REGULATORY STUDY START UP jobs in United Kingdom

Job Summary Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory... a key role at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory advice to support...

-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...

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...

solely responsible for collection of the required documents for study start – up and during the trial. The role... assistance in preparing study documentation for trials, IRB/IEC submissions and documentation for regulatory dossiers. Being...

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...

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...

drawings created by Technicians Keep up-to-date with developments in regulatory legislation and guidelines that may affect... numerical analysis including the use of computer-based programmes to assist with the study of potable, surface and wastewater...

and consolidate final working drawings created by Technicians Keep up-to-date with developments in regulatory legislation.... Job Responsibilities will include: Undertake numerical analysis including the use of computer-based programmes to assist with the study...

deliverables. Participates in the set up and design during study start up (e.g., database set up) Lead medical monitoring team.... Collaborates with the Medical Writer on clinical/scientific and regulatory documents. Partners with Study Manager on study...

. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance... phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters...

policies, playbooks and procedure to ensure compliance with regulatory requirements, industry standards in an Operational role.... Office & WFH Policy: You'll have flexibility to work from home, meeting up with colleagues in the Epsom office three days...

Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting... RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams...

(as required to complete Foundation competences) by intended start date Is up to date and fit to practise safely and is aware of own training... research delivery alongside developing their own research study. We are privileged to have a dedicated Childrens Clinical...

: Pension; up to 26 days holidays (plus an additional two days at Christmas for office closure); training and development... opportunities; contribution to further studies and study leave allowance We reserve the right to close the role early...

interventional clinical study, as well as to progress AI-designed small molecules into the clinical setting. Our pipeline... and regulatory for small molecule, preferably in oncology Strong communication and stakeholder management skills Energy...

Submission. Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end... compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance...

Submission. Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end... compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance...