Study Manager Salary at Lianbio BETA

Responsibilities: Provides SAS programming support to all clinical studies. Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables. Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD). Provides primary programming and QC support for any internally produced outputs. Reviews and approves SAS programming instructions and CDISC/ADaM specifications. Performs statistical analysis and simulations using SAS to support clinical trial design and data interpretation. Reviews and provides input on eCRF design, external vendor data specifications, edit checks, and other Data Management related documents to ensure appropriate data collection for statistical programming. Works closely with biostatisticians and data managers to identify data issues and generate queries that may impact statistical analysis and/or programming. Works closely with biostatisticians and other func

Project Coordinator Job no: 503750 Work type: Full-Time Location: University City - Philadelphia, PA Categories: Drexel University, College of Nursing and Health Professions Job Summary We are seeking a Project Coordinator who will play a crucial role in supporting the operations and initiatives of the CDMRP Dept of Defense Spinal Cord Injury Research Program funded research project "Improving Cardiometabolic Health in Individuals with Spinal Cord Injury Using Home-Based Interactive Virtual Gaming". Research Program Overview Physical/physiological changes following spinal cord injury (SCI) and barriers to physical activity place individuals with SCI at increased risk for chronic diseases exacerbated by physical inactivity and deconditioning. Physical activity, and exercise as a subset, can ameliorate these risks; however, individuals with SCI rank among the lowest on the physical activity and physical fitness spectrums. An urgent need therefore exists to address traditional barriers to

Ranked the overall #4 Best Civil Engineering Firm to Work for in the Nation (#1 in our size category) and residing on the list of the Engineering News Record (ENR)'s Top 500 Design Firms in the nation, TPD is currently hiring a Junior Environmental Scientist. TPD is seeking a mid-level enthusiastic, detail oriented, environmental scientist to join our team. Our ideal candidate has a strong work ethic, a desire to learn, the willingness to work cohesively within a team and the ability to work on multiple concurrent projects. Duties and Responsibilities include, but are not limited to: NEPA scoping and environmental document preparation. Preparation of Section 404/Chapter 105 water permits and supporting documentation. Preparation of Phase 1 Environmental Site Assessments. Conducting Phase 1 Bog Turtle Surveys and coordination of additional endangered species involvement. Wetland and Stream Identifications and Delineations. Preparation of Section 4(f)/2002 and Section 6(f) documentation

EOE Statement We are an equal employment opportunity employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status or any other characteristic protected by law.About the Organization Wills Eye Hospital, located in Philadelphia, Pennsylvania, is a global leader in the treatment of eye disease. Established in 1832 as the America's first eye hospital, we are one of the world's premier eye care facilities and the #2 best hospital in the nation for ophthalmology as ranked by U.S. News & World Report. Our clinical expertise, state-of-the-art diagnostic testing and advanced surgical capabilities make Wills Eye a worldwide referral center where more than 250,000 patients are treated annually. From common eye problems to rare sight-threatening diseases, Wills Eye provides general eye care and comprehensive ophthalmic specialty services that attract patients throughout the

Clinical Trial Associate – Leading Biotech in Cardiac & Gene Therapy A pioneering biotech company specializing in cardiac gene therapy is looking for a Clinical Trial Associate to join their team. This position offers the opportunity to work with breakthrough therapies focused on transforming cardiac care for patients with severe heart conditions. As part of this role, you’ll collaborate with leading experts and play an active role in the execution of high-impact clinical trials. Role Responsibilities A Clinical Trial Associate (CTA) plays a crucial role in the administration and coordination of clinical trials, which are research studies designed to evaluate the safety and efficacy of medical interventions such as drugs, devices, or treatment protocols. Below are the primary responsibilities and skills associated with the role: Key Responsibilities: Document Management: Maintain and organize essential trial documentation (e.g., study protocols, case report forms, informed consent form

Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across all disciplines. Today at Penn Medicine, someone will make a breakthrough. Someone will heal a heart, deliver hopeful news, and give comfort and reassurance. Our employees shape our future each day. Are you living your life's work? We are hiring for an Associate Director Oncology Research Operations to join our Cancer Services team at Penn Medicine Princeton Health. This role is a 5-year-grant-funded position that will extend into 2029, with the intention of seeking permanent and/or additional grant-funding past that date, as available.This individual must have oncology healthcare research expereince. Summary: The Associate Director Oncology Research Operations report

Clinical Trial Liaison Manager US-NJ-Princeton Job ID: 2024-1879 # of Openings: 1 Category: Clinical Trial Liaison BESTMSLs Overview The Clinical Trial Liaison Manager (CTLM) is a Hybrid office-based position with regular travel in the field. The role is based in North America, overseeing site trial delivery, subject recruitment, protocol adherence, and data quality. The CTLM represents the company in site relations, supports study teams with startup and recruitment, and manages in-field activities of the contracted CRO, focusing on the CRA team. The CTLM also addresses unresolved investigator concerns, engages with PIs for study updates and recruitment plans, and supports local site staff and trial team members. Additionally, the role provides project management support across the Medical and Clinical organization and ensures compliance with project plans, regulatory requirements, GCP, SOPs, and company policies. Responsibilities Essential Duties and Responsibilities Contributes to op

Overview Reporting to the Prison Teaching Initiative (PTI) Associate Director in the McGraw Center for Teaching and Learning, the PTI Assessment Specialist will conduct program evaluation of PTI's term-time and summer programming. A scholar of educational equity, trained in the historical, social, and ethical dimensions of the school-to-prison pipeline and in theories and methods of educational evaluation, the PTI Assessment Specialist will focus on equity in education practice by studying and evaluating PTI programs. The Assessment Specialist will regularly report findings to PTI's staff and other stakeholders. Once per academic year, the Assessment Specialist may lead a course for incarcerated undergraduates at one or more of the facilities PTI serves. Responsibilities Academic year program evaluationConduct program evaluation for term-time programming at one or more correctional facilities PTI serves, including assessment of course instruction, tutoring, co-curricular activities, st