Position: Manufacturing Associate, Cell Therapy in Devens, MA Devens - MA - US R1596698 Posted a day ago ## Manufacturing Associate, Cell Therapy in Devens, MADevens - MA - USFind out how well you match with this job • * Working with Us • * Challenging. Meaningful. Life-changing. Those aren’t words that are usually ...

Bristol-Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Devens, MA. This role involves 24x7 quality collaboration and oversight in manufacturing, ensuring adherence to company policies and global cGMP standards. Applicants should have at least 4 years of cGMP experience and st...

Position: Senior Specialist, Quality Assurance Shop Floor, Cell Therapy Devens - MA - US R1601155 Posted [...] ## Senior Specialist, Quality Assurance Shop Floor, Cell Therapy Devens - MA - USFind out how well you match with this job • * Working with Us • * Challenging. Meaningful. Life-changing. Those aren’t words ...

A leading biotechnology company in Cambridge, Massachusetts is seeking an MSAT Associate Director. This role involves leading a team responsible for the pancreatic cell maturation and aggregation process, collaborating with partners, and guiding team members. Candidates must hold a BSc in relevant fields with 8 year...

A biotechnology company in New Jersey is seeking a Senior Engineering Associate/Associate Engineer in Manufacturing Science and Technology. This role involves developing and implementing manufacturing processes for cell therapy programs, including the management of tech transfers and execution of process improvement...

Bristol-Myers Squibb is hiring a Specialist, Lead Clinical Manufacturing Associate in Devens, MA. The role demands expertise in cGMP bioprocessing and cell therapy manufacturing, supporting operations to deliver transformative treatments. Join a passionate team that prioritizes quality and safety in cell therapy ini...

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company r...

Position: Cell Therapy Manufacturing Associate — Night Shift (Onsite) Bristol-Myers Squibb in Summit, NJ, is hiring a Manufacturing Associate for the Cell Therapy team. This role involves manufacturing human blood-derived components in a cGMP cleanroom, adhering to strict regulatory standards. The position offers ...

About Made Scientific Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combines the agility ...

Bristol Myers Squibb in Summit, NJ is hiring a Manufacturing Associate for Liso-cel CAR-T Manufacturing Operations. This role involves operating equipment for blood component production, adhering to safety standards and quality regulations while working the night shift from Wednesday to Saturday. Ideal candidates wi...

The Associate Director, External Operations, Cell Therapy – External Supply Management, leads external manufacturing partner operations. These operations span a network of CDMOs and external partners supporting cell therapy across autologous, allogeneic, in vivo, and new platforms. You will create operational govern...

Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. It’s an exciting time to be part of Team Olema, with our transformation into a fully integrated oncology company well underway, top-lin...

Overview The Director of Drug Safety & Pharmacovigilance provides strategic and hands-on leadership for pharmacovigilance activities supporting a clinical-stage biotech pipeline in inflammatory and oncology diseases. This role is responsible for establishing and executing global safety strategy across early- and mid...

GlaxoSmithKline is looking for a Senior Scientific Director in Clinical Safety for Oncology to lead safety strategy and governance while ensuring robust benefit-risk assessments. This role demands significant expertise in pharmacovigilance and drug safety within the pharmaceutical sector. The ideal candidate will h...

Scienta is seeking a Director, Regulatory Affairs CMC to join their growing Regulatory team. This position plays a key role in advancing their oncology pipeline by leading Regulatory CMC strategy for biologic programs. The ideal candidate will have extensive Regulatory Affairs CMC experience, knowledge of FDA regul...

Position: Senior Regulatory Affairs – Oncology | Equity + Flexible PTO About us: Our purpose at Dispatch is to help create a world where all cancer patients can be cured. We’re humbled by the opportunity to work together as a team on some of the most pressing medical challenges of our time. To achieve our purpose...

Global Regulatory Affairs Manager Develop and execute global and regional regulatory strategies for oncology assets, ensuring optimal labeling and approvals while maintaining compliance with internal and external requirements. Collaborate with cross‑functional teams to shape development plans and regulatory interact...

Position: Senior Biostatistician & Programmer for Oncology Trials Legend Biotech Corporation in Somerset, New Jersey is looking for a Sr. Manager, Biostatistician/Programmer to support clinical development programs. The role involves transforming clinical trial data into analyses that inform decision-making and req...

A leading biotechnology company is looking for a Biostatistical Programming Senior Manager to oversee statistical programming for Oncology products. This position involves leading a team, ensuring quality in statistical deliverables, and effectively managing regulatory submissions globally. Ideal candidates should p...

Who Are You? As a Principal Statistician, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to lead and support clinical trials for drug development, with the opportunity to leverage your experience in late-phase trials and regulatory submissions for Oncology studies. ...

Who Are You? As a Principal Statistician, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to lead and support clinical trials for drug development, with the opportunity to leverage your experience in late-phase trials and regulatory submissions for Oncology studies. ...

LAB Labcorp Early Development Laboratories Inc. is searching for a Senior Lead Biostatistician in North Carolina to support oncology research initiatives. The role includes overseeing statistical design and execution for multiple studies, ensuring quality outputs and collaboration with various teams. The ideal cand...

LAB Labcorp Early Development Laboratories Inc. is searching for a Senior Lead Biostatistician in North Carolina to support oncology research initiatives. The role includes overseeing statistical design and execution for multiple studies, ensuring quality outputs and collaboration with various teams. The ideal cand...

Position: Oncology Biostatistician: Real-World & Genomic Analyses Apr is looking for a Biostatistician to join their oncology research team, supporting data quality and analysis in a collaborative environment. The ideal candidate will have advanced statistical expertise and the ability to contribute to impactful re...

A leading contract research organization is seeking a Clinical Data Manager to oversee oncology trials. The role includes leading data management activities, developing data management plans, and collaborating with various teams to ensure project success. Candidates should have at least 7 years of experience in clin...

A leading educational institution in Washington, D.C. is seeking a Research Data Coordinator 1 to manage data for oncology clinical trials. Responsibilities include capturing and organizing data, collaborating with study teams, and ensuring compliance with confidentiality regulations. The role requires a High School...

Welcome! We're excited you're considering an opportunity with us! To apply to this position and be considered, click the Apply button located above this message and complete the application in full. Below, you'll find other important information about this position. The West Virginia University Health System, the s...

The University of North Carolina at Chapel Hill is seeking a Soc/Clin Research Specialist to advance cancer research through managing clinical trials. This role requires a Bachelor’s degree and experience in oncology clinical trials, with a focus on recruitment and regulatory compliance. The ideal candidate demonst...

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize...

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwi...

Position: Oncology Clinical Development Scientists (Senior Manager) Position Summary You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Oncology portfolio. Key Responsibilities • Clinical development exper...

Pfizer seeks an experienced professional for clinical oversight within the Late-Stage Oncology portfolio. You will ensure data integrity and quality for clinical trials, author essential documents, and lead teams in the collection and analysis of data. The ideal candidate holds a PhD/Pharm D or equivalent and has e...

Job Title: Hematology/Oncology Physician Location: Saginaw, MI Organization: Covenant HealthCare Opportunity Overview: Covenant HealthCare is seeking a Board Certified/Board Eligible Hematology/Oncology physician to join our nationally recognized Cancer Care Center. This is an exceptional opportunity to join a leadi...

Job Description Physician Assistant – Oncology Clinical Trials (Phase I / First-in-Human) Outpatient Cancer Center | Bronx, NY | 4 days/week (10-hour shifts) | Low daily patient volume | Union role + strong benefits If you’re a PA with 1+ year of oncology experience and you’re craving a role where you can be deta...

JOIN OUR TEAM! The Physician will manage patients with ongoing hematological/oncological medical conditions, in collaboration with other services/sections of the Fredericksburg Health Care Center (FxHCC) The provider is accountable to the FxHCC Medicine Section Chief, assuring the most effective delivery of care. ...

The CRC (Clinical Research Coordinators) work within the Breast Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for t...

Syneos Health/ in Ventiv Health Commercial LLC is looking for a Clinical Scientist specializing in Oncology to collaborate with the Medical Director and engage with external experts. The role involves developing medical plans, overseeing medical reviews, and ensuring data integrity. This position offers comprehensi...

The Research Data Specialists will support the Breast Oncology clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; and the monitor...

Worldwide Clinical Trials, located in North Carolina, seeks a Clinical Scientist to lead clinical data review and ensure data integrity. The role involves partnering with various study teams to analyze clinical data and communicate insights effectively. Ideal candidates will have an advanced clinical degree and ove...

Location: Laurel Syneos Health/ in Ventiv Health Commercial LLC in Maryland is seeking a Clinical Scientist in Oncology to collaborate closely with the Medical Director. The role includes developing medical plans, conducting data reviews, and ensuring project milestones are met. The successful candidate will engag...