- Parexel (Boston, MA)
- …a sound business strategy. **Knowledge and Experience** : + Demonstrated understanding of clinical research , the drug development process, and industry ... Writer will research , create, and edit all documents associated with clinical research . Responsibilities also include: acting as primary client contact for… more
- Parexel (Boston, MA)
- …compliance and audit requirements in a GxP environment. + Demonstrated understanding of clinical research , the drug development process, and industry ... we are dedicated to improving patient lives through innovative clinical research and regulatory solutions. As a...ICH-GCP. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study … more
- Parexel (Boston, MA)
- …a sound business strategy. **Knowledge and Experience** : + Demonstrated understanding of clinical research , the drug development process, and applicable ... Medical Writer will research , create, and edit all documents associated with clinical research . The Senior Medical Writer may operate as the project lead… more
- Parexel (Boston, MA)
- …+ Basic understanding of the drug development process. + Good understanding of Clinical Study Management including monitoring, study drug handling ... SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility...drug supplies and drug accountability at study site. Prepares study drug … more
- Parexel (Boston, MA)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:...Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction,… more
- Parexel (Boston, MA)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... the set-up, running and close-out of sites in a clinical trial. **Monitoring Responsibilities and Study Conduct:**...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
- Parexel (Boston, MA)
- …off adverse events report for accuracy and clinical importance, relationship to the study drug as well as for severity and seriousness; provide sponsors with ... epidemiology background research + Provide safety content review of clinical protocols, study reports, Investigators Brochures, and other related documents… more
- Parexel (Boston, MA)
- …looking to leverage their clinical expertise in the dynamic field of clinical drug development. As a medical expert and strategic partner, you'll play ... to complex medical and protocol-related questions from sites and study teams **Shape Drug Development Strategy** +...Parexel?** At Parexel, you'll join a global leader in clinical research with a mission to improve… more
- Parexel (Boston, MA)
- …practice + Interact with clients and regulatory authorities + Review publications and clinical study reports + Travel to, attend, and actively contribute to ... describe advanced statistical techniques and interpret results + Familiarity with regulatory/ research guidelines on drug development, GCP, and statistical… more
- Merck (Boston, MA)
- …MD or MD/Ph.D. with a minimum of 10 years' experience in oncology biomarker studies and translational clinical research **Required Experience and Skills:** + ... Biomarker Development, Biomarker Research , Clinical Development, Clinical Research , Diagnostics Development, Drug Development, Immuno-Oncology,… more
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