years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
thinking, alignment-building and discretion to tailor documents to study needs. Independently lead data cleaning activities...Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out...
years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
Available to travel on short notice The role will lead and provide direction to the Clinical Project Team to ensure all trial outputs... (from protocol development to Clinical Study Report) are delivered on time, within budget, and with high quality, in adherence...
years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical... programs Performs hands-on clinical data management tasks to support clinical studies, including, but not limited to reviewing...
! Responsibilities: Essential Duties and Responsibilities: Provides clinical supervision and clinical documentation review... for assigned Beyond the Classroom school-based staff. Supports the development of standardized clinical best practices...
years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
years in lead role for clinical development programs with medical devices leading toward FDA filing / approvals Thorough..., and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
to data management teams and stakeholders Act as Data Management Study Lead for multiple clinical trials Manage vendor...Responsibilities: Lead clinical data management activities for pivotal trials, ensuring data quality and integrity...
. Position Specifics This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up..., and monitoring visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease...
. Responsible for scientific oversight, data integrity and quality of the clinical trial(s). Represent the study team... in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
The Senior Lead Data Manager (“LDM”) serves as the primary point of contact for data management and is responsible... activities; including oversight of assigned study team member activities and external vendors Serve as the study project manager...
Sr. Manager / Associate Director, Regulatory Affairs US Lead Direct Hire Full-Time Role Salary Range... study reports, clinical protocols/study reports, Investigator Brochures, CMC information/data) and contribute to content...
Sr. Manager / Associate Director, Regulatory Affairs US Lead Direct Hire Full-Time Role Salary Range... study reports, clinical protocols/study reports, Investigator Brochures, CMC information/data) and contribute to content...