Job Title : Local Study Manager / Associate Director - Remote Job Location : Uxbridge, UK Job Location...
, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role... in an office-based model; and Fluency in English & local language Medpace Overview : Medpace is a full-service clinical...
-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the... in English & local language Medpace Overview Medpace is a full-service clinical contract research organization (CRO...
, Instagram, YouTube and LinkedIn. Job Description Purpose The Sr. Specialist, Country Study Start Up proactively drives... and change management in the adoption of new technologies and processes. Note: Sr. Specialists will report into their local...
Sr. Local Trial Manager – Sponsor Dedicated. Local Trial Management services provide local management of a clinical... Clinical Practice (GCP), local regulatory requirements. Prepares or contributes to high level budget estimate in response...
Arterial Hypertension (PAH) and Rare Diseases. The Local Trial Manager II (LTM II) is responsible for local management... to participate in trial.Collaborates with the Global Product Lead (GPL), CTM/GTL, local management/Country Head and other study team...
Manager II (LTM II) is responsible for local management of a clinical trial (or Medical Affairs data generation activity....Collaborate with the Global Product Lead (GPL), CTM/GTL, local management/Country Head, and other study team members to select the...
Job Description - System Coordinator and Reporting Manager (MER0003I7Q) System Coordinator and Reporting Manager.... Communicate with central and local support for Logistics and barcode/WH operation systems and follow up with any necessary...
. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. Please submit... representative or SrCRA dealing with medical institutions and physicians or as a site manager working on site. Knowledge and skills...
laws, rules, and regulationsServe as primary Sponsor contact for operational project-specific issues and study... and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when...
, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery... in clinical environment as a medical representative or SrCRA dealing with medical institutions and physicians or as a site manager...
Investigator Contract Manager, you will be responsible for the development of complex investigator grant estimates, contracting... Plan. Coupled with being able to provide specialist legal, operational, and financial contracting support to the study...
, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery... in clinical environment as a medical representative or SrCRA dealing with medical institutions and physicians or as a site manager...
Buenos Aires, reporting to Senior Manager.Oversee day to day activities from BA team, composed of Seniors and Staffs... work schedule: (2 office days).Competitive salaries and revisions.Club La Nación Premium.20 annual study days.Subscription...
laws, rules, and regulations - Serve as primary Sponsor contact for operational project-specific issues and study... - Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when...
and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager, the role... or CRA operational issues to meet commitments in a timely manner in coordination with the study CRM.Attend local Investigator...
and close-out activities. The Senior Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant.... As the Senior Site Manager, you will:Act as primary local company contact for assigned sites for specific trials, may...
role:The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the... clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities...
and addressing risks. Communication with client, project team members and local regulatory specialists on study sites status...Reg & Start Up Manager – Sponsor Dedicated Direct and manage the delivery of all required site activation...
and all other applicable laws, rules, and regulations Serve as primary Sponsor contact for operational project-specific issues and study... Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when...