Study Coordinator Salary at Casimir BETA

Position: Research Study Coordinator, Infectious Diseases Location: Boston, MA Schedule: 40 hours per week ABOUT BMC: At Boston Medical Center (BMC), our diverse staff works together for one goal - to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience. You'll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you'll have the tools you need to take charge of your own practice environment. JOB RESPONSIBILITIES Protocol and Study Document Development Coordinates development of study protocols, informed consent forms (ICFs), and standard operating procedures (SOPs) Develops data collection tools (quantitative and qualitative) and leads design and validation of electronic data capture (EDC) systems

Associate Scientist: Preformulation - Contract - Cambridge MA Proclinical is seeking an Associate Scientist to join our client's team in Cambridge, MA. Primary Responsibilities: The successful candidate will be instrumental in supporting the transition of novel small molecule compounds from Discovery into Development. Your work will focus on pre-clinical and clinical programs, utilizing your expertise in analytical techniques and early drug development processes. Skills & Requirements: Bachelor's degree in chemistry, analytical chemistry, pharmaceutics, chemical engineering, or material sciences. Experience with the Discovery and Development interface is desirable. Familiarity with common excipients and volumetric glassware. Proficiency with UPLC/HPLC and Empower Software. Interest in small molecule and pre-clinical formulation development. The Associate Scientist: Preformulation responsibilities' will be: Prepare buffers and common lab solutions. Conduct analytical experiments using X

Director, Global Clinical Dev. Programs- Permanent - Cambridge, MA Proclinical is seeking a dynamic leader to spearhead the development of new therapy areas to join the team. Primary Responsibilities: The successful candidate will provide strategic leadership and execution of clinical development operations, offering unique career development opportunities on a global scale. You will work closely with the VP of Clinical Development in Neuroscience, managing study operations and ensuring effective cross-functional collaboration. Skills & Requirements: Extensive experience in Aesthetics Clinical Operations, particularly in managing Ph1-3 global aesthetic medicine studies. Proven track record in hands-on study management and executing projects efficiently. In-depth knowledge of FDA, EMA, and other national regulations, ICH guidelines, GCP, and key Clinical Operations principles and tools. The Director, Global Clinical Dev. Programs' responsibilities will be: Design and implement strategie

***Candidate must be local in order to be in the office 1 day per week! Reporting to the Director, Clinical Operations, the Senior Clinical Trial Manager is responsible for leading the execution of clinical studies on schedule and on budget. The Senior Clinical Trial Manager ensures studies are conducted efficiently and with quality, adhering to timelines and budget, and in alignment with the company’s strategic goals. The level reflects the experience, skill level, and capacity to manage larger and/or more complex studies, projects or programs. Responsibilities (including, but not limited to): Accountable for project related efforts for the delivery of studies or programs that are critical to a product’s clinical development, ensuring that they are completed on time, within budget and in compliance with SOPs, regulations and ICH/GCP guidelines. Supports external vendor selection and management process and assists in the development of RFP’s and vendor oversight plans. Provide clinical

Who We Are: Founded in 1891 by a group of visionary volunteers, The Trustees of Reservations (The Trustees) is the nation's premier conservation and preservation organization. The Trustees' preserves, for public use and enjoyment, properties of exceptional scenic, historic, and ecological value in Massachusetts. Our properties are open to all, and we thrive by involving as many people as possible in all that we do. We aim to protect special places for future generations to enjoy in perpetuity, and have helped protect more than 50,000 acres, including 27,000+ acres on more than 120 reservations that are open to the public. As a non-profit conservation organization, we are funded and supported entirely by our visitors, supporters, volunteers, and our 100,000 Member households. We encourage you to learn more about The Trustees on our website, www.thetrustees.org. Posting Information: Salary/Hourly Rate: $17 - $19/hour Hours per week: 35-40/week, Mondays-Fridays, 8:15AM-3:30PM Job Classifi

As one of the nation's top schools of social work, Boston University School of Social Work (BUSSW) is dedicated to the pursuit of excellence in education, research, and evidence-based practice to advance social justice and to solve the most pressing societal problems of the 21st century. The BUSSW and Center for Innovation in Social Work (CISWH) currently invites applications for a Project Manager (PM) to coordinate and manage a five-year NIH funded study conducted at the CISWH and Boston Medical Center. Study goals are to train community health workers to deliver behavioral counseling in a primary care setting to reduce substance use and to improve mental health in Spanish and in English. The Project Manager is responsible for coordinating and overseeing the day to day study operations of this hybrid study which combines a randomized effectiveness trial with a study of implementation feasibility, across different sites. There is travel required within the state. Tasks will include: ov

Responsibilities: CLINICAL TRIAL OPERATIONS Clinical Research Managers (CRM) are responsible for the oversight of their disease group's clinical trial portfolio and all related regulatory, compliance and performance metrics requirements. The CRM will oversee the processing of protocols through the Institutional Review Board (and other institutions' IRBs) when appropriate. The CRM will collaborate with the Clinical Trials Office (CTO), the Office for Human Research Studies (OHRS) and the Quality Assurance for Clinical Trials (QACT) to fulfill local and federal requirements governing human clinical trials. The CRM will Identify and manage operational, logistical, and regulatory challenges related to the conduct of clinical trials and acts as a leader in overseeing their resolution. The CRM will assist the principal investigator in developing the protocol budget, in collaboration with the Research Administration and the Grants and Contracts offices. Work with grant managers and other fina

Planet Pharma's client is looking for an Associate Director / Senior Medical Writer, who will be responsible for providing medical writing support for the development of complex clinical documents for regulatory submissions including, but not limited to clinical protocols, informed consents (ICFs), clinical study reports (CSRs), investigator brochures (IBs), patient narratives, annual reports and other key clinical and regulatory documents. This individual will support the overall strategy for all medical writing processes according standards. Key Accountabilities/Responsibilities: Manage medical writers (in-house FTEs and contractors, and external vendors) who are individually contributing to the MW activities for a variety of regulatory documents Author clinical content and project manage SME contribution of regulatory documents to develop content for regulatory submissions that is well-organized, consistent, accurate, and that complies with applicable company SOPs, style guide, lexi