REGULATORY SUBMISSIONS STUDY START jobs in United Kingdom

Provide regulatory submissions strategic advice and guidance to the Regulatory Submissions Manager (RSM), Medpace project team... submissions Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges...

phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters... for submissions and all necessary authorizations. Identify regulatory complexity and challenges and offer creative and practical...

, 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...

compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance... BA/BS degree, science / technology field preferred Demonstrated relevant regulatory submissions experience Expert...

compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance... BA/BS degree, science / technology field, preferred Demonstrated relevant regulatory submissions experience Expert...

for trials, IRB/IEC submissions and documentation for regulatory dossiers. Solely responsible for ensuring collection of the... required essential documents for study start-up and throughout the conduct of a trial. You will conduct on-site training and motivate the...

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

Description Senior Site Start-Up & Regulatory Specialist Syneos Health® is a leading fully integrated biopharmaceutical solutions... improvement of quality in all Site Start-Up (SSU) components at the country level where assigned (submissions, essential document...

, engaging in operational and regulatory reporting, resolving customer inquiries, and contributing to operational change... review all in-scope submissions and processes these in line with agreed service levels. Execute tasks related to the...

agencies (FDA, EMA) to support clinical trial regulatory submissions Liaise with other functions to enable quality clinical... and selection, and provide assistance with study start-up activities Participate in Investigator meeting planning and execution...

organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory... development from the start, with the insight they will have in market needs (e.g., product demand, target selection, sample...

maintaining standard operating procedures, supporting training as qualified, engaging in operational and regulatory reporting... Lifecycle Support: Thoroughly review all in-scope submissions and processes these in line with agreed service levels. Execute...

Type: Full-time, permanent Start Date: We are currently recruiting for start dates throughout 2024, which occur on a monthly.... To date, the HTA team at Costello Medical have worked on over 200 submissions to national reimbursement agencies, including the...

for external training, interest-free travel loan scheme, discounted gym membership, and Role Type: Full-time, permanent Start... Date: We are currently recruiting for start dates throughout 2024, which occur on a monthly basis Location: this role is available in...

FOR Function as a Clinical Data Manager (CDM) to coordinate the day-to-day support of CDM deliverables from study start-up through... required in a scientific field. BENEFICIAL Experience with regulatory submissions WE ARE BAT At BAT we are committed...

. Clinicology offers a full range of services including site start-up, monitoring, project management, regulatory submissions... assigned projects through study start up, recruitment and close out. Develop study materials, study plans and timelines...

and study start-up Maintain activities spreadsheet for studies Regular communication with global study stakeholders... of activities to support the start-up, management, and completion of patient services for clinical research studies...