Clinical Trial Associate Salary at Caidya BETA

Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our company in a full-time, entry-level position that will rotate between our Chemistry, Manufacturing and Controls (CMC) and Research & Development (R&D) departments in the first year. This position is well suited for those looking for an entry-level position that is excited to learn all aspects of biotechnology drug development from early-stage research through drug product manufacturing. Candidates will be expected to accomplish defined work, as well as assist in approaching and solving complex scientific problems. Candidates should have demonstrated laboratory or manufacturing experience, with solid communication, technical aptitude, and problem-solving skills. Experience working in regulated, pharmaceutical/biotechnology R&D (GDP, GLP) and/or manufacturing environments (cGMP) is strongly preferred, but not required. Why Locus? Change the future of medicine and address a serious and unmet patient

Overview: RTI is a leader in multi-disciplinary research to address complex problems that impact human health. A historical strength, led by RTIs Technology Advancement & Commercialization (TAC) unit, has been aerosol exposure assessment and corresponding effects on human health through basic and applied research that spans the entire source-exposure-dose paradigm. Our research program focuses on health outcomes that leverage our advanced capabilities in aerosol exposure measurements and modeling, particle chemical speciation, data analytics, digital biomarkers of health impacts, and therapeutic drug delivery. We seek to grow our research program by adding expertise in respiratory health, specifically respiratory disease mechanisms, epidemiology, and environmental influences. This research will span the entire exposome from community to molecular levels by applying novel exposure assessment methods to improve public health both domestically and internationally. Responsibilities: To lea

Asklepios BioPharmaceutical, Inc. (AskBio) is a leading, clinical-stage gene therapy company founded in 2001 based on the work of adeno-associated virus (AAV) gene therapy visionary and pioneer, Jude Samulski, PhD. Since that time, our commitment to developing life-saving medicines that can potentially cure genetic diseases has never wavered. At AskBio, we've built a foundation of therapeutic programs, AAV manufacturing and a rich portfolio of patented technology. Our therapeutic focus includes neuromuscular, central nervous system, cardiovascular and metabolic diseases with clinical trials underway for Pompe disease, Parkinson's disease, and congestive heart failure. Our gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive AAV capsid and promoter library. We became a wholly-owned, independently operated, subsidiary of Bayer AG in late 2020 as a cornerstone of its newly formed Cell & Gene Therapy (CGT) platform. Our gl

Overview: Lead and perform Quality Assurance (QA) initiatives and duties at PharPoint Research, including all project and non-project activities performed. Responsible for assisting with the creation and implementation of quality initiatives at the company, including but not limited to: Standard Operating Procedures (SOPs) and training, computer systems validation (CSV), and Quality Management System (QMS). What you will do: Provide consultation and assist with decisions as it relates to the company and departmental QA strategy and departmental goals. Generate, approve and implement external and internal audit plans and processes. Organize and conduct internal audits in accordance with the internal audit schedule. Coordinate and host sponsor audits; manage and implement responses to audit observations. Plan, schedule, conduct and report investigator site audits, Trial Master File (TMF) audits and vendor audits. Coordinate and assist in regulatory inspections; assist with coordinating a

**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 . **Position:** Therapeutic Area Specialist (TAS) **Therapeutic A

Job Description Job Description We are looking for a Clinical Trials Project Manager II to join our team! APPLY DIRECTLY at https://cpcclinicalresearch.org/careers/ (internal title Clinical Operations Manager II) Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading! This role serves as the primary point of contact for industry sponsored clinical trials and Endpoint and Specialty Services activities. In this position you will: Oversee clinical operations management activities Define and monitor project scope, timelines and deliverables from project initiation to close-out. Identify project-specific training for team members and notify appropriate designee to ensure completion and filing of training documentation. Oversee trial-related activities. Track and approve vendor payments. Provide expert advice in the design, writing and/or review of all project

Position Summary: We are seeking an experienced and highly organized Clinical Trial Manager (CTM) to join our team and oversee the successful planning, execution, and delivery of clinical trials. The CPM will play a crucial role in the management of clinical development programs, ensuring that trials are conducted efficiently, on time, and in compliance with regulatory requirements. The ideal candidate will possess strong leadership, communication, and problem-solving skills, as well as a deep understanding of clinical trial management within a small biotech environment. Key Responsibilities: Project Leadership: Lead and manage the planning, execution, and close-out of clinical trials, ensuring timelines, budgets, and quality standards are met. Study Design & Strategy: Collaborate with internal stakeholders, including clinical operations, regulatory affairs, and medical affairs, to develop study protocols, budgets, and timelines. Vendor Management: Oversee relationships with external v

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Patient Engagement Associate to join our A-team (hybrid*/remote). As a Patient Engagement Associate at Allucent, you are responsible for supporting the Patient Engagement team, with the planning, development and execution of patient recruitment and engagement strategies appropriate to the awarded study needs.?? Additionally, the Patient Engagement Associate may support development of study specific branded patient and site facing materials. In this role your key tasks will include: + Support Patient Engagement team, in the preparation of presentation materials for Kick Off Meetings, Study Team Meetings, etc., as needed? + Provide support for Kick-Off Meetings and project meetings to support recruitment and retention discussions, as needed? + Assist in the de