- Aequor (Raleigh, NC)
- …- Negotiate clinical site contracts (ie Disclosure Agreements, Clinical Trial Agreements, Service Agreements) using appropriate guidelines and collect necessary ... signatures for contract execution; Participate in site/legal/finance meetings as required to resolve contract issues; Negotiate site budgets from base budget and payment milestones using appropriate guidelines; Escalate contract and budget issues as… more
- Insmed Incorporated (NJ)
- …the future of science, we're in. Are you?About the Role:The Associate Director, Programming provides technical leadership and ensures adequate programming support ... packages Significant knowledge of the drug development process, clinical trial methodology, and relevant regulatory requirements for drug approval Significant… more
- Merck & Co. (North Wales, PA)
- …and vaccines for the benefit of patients and global human health.The Senior Associate will provide administrative support to senior leaders in the Biostatistics and ... field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering… more
- Merck & Co. (Upper Gwynedd, PA)
- …to manage clinical development projectsAssist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in ensuring ... Clinical Immunology, Clinical Investigations, Clinical Medicine, Clinical Research, Clinical Trial Planning, Clinical Trials, Clinical Trial Support,… more
- Merck & Co. (Rahway, NJ)
- …manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed ... Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical Trials Monitoring, General Cardiology, Medical Monitoring,… more
- Aequor (Thousand Oaks, CA)
- …Quality experience Or Bachelor's degree and 8 years of R&D or Quality experience Or Associate degree and 10 years of R&D or Quality experience Or High school diploma ... of pharmaceutical/biotech industry o Document and process management experience o Change management expertise o Clinical Trial experience and/or knowledge of ICH GCP more
- Insmed Incorporated (NJ)
- …with serious diseases. In this role, you'll be reporting to the Associate Director, Biostatistics.The Insmed Summer Internship Program is designed to give you ... on innovative statistical methodology and application related to clinical trial design and analysis.Complete assigned goals and objectives that support… more
- Cordis (Irvine, CA)
- …that address unmet and critical medical needs. **Responsibilities** We are seeking a Clinical Trial Associate in Irvine, CA to join our clinical study team in ... space to help execute a randomized, multi-center IDE clinical trial . You will perform various duties and responsibilities as...from start-up phase through study completion + Maintain internal Trial Master Files (TMFs) and prepare study TMF for… more
- University of Miami (Coral Gables, FL)
- …(https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . CORE JOB SUMMARY The Clinical Trial Disclosure Associate within the Research ... activities and requirements for clinical trials disclosure. The CTD Associate reports to the Sr. Clinical Trial ...CTD Associate reports to the Sr. Clinical Trial Disclosure Associate . The objective is to… more
- Lilly (Indianapolis, IN)
- …the trial sponsor in recent years. The role of the Clinical Trial Label Regulatory Compliance Associate is to participate in maintenance and interpretation ... of the clinical trial (CT) material label requirements and CT material regulations,...product. To accomplish this, it is necessary for the Associate to develop collegial and mutually productive relationships across… more
