Clinical Trial Associate Salary at Janssen Global Services Llc BETA

Location: Boston, MA (Onsite) Focus: Oncology Job Overview: Join our client as the inaugural in-house Clinical Research Associate to oversee quality and patient safety, coordinating with a CRO and facilitating daily study operations. Primary Job Responsibilities: Partner with CROs for trial monitoring, maintaining compliance, data accuracy, and site relations. Perform site visits to ensure protocol compliance and manage essential documentation. Build relationships with study sites and vendors, and develop monitoring tools for data review. Assist in audit support, track enrollment, oversee data collection, and collaborate on study goals. Primary Job Requirements: Bachelor's degree with 6 years of clinical trials experience Skilled in managing complex oncology studies with a quality and compliance emphasis. Solid understanding of ICH/GCP, regulations, and relationship-building with sites/vendors. Willing to travel 50% and adept with Microsoft Office, EDC, CTMS, and eTMF. About Stratacuit

Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview Rhythm Pharmaceuticals, Inc. is seeking a Senior Trial Master File (TMF) Specialist to join as an integral member of the Clinical operations team, reporting to the Senior Director of Clinical Process and Quality-Control Management, (CPQM). This position will work closely

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leadin

Associate Director, Biostatistics We are looking for an experienced Associate Director, Biostatistics to lead statistical strategy, analysis, and oversight for clinical development programs. This role supports high-profile projects while managing a team of biostatisticians to ensure the highest quality and compliance with regulatory standards. Key Responsibilities: Strategic Leadership: Collaborate with cross-functional teams to develop statistical strategies for clinical trials (Phases I-IV). Provide input on protocol design, sample size calculations, and endpoint selection. Contribute to regulatory submissions and respond to agency queries. Team Management & Mentorship: Lead and mentor a team of biostatisticians, fostering growth and professional development. Assign resources, delegate tasks, and monitor project progress. Conduct performance reviews, provide constructive feedback, and develop training plans. Operational Oversight: Oversee the development of statistical analysis plans

Position Details Title Research Associate/Research Scientist (ACTG) School Harvard T.H. Chan School of Public Health Department/Area Center for Biostatistics in AIDS Research (CBAR) Position Description The Department of Biostatistics at the Harvard T.H. Chan School of Public Health has an immediate opening in the Center for Biostatistics in AIDS Research (CBAR) for a PhD-level Research Associate or Research Scientist statistician to work in ACTG: Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections. ACTG is a very large NIH-funded collaborative clinical trials network with an international research agenda focused on the treatment and cure of HIV infection and associated co-morbidities, particularly end organ diseases, tuberculosis, viral hepatitis, and emergent infections. The successful candidate will join over 100 statisticians, epidemiologists, and research staff collaborating on the design, monitoring, analysis, and reporting of Phase I through Phase IV clini

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . When you join BMS, you are joining a diverse, high-achieving te

Senior Clinical Trial Manager at Apellis Waltham, Massachusetts, United States Position Summary: The Senior Clinical Trial Manager is responsible for oversight and the overall management, planning, implementation, and execution of clinical trial(s) in a fast-paced environment with minimal oversight from the Associate Director/Director, Clinical Operations. The Senior Clinical Trial Manager actively contributes to and supports an environment of learning and process improvement. Key Responsibilities Include: Leads and/or oversees the trial team to execute and deliver the clinical trial in accordance with the clinical development plan/strategy, budget, and timeline. Authors and/or approves clinical trial documents and trial-related plans. Responsible for the clinical review and/or approval of CRFs, CRF completion guidelines, and the data review plan. Responsible for overseeing the identification and selection of investigator sites. Responsible for planning, conducting, and presenting duri

At Viridian Therapeutics, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets. Reporting to the VP of Clinical Development, the Clinical Development Scientist will support all aspects of clinical development (safety, science, and operations), including the safety and pharmacovigilance team and trial activities. Additionally, the Clinical Development Scientist will author and review key trial data-related documents and be responsible for the life cycle management of these documents. This role may be based in Waltham, MA, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion o