- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Description Exciting opportunity at MSK: Join our team as aResearch Project Associate ! We're looking for a dynamic clinical research professional to support ... determined by management. Key Qualifications: + 2-4 years of Clinical Research / Project Management experience. + 1-2 years of regulatory experience, 2+ years… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and… more
- Takeda Pharmaceuticals (Columbus, OH)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing...regulatory writing expertise and mentorship to NRWS and Research and Development (R&D) staff members. + Involves in… more
- AT Still University (Mesa, AZ)
- **Description** The Research Project Coordinator II is responsible for the successful planning and implementation for multiple ATSUs clinical and academic ... they are delivered on time and following the respective research protocols. The Research Project ...consultation to principal investigator(s) and other key stakeholders (eg, research team members, funders, regulatory bodies) on… more
- Bausch + Lomb (Bridgewater, NJ)
- … regulatory compliance. * Communicate with stakeholders to manage project priorities, deadlines, and budgets to meet organizational and department objectives. ... communication with internal and/or external partners to ensure satisfaction with project results. **Requirements** Qualifications: * Minimum Associate degree,… more
- ManpowerGroup (Stanford, CA)
- …Transplant studies. * Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets ... Our client is looking for Clinical Research Coordinator Associate located at Stanford,...protosscols** . **DUTIES:** * Serve as primary contact with research participants, sponsors, and regulatory agencies for… more
- Colorado State University (Fort Collins, CO)
- …training in support of the University's land grant mission. The Research Associate II will work with project manager(s), senior staff, and student staff ... external community and business partners as required with each project and grant. The Research Associate...to research . + Knowledge of human subjects research regulatory practices. + Excellent verbal, editing,… more
- Astrix Technology (Fremont, CA)
- Regulatory Affairs Associate Regulatory Affairs Fremont, CA, US Pay Rate Low: 34.00 | Pay Rate High: 36.00 + Added - 07/10/2024 Apply for Job **_Our client ... is a global, research -driven pharmaceutical focusing on treatment options for diseases and...option to date. The company is looking for a Regulatory Affairs Associate to join the team.… more
- ICON Clinical Research (Brentwood, TN)
- …Central CDP Review Team (CDPRT) and Sponsor. **What you need for Study Start Up Associate I - Regulatory Submissions** * A high school diploma or local ... Study Start Up Associate II - US, Brentwood, TN ICON plc...activities. * Experience of Clinical Trial operations and meeting regulatory guidelines * Proficient project management skills.… more
- Abbott (Alameda, CA)
- …for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Associate Director Regulatory Affairs - US New Product Introduction ... a vision for the organizational unit assigned. + Create project plans and timelines. + Lead functional groups in...industry (eg, medical products). + 5-7 years' experience in regulatory preferred but may consider quality assurance, research… more
- ICU Medical (Southington, CT)
- …these changes for ease of regulatory agency review. . Represents Global Regulatory Affairs at research and development meetings and presents agreed upon ... regulatory positions. May serve as a lead regulatory representative to an assigned product or project team. * * *Knowledge & Skills* . Review and approve… more
- Stanford University (Stanford, CA)
- …and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets ... Cancer Clinical Research Coordinator Associate - Blood &...**Core duties include*:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate… more
- Stanford University (Stanford, CA)
- …Coordinate collection, processing and analysis of study specimens and data. + Manage research project databases, develop flow sheets and other study related ... Clinical Research Coordinator Associate **School of Medicine,...**Duties include:** + Serve as the primary contact for research participants, sponsors, and regulatory agencies. Coordinate… more
- GE Aerospace (Niskayuna, NY)
- …construction projects - from initial scoping to owner turnover **Job Description** **Facilities Project Manager:** GE Aerospace Research will continue to play a ... that support research at the GE Aerospace Research site. As a Project Manager -...scope, estimate and oversee the construction of projects. OR Associate degree in a technical, construction or engineering field… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director, Associate General Counsel, Global Regulatory Compliance Date: Oct 17, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: ... new people to make a difference with. **The opportunity** The Sr. Director, Associate General Counsel, Global Regulatory Compliance role reports directly to the… more
- University of Michigan (Ann Arbor, MI)
- …program. May be responsible for coordination of operation with another department in a research project . Coordinates the processing and analysis of data and the ... Research Lab Specialist Inter (Underfill to Associate...cGMP regulations (USP823 and 21 CFR212). + Contribution to regulatory documents required for clinical PET tracer filings such… more
- Novo Nordisk (Plainsboro, NJ)
- …reports, preclinical reports, investigator brochures, application summary documents, etc. + Research and analyze the evolving competitive and regulatory ... in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
- Stanford University (Stanford, CA)
- …and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets ... Clinical Research Coordinator Associate (On-Site) **School of...include** **_*_** **:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate… more
- Stanford University (Stanford, CA)
- …and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets ... Clinical Research Coordinator Associate **School of Medicine,...for the overall implementation of an assigned set of research protocols assuring efficiency and regulatory compliance.… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …growth, thereby accomplishing corporate goals. **Responsibilities** + Develop and implement US regulatory strategy for assigned project (s). + Strategize and plan ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Summary** This role… more