will be an experienced investigator with strong regulatory or Fitness to Practise experience. You will have a detailed understanding.... Job Title: Regulatory Investigator Location: Hybrid (1-2 days per week in the London office) Day Rate...
: We are seeking a skilled and empathetic Housing Landlord Complaints Investigator to lead on Stage 2 complaint investigations..., regulatory body or similar. Experience of liaising with and responding to the requirements of a regulatory body. Ability...
Complaints Investigator – Housing association Pay Rate: £22.59 per hour Contract: Temporary Positions... Handling Code and other regulatory requirements. Maintain accurate records of all complaint-related activities within the CRM...
of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical.... Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports...
Writer (Regulatory) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built... and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures...
, and edit various scientific and regulatory documents, including clinical study reports, investigator brochures, CTD modules...We are a growing Scientific and Technology led regulatory consultancy. To support our growth, we are currently...
Updated: Yesterday Location: London, LND, United Kingdom Job ID: 25103769-OTHLOC-3526-2DR Description Sr Regulatory... study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed...
Medical Writer - Regulatory Submission Documents Syneos Health® is a leading fully integrated biopharmaceutical solutions... of documents, including clinical study protocols, amendments, reports, patient narratives, annual reports, investigator brochures...
and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP.... Assesses factors that might affect subject/patientâs safety and clinical data integrity at an investigator/physician site...
and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity.... Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments...
deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions... post activation through site closeout. This may include patient recruitment, investigator payments or other related...
- Denmark Hill London SE5 9RJ Job description Job responsibilities Act as sub-investigator and provide medical cover... safely, on time and to target, complying with the regulatory requirements. Engage as appropriate with all aspects of the...
About the Role You will work in close collaboration with the Chief Investigator at QMUL to coordinate the PINC-2... with Good Clinical Practice and relevant regulatory requirements. About You Candidates will hold an undergraduate degree...
Investigators and PIs at other centres. You will oversee the progress and performance of investigator sites, including efficient... in accordance with contractual agreements, trial protocol, trial-specific processes and systems, SOPs, regulatory and ethical...
((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site..., functional, investigator meetings). Follows up with team members on action items to closure. Maintains timely and effective...
is being responsible for managing complex projects across medical content development, Medical / Legal / Regulatory (MLR...-functional Medical Affairs projects, including medical content development, MLR (Medical/Legal/Regulatory) review processes...
management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good... at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site...
((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site..., functional, investigator meetings). Follows up with team members on action items to closure. Maintains timely and effective...
is being responsible for managing complex projects across medical content development, Medical / Legal / Regulatory (MLR...-functional Medical Affairs projects, including medical content development, MLR (Medical/Legal/Regulatory) review processes...