Clinical Trial Manager - Marlton, NJ

CenExel Clinical Research is seeking a Clinical Trial Manager to oversee the management of clinical research studies and personnel assigned to those studies. · ...

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. · ...

The Clinical Trial Manager is responsible for the management of clinical research studies and personnel under the direction of the Clinical Director. · ...

We are seeking a Trial Supply Manager to join our diverse and dynamic team. · ...

This individual is responsible for the planning and inventory management of clinical supplies during the execution phase of a clinical trial according to timelines and will be responsible to stay within budget, and meet all SOP, GMP and regulatory requirements. · ...

We're seeking an experienced Clinical Trial Manager for our Early Oncology team. You will manage day-to-day operations of assigned trials and lead cross-functional trial teams. The ideal candidate has strong knowledge of ICH/GCP guidelines and regulatory requirements. · The succe ...

The Clinical Trial Manager / Senior Clinical Trial Manager will oversee the clinical portion of the budget to ensure efficient resource allocation. · ...

As Local Trial Manager - Oncology (Hematology) you will be responsible for ensuring top-quality end-to-end trial delivery at a country level. · ...

We are currently seeking a Trial Supply Manager to join our diverse and dynamic team. · We are looking for someone who can manage the planning procurement and distribution of clinical trial supplies to study sites. · You will contribute to the success of our clinical programs by ...

We're proud to foster an inclusive environment driving innovation and excellence, · and we welcome you to join us on our mission to shape · the future of clinical development. · ...

The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical operational activities at the trial and site level. · • Participates in clinical research activities including management of clinical study sites · • Develops clinical trial timelines ...

The Local Trial Manager - Oncology (Hematology) will ensure top-quality end-to-end trial delivery at a country level. · They will manage local vendors including set up of vendor purchase orders and execution of local milestones. · The L-LTM will oversee resourcing country-level r ...

Job summary: · This position is responsible for the supply planning and inventory management of clinical supplies required to support global clinical research and development studies during phases 1-4. · Responsibilities:Collaborating with internal and external Customers and Serv ...

Ensure top-quality end-to-end trial delivery at a country level managing consistency of Local Trial Management duties and processes. · ...

We are currently seeking a Trial Supply Manager to join our diverse and dynamic team. · ...

The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, · vendor oversight & delivery, compound training, and other activities. The TDM is responsible for country and regional oversig ...

The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical operational activities at the trial and site level. · ...

+The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities. · + · +Create and update critical trial-specific documen ...

Local Trial Manager to ensure top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties and processes. · Central IRB and other local vendors including set up of vendor purchase orders, invoice review and approval, and chan ...

+The Lead Trial Delivery Manager is responsible for executing study-level activities for clinical trials in oncology. · +Create and update critical trial-specific documents. · Manage vendor set up and management of day-to-day study vendor activities. · +Qualifications/Requirement ...