- Sanofi Group (Cambridge, MA)
- … subteam to design clinical studies and to create an abbreviated and full clinical study protocol. + Oversee the execution of clinical studies in ... **Job Title:** Clinical Research Director **Location** : Morristown,...+ Contribute to data review, interpretation and publication of clinical study results. + Represent Clinical… more
- Sanofi Group (Cambridge, MA)
- …the Clinical Science Operation (CSO) team to implement selected clinical trial (s) within the GCDP, including study initiation, study conduct and ... **Job Title:** Clinical Research Director - RBD **Location:**...accountable for the appropriate design, execution, and analyses of clinical trials within the GCDP. + The… more
- Sanofi Group (Cambridge, MA)
- …plan through internal management review + Lead a clinical sub team to design clinical studies and to create study protocols + Execute the clinical ... trial , scientific and digital methodologies + Pro-actively progress study execution + Oversee the execution of clinical... study execution + Oversee the execution of clinical studies in compliance with internal SOPs,… more
- Sanofi Group (Cambridge, MA)
- **Job title** : Clinical Research Director, I and I,...studies and to create an abbreviated and full clinical study protocol + Oversee the execution ... be critical in helping our teams accelerate progress. The Clinical Research Director (CRD), Immunology & Inflammation...CDP through internal management review + Leads a clinical subteam to design clinical … more
- Actalent (Burlington, MA)
- …clinics and hospitals to educate medical professionals and patients about the clinical trial , distributing study materials, posting recruitment materials, ... Job Title: Part-Time Clinical Research Coordinator Job Description We...researchers and community physicians to facilitate patient recruitment for clinical trials Essential Skills + 2+ years… more
- IQVIA (Boston, MA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...* Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good… more
- Beth Israel Lahey Health (Boston, MA)
- …including preparation of consent forms to the IRB on all clinical trials (industry, cooperative groups and PI initiated studies ), and respond to IRB ... lives.** The Sr. Regulatory Specialist supports regulatory compliance for clinical research at Beth Israel Deaconess Medical...comments on applications submitted and work with study team in getting studies activated for… more
- ICON Clinical Research (Cambridge, MA)
- …at ICON, you will play a crucial role in designing, conducting, and analyzing complex clinical research studies . You will leverage your expertise to drive ... site ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...collaborate across departments to ensure the successful execution of clinical trials that advance new treatments and… more
- ICON Clinical Research (MA)
- …functional areas. + Ensures site non-IMP study supplies are adequate for trial conduct. + Ensures that clinical drug supplies are appropriately used, ... will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence....complete and accurate at any time point during all trial phases. Responsible in close collaboration with study… more
- Dana-Farber Cancer Institute (Weymouth, MA)
- …outside organizations in the completion of + clinical research trials . Clinical : + Coordinates study enrollment, protocol treatment, and completion ... cancer patients and their families undergoing therapy in a clinical research trial . Strong interpersonal,...of study requirements for patients participating in clinical trials . + Works collaboratively and functions… more