Clinical Research Principal & Associate Salary at Vesper Medical Inc BETA

About Us: At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees by providing competitive rates and compensation, a comprehensive employee benefits programs, attractive working conditions, and the chance to build and explore a career opportunity by offering professional development. Discover why Cooper University Health Care is the employer of choice in South Jersey. Short Description: Assists the research manager, principal Investigator, and other members of the research team with preparation of IRB protocols, consent forms, data entry, and other tasks as needed. Completes and maintains all study documents as required. Assists with the identification and recruitment of study participants. Work as a team player w

University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023. Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelp

Job Description Job Description Job Title: Director- Clinical Development, Ophthalmology Reports to (Title): CEO Location: Remote Exempt/Non-Exempt: Exempt Direct Reports: No Department: Clinical Science Job Summary: Responsible for driving the US or global clinical development strategies and execution for assigned investigational and/or marketed products in the Ophthalmology Therapeutic Area (TA). The incumbent will be responsible for providing critical input into the strategy, development, management and implementation of Phase 1-4 clinical studies by closely working with the Clinical Ops team; providing medical input on the clinical development plan. Essential Job Functions: Clinical Development Expertise & Strategy The Medical Director, Ophthalmology, will provide overall clinical scientific leadership for Exegenesis Bio’s Ophthalmology programs and have responsibility for our clinical development strategy and execution of clinical trials in this area Develop the study protocol syn

About the Role We are seeking a dedicated Clinical Research Coordinator to join our team. This role is essential to our ongoing liquid biopsy research study for GI cancer, working directly with study patients, pharmaceutical companies, and research assistants. Candidates must have site-side, patient-facing clinical research experience, including handling data and documentation in a setting where participants come on-site for studies. Key Responsibilities Organize and manage files, projects, and research data. Collect, process, and verify research data, samples, and specimens following strict protocols. Accurately enter data into databases and documents. Perform routine quality control checks to ensure data integrity and compliance with study protocols. Coordinate patient visits, ensuring referring physicians are notified. Handle and process blood, urine, and stool specimens at patient visits. Maintain case report forms per FDA guidelines, ensuring accuracy against medical records. Proc

Job Description Job Description Duties: Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Act as subject matter expert (SME) on one or more assays and train new laboratory personnel. Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs, and change control Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus. Hands on experience in bioburden, endotoxins, mycoplasma, gram

Job Description Job Description Duties: Perform daily GMP quality control laboratory testing activities Perform data analysis and final result reporting to support product lot release with adherence to turnaround times Perform all activities with respect to GMP compliance Support thorough GMP investigations for out of specification test results Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role Hands-on laboratory experience with cell counting, cell viability, flow cytometry, ELISA/potency assays, endotoxin, and/or sterility techniques. Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance – PPO, HMO & HSA Dental & Vision insurance 401k plan

Job Title: Clinical Project Manager Reports to: Director, Clinical Operations We are seeking a highly organized and experienced Clinical Project Manager (CPM) to oversee and lead clinical research projects from initiation through completion. The ideal candidate will possess a deep understanding of the clinical trial process, strong leadership and financial management skills, and the ability to manage multiple stakeholders, budgets, timelines, and regulatory requirements. The CPM will work closely with a cross-functional team and will partner with internal and external team members/key stakeholders, ensuring alignment of activities with study projects and timelines to ensure the successful execution of studies in compliance with GCP, regulatory guidelines, and company standards. Responsibilities Project Planning and Execution Identify key milestones and deliverables, ensuring alignment with study goals and timelines Lead planning, initiation, execution, and closure of clinical studies,

Study Start Up Specialist Must Haves: Must have previous experience with Clinical Research and experience with study start up, feasibility, and budget & contract experience Hours: 40 hours per week, Monday-Friday 9am-5pm. 3-4 days onsite Contract Duration: contract-to-hire Benefits: Medical, Dental, Vision, time off, paid holidays off, etc. Job Overview: The company seeks a highly motivated and detail-oriented Clinical Research Study Start-Up Specialist to join our dynamic team. The ideal candidate will be responsible for managing and overseeing the start-up phase of clinical trials, ensuring that all required regulatory, site, and logistical components are completed in a timely and efficient manner. This role requires strong organizational skills, a deep understanding of clinical trial processes, and the ability to collaborate with cross-functional teams to ensure smooth and successful study initiation. Works with minimal supervision. This role will be the main contact for all trial s