Clinical Trial Regulatory Lead

The Position Clinical Trial Regulatory Lead  The Pharma Development Regulatory (PDR) organization develops and maintains the licensees that permit Roche to market and sell its life improving therapies worldwide. We are the stewards of the safety and efficacy of medicines, collaborating with regulators of every country in which Roche does business...

6000! That’s the number of associates in the Novartis Institutes for BioMedical Research - (NIBR). This division is the innovation engine of Novartis, focusing on powerful new - technologies that have the potential to help produce therapeutic breakthroughs for patients! - Based on our understanding of cancer at the molecular, cellular and organismal...

An experienced Clinical Trial Leader is required to join a global pharmaceutical company onsite in Basel. **What you will be doing**: - Responsible for leading and matrix managing the multidisciplinary team and support functions as assigned - Author of the clinical study protocol and other study essential documents. Responsible for ordering and management...

Proclinical are recruiting for a Clinical Trial Associate, on behalf of a mid-sized MedTech organisation based in Basel, Switzerland. This is a full-time, 12-month contract role with option to go permanent, offering hybrid / remote working. **Overview**: Our partner develop truly innovative drug-eluting devices for the treatment of complex cardiovascular...

Hobson Prior are looking for a Clinical Trial Leader to join a fantastic pharmaceutical organisation on a contract basis located in Basel. Our client is focused on improving and extending the lives of many. Please note that to be considered for this role you must have the right to work in this location. **Key Responsibilities**: - For this role, you will...

To strengthen our team in Switzerland, we are looking for a Clinical Trial Associate who will support our customers’ clinical trial. In this role, you will support our clients on the coordination, data sampling and documentation management.Your DutiesTracking and reporting trial documentsUpdating clinical trial databasesPrepare, collate, distribute and...

**The Life Science Career Network** Our client is a biotechnology company, developing next generation cancer vaccines based on viral vector technologies. We are currently looking for a **Clinical Trial Supply Manager** for a contract role, fully remote, for applicants living in Switzerland. Your responsibilities include conducting and overseeing all supply...

Social network you want to login/join with:Clinical Trial Manager - Sponsor Dedicated, BaselClient:IQVIALocation:BaselJob Category:OtherJob Reference:e68eafbf69a2Job Views:9Posted:21.01.2025Expiry Date:07.03.2025Job Description:Clinical Trial Management and Central Trial Oversight services provide for the regional/global coordination of clinical trial...

General Description: - Role will support the study team with Clinical Operations tasks, and/or support compilation and quality of the trial master file (TMF) - Demonstrates basic clinical operations knowledge and strong organizational skills - Implements best practices and shares lessons learned with team and other colleagues, as appropriate - Adheres to...

General Description: - Role will support the study team with Clinical Operations tasks, and/or support compilation and quality of the trial master file (TMF) - Demonstrates basic clinical operations knowledge and strong organizational skills - Implements best practices and shares lessons learned with team and other colleagues, as appropriate - Adheres to...

Senior Clinical Trial Scientist 100% 12-month contract based in Basel area. The Senior Clinical Trial Scientist is representing clinical science as core member of the Clinical Trial Team and contributes to the following trial-level activities: Main Responsibilities: Collaborates closely with the Clinical Trial Physician (CTP) on relevant trial-related...

Proclinical have partnered with a mid-sized Biotech who are recruiting for a Clinical Trial Leader. They have had several successful product launches over last few years and are presently running multiple phase III trials within highly multifaceted therapy areas. You will be responsible leading a several phase III studies in highly complex therapy areas...

**The Role**: Leads and continues to build the Clinical Trial Application (CTA) regulatory group, responsible for providing effective operational and regulatory support for assigned regulatory clinical trial submissions and maintenance activities, including preparation and submission of regulatory dossiers, and maintenance of regulatory databases and...

A Mid-sized Pharma are recruiting for an experienced Clinical Trial Associate to join their growing on a 6 month contract with option to become a permanent employee after the initial assignment. This is a great opportunity to join a busy clinical team working across a variety of highly complex trials whilst taking on a wide range of responsibilities. The...

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global...

Looking for a talented professional to join one of the largest global pharmaceutical companies as a Clinical Development Medical Director, to be part of a diverse team at the forefront of innovation. What the role involves: - Oversight of the clinical development of assigned programs and driving execution of the clinical development plan - Provide clinical...

Job DescriptionWe are seeking an experienced Medical Director who will lead and/or support early-stage clinical projects from entry into a human through proof of mechanism and proof of concept. You will leverage your expertise to translate innovative molecules into potentially transformative therapies for patients with severe brain disorders. By marrying...

**T he Role**: Do you want to join a team that wants to redefine technology for content creation and content management and leverage technology globally for Regulatory international business functions? Did you always think "there must be a better way" when considering technology in content authoring and content management? Do you want to "break the mold" and...

For one of our international well-known Swiss pharmaceutical clients we are looking for a highly motivated Associate Clinical Trial Supply Manager (m/w/d) in Basel. **Your Responsibilities** - Represent GCS(Global Clinical Supply) as a core member in the integrated Clinical Trial Team (iCTT); define and advise the iCTT on the optimal clinical trial supply...

We are looking for a Clinical Development Medical Director (CDMD) who is responsible for leading the strategic planning and management of the assigned clinical programs from an end-to-end clinical development perspective. As the CDMD, you will oversee the clinical development of the assigned programs and drive the implementation of the clinical development...