Reporting to the VP, Clinical Operations, CARGO is seeking a. Clinical Trial Associate. to play a crucial part in the Study Management Team. The successful candidate will coordinate various administrative aspects of the sponsor’s project management and oversight activities. The individual will partner closely with the Clinical Project Managers and Clinical Research Associates to provide administrative expertise to multiple clinical study manageme...
Our Client, a major medical devices company (a subsidiary of a major pharmaceutical and healthcare products company) is seeking several experienced research professionals for its medical devices group. The position is responsible for providing project management coordination and the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies. You Must reside in the Boston, MA. Phil...
Equillium (. www.equilliumbio.com. ). is a clinical stage biotech company focused on developing novel therapies for severe and life threatening autoimmune and inflammatory diseases. Its lead program, EQ001, is a first-in-class anti-CD6 mAb that targets a novel co-stimulatory pathway involved in the activation, proliferation, differentiation and trafficking of T effector cells in autoimmune and inflammatory diseases. Equillium is currently conduct...
Company DescriptionAt Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective All in all, our expertise l...
The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational strategy and and execution of clinical studies, supporting the strategy as defined in the Clinical Development Plan. Provide support for essential daily clinical study activities, including regulatory inspection readiness, following established protocols under the general management of the CTA Manager. Work with Clinical Operations Manager, study ...
Company Description. Bicycle Therapeutics (NASDAQ: BCYC) is a clinical-stage biopharmaceutical company developing a novel class of medicines. Our pipeline includes Bicycle Toxin Conjugates® as well as fully synthetic Bicycle® systemic immune cell agonists and Bicycle tumor-targeted immune cell agonists (Bicycle TICAs) focused on oncology indications with high unmet medical need. Bicycle is headquartered in Cambridge, UK, and our US operations run...
Company Overview. Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the care of people living with rare melanocortin-4 receptor (MC4R) pathway diseases. Working at Rhythm means that you are part of a team that’s passionate about transforming the lives of people living with hyperphagia (pathological, insatiable hunger) and severe obesity caused by rare MC4R pathway diseases. We recognize the courage it takes ...
Description. Assist in trial CDAs and agreements preparation with legal and other functions along with the concerned authorities at the clinical trial sites. Prepare templates for budget estimates and facilitates communication between internal and external partners during contract and budget phases of the CT project. Manage the clinical sites referencing, purchase orders, invoicing processes, regular accruals. Prepare the documentation package fo...
Wave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Our RNA medicines platform, PRISM, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and prevalent disorders. Our toolkit of RNA-targeting modalities includes editing, splicing, RNA interference and antisense silencing, provi...
Report. This position reports to the Director, Clinical Research and Evidence Generation. . Job Summary. . The Clinical Trial Associate (CTA) plays a key role in supporting Glooko’s Clinical Research projects. This role will be a good fit for candidates who desire to learn and grow professionally while gaining experience in clinical trial management. The CTA will assist with existing clinical projects and management of accounts/clinical studies, ...
Responsibilities. . Assist the team in ensuring that quality clinical trials are conducted per protocol, in a timely fashion, and in compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and established study budgets. . Create, maintain, and track information for keys study activities and needs. . Establish and maintain access to various systems for the conduct of the clinical trials such as lab, imaging, IxRS, eTMF, etc. . Collabora...
