic position, you will collaborate with cross-functional teams to develop innovative clinical solutions that enhance user experiences and outcomes. Your expertise will be essential in driving product development from conception to launch, ensuring that our offerings align with clinical standards and user needs.