STUDY START UP REGULATORY jobs in UNITED KINGDOM, United Kingdom

study start-up - desirable; Hands-on experience preparing, reviewing, and submitting regulatory documentation is beneficial...-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the...

study start-up is essential; Hands-on experience preparing, reviewing, and submitting regulatory documentation; Knowledge...-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the...

-based Contract Specialist, Study Start-Up to join our Clinical Operations team. This position plays a key role in the study... start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing the...

Study Start Up Associate / Regulatory Submissions At ICON, it’s our people that set us apart. Our diverse teams... sector, and you’ll be helping shape an industry. Study Start Up Associate / Regulatory Submissions As a member of the...

, you will have the opportunity to advance study start-up and regulatory activities by understanding client objectives. You will be in... ability in the leadership of a team of individuals in study start-up Knowledge of applicable international regulatory...

development of study-specific documentation. Review site-level informed consents and other patient-facing study start-up... materials. Oversee the setting up and maintenance of study systems. Contribute to investigator meeting preparation...

documentation. Review site-level informed consents and other patient-facing study start-up materials. Oversee the setting up...Salary: £380 - £400 per hour Job type: Contract * Discipline: Project/Study Manager (CSM/CPM) * Location: United...

required essential documents for study start-up and throughout the conduct of a trial. You will conduct on-site training and motivate the...The Recruitment Co are recruiting for a Study Monitor (Clinical Operations) to join our clients expanding team. A world...

responsible for ensuring collection of the required essential documents for study start-up and throughout the conduct of a trial... preparing study documentation for trials, IRB/IEC submissions and documentation for regulatory dossiers. You will be solely...

, Global Study Start-up Managers, Pharmacovigilance, Business Development, Auditors and/or Inspectors for Regulatory... Global Start-up Manager/PM ensuring submissions are performed according to internal and client expectations. Plan realistic...

, Global Study Start-up Managers, Pharmacovigilance, Business Development, Auditors and/or Inspectors for Regulatory... Global Start-up Manager/PM ensuring submissions are performed according to internal and client expectations. Plan realistic...

by Technicians Keep up-to-date with developments in regulatory legislation and guidelines that may affect design work Working... including the use of computer-based programmes to assist with the study of potable, surface and wastewater systems Undertake...

study of potable, surface and wastewater systems Keep up-to-date with developments in regulatory legislation and guidelines...

, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase... visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team...

study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start-up... with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations...

to: Contracts support; review protocols in support of new requests for proposal Study management activities and study start-up... of activities to support the start-up, management, and completion of patient services for clinical research studies...

Coordinate the activities associated with site start-up and overall trial management Coordinate study level investigational... Study Budgets and timelines Coordinate study level investigational product arrangements and study start-up and management...