Senior Clinical Manager

Overview: The Senior Safety Specialist is responsible for ensuring accurate collection, database entry, review, and reporting of clinical trial and post-marketing safety data. They will be required to assist senior staff in signal generation, safety analysis activities, and to be proactive in the development and implementation of departmental processes and...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

**Clinical Research Associate - World Leading CRO - Permanent** We are seeking an experienced Clinical Research Associate to take on an exciting opportunity with an international CRO that is continuing to lead from the front in the industry. Utilising their unique experience and global reach, this CRO has regularly demonstrated why they are market leaders...

The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and IIa) in different therapeutic areas.   As...

Are you a passionate and experienced professional in the field of surgery? Are you looking for an exciting opportunity to contribute to the growth of a leading manufacturer of Surgical Robots in Germany? We are seeking a dynamic Clinical Sales Representative to join our client's team and make a significant impact on the healthcare industry.As a Clinical...

Proclinical are partnering with a pharmaceutical organisation who are recruiting for an individual to join their team. This role is on a permanent basis with the ability to work remotely from anywhere in Germany. The position that is currently available in this organisation, is for an Associate Direct Clinical Data Management, Oncology.Please ensure that you...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas. We currently offer the exciting...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

Proclinical is seeking a dedicated and experienced professional for the role of Head of Corporate Clinical Research & Development. This role involves overseeing the departments of Clinical Operations, Clinical Strategy & Development, and Clinical Systems. The successful candidate will be responsible for the medical-scientific strategy of developing new...

Proclinical is seeking a dedicated and experienced professional for the role of Head of Corporate Clinical Research & Development. This role involves overseeing the departments of Clinical Operations, Clinical Strategy & Development, and Clinical Systems. The successful candidate will be responsible for the medical-scientific strategy of developing new...

Proclinical is seeking a dedicated and experienced professional for the role of Head of Corporate Clinical Research & Development. This role involves overseeing the departments of Clinical Operations, Clinical Strategy & Development, and Clinical Systems. The successful candidate will be responsible for the medical-scientific strategy of developing new...

Our client is a forward-thinking medical devices company specializing in transfusion.Responsibilities:- Train medical staff (including anesthetist nurses and doctors, perfusionists, biomedical engineers) on-site in the comprehensive use of the medical device, covering all aspects from installation to usage, including tips and tricks.- Provide assistance...

Trilogy Writing & Consulting is currently looking to hire Senior and Principal Medical Writers (m/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our...

Hobson Prior are seeking for a Clinical Research Coordinator to join a fantastic CRO on a contract basis located in Frankfurt. Our client is focused on maximising the speed and effectiveness of the people who conduct clinical trials. Please note that to be considered for this role you must have the right to work in this location. **Key...

As a Senior Medical Writer (m/w/d), you will: - Prepare a variety of clinical regulatory documents as the lead writer in collaboration with members of client authoring teams and supported by other writers, as appropriate. - Ensure that all documents are produced according to agreed timelines, monitor and manage project budgets, adhere to relevant SOPs, and...

Trilogy Writing & Consulting is currently looking to hire Senior and Principal Medical Writers (m/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our...

Trilogy Writing & Consulting is currently looking to hire Senior and Principal Medical Writers (m/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our...

... Your role: As Senior Manager Regulatory CMC, you will lead and drive global regulatory CMC activities for New Chemical Entities (NCE) and/or drug-linkers for Antibody Drug Conjugates (ADC) during all clinical phases (I, II, III) and first .. -...