Clinical Research Associate

**About Implantica Group Implantica is a medtech group dedicated to bringing advanced technology into the body. Implantica’s lead product, RefluxStop, is a CE-marked implant for the prevention of gastroesophageal reflux that will potentially create a paradigm shift in anti-reflux treatment as supported by successful clinical trial results. Implantica also...

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

Social network you want to login/join with:ResponsibilitiesCoordinates investigator/site feasibility and identification process, as well as study startup.Monitors project timelines and patient enrollment, implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting compliance of the...

Job Description Coordinates investigator/ site feasibility and identification process, as well as study startup. Monitors project timelines and patient enrollment, implements respective corrective and preventive measures. Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region. Manages...

If you are currently performing the role for a Clinical Trial Manager or Clinical Operations Manager and looking to step into a Director position this is your chance! My Client who is an international company is looking for a Associate Director - Clinical Operations to join their team in the office in Zug, Switzerland on a 12 month contract. They are focused...

The Senior Clinical Project Manager/Associate Director, Clinical Operations will provide operational expertise within the Research and Development function to ensure timely initiation, execution and reporting of clinical trials in accordance with ICH/GCP and all applicable requirements (including local regulations) to support licensure of products in the...

Social network you want to login/join with:ResponsibilitiesWrites, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation.Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives.Collects and tracks documents for CSR...

Job Description Writes, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives Collects and tracks documents for CSR appendices, in support of the Quality Control...

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 the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved in data...

Proclinical are recruiting a Clinical Scientist for a pharmaceutical organisation. This role is on a contract basis and is located in Europe. The client is focused on providing life changing remedies for various illnesses. **Responsibilities**: - To increase quality and effectiveness, you will guarantee consistent improvement of medical and scientific...

Seagen is a global multi-product biotechnology company that develops and commercializes innovative therapies for the treatment of cancer. The company’s industry-leading antibody-drug conjugate (ADC) technology harnesses the targeting ability of antibodies to deliver cell-killing agents directly to cancer cells. In addition to four marketed products, we are...

Proclinical are recruiting a Scientist - Clinical Pharmacology for a pharmaceutical organisation. This role is on a permanent basis with the ability to work remotely from anywhere in Switzerland. The client is focused on developing a new class of novel remedies to change the lives of many. **Responsibilities**: - Guide the analysis, interpretation,...

**Position Description**: **Primary Responsibilities**: - The Director, Clinical Monitoring will be responsible for all aspects of monitoring and site management oversight for all of Urovant's CRO partners. He/she will work closely with Urovant's Clinical Operations Leads, Data Management, and QA, as well as with all involved functions and vendors (such as...

Johnson & Johnson MedTech Companies are committed to reaching more patients and creating a better quality of life. The J&J Companies have been advancing patient care for more than a century. With an unparalleled range of products and services, programs, and research and development in surgical technologies, orthopedics, cardiovascular and specialty...

For our client in Zug we are lookig for a **Clinical Development Leader (M/F/d)**: - Location Zug - Contract type temporary contract - Start/End: ASAP - 1 year with extension You will provide clinical expertise in heart failure care for the medical value innovation pipeline of novel diagnostic solutions and disease management solutions. In close...

**About Us** Urovant Sciences, Inc. is a biopharmaceutical company focused on developing and commercializing innovative therapies for urologic conditions beginning with overactive bladder. Our lead product, GEMTESA®(vibegron), is an oral, once-daily tablet for the treatment of adult patients with overactive bladder (OAB) with symptoms of urge urinary...

Local Clinical Operations Manager - Schweiz (für Global Clinical Operations Janssen D-A-CH) Über Johnson & Johnson - Janssen Seit über 130 Jahren gehören Diversity, Equity & Inclusion (DEI) zu unserer Unternehmenskultur bei Johnson & Johnson. Sie sind ein Grundprinzip unseres täglichen Handelns. Die Würde und Vielfalt aller Menschen zu respektieren,...

Site Name: UK - Hertfordshire - Stevenage, GSK HQ, Upper Providence, USA - Massachusetts - Waltham, Warsaw Rzymowskiego 53, Zug HousePosted Date: Dec 4 2024Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you!As...

Position Summary: - Up, to define vision, goals, strategies and tactics to ensure delivery of study start-up activities per project plans across the portfolio. The Associate Director will lead and a team of SSU managers to drive site activation delivery focused on quality, efficiency and expediency. This role is responsible for performance management of...

Clinical Project Physician (Rheumatology/Autoimmune) – Based Anywhere in Europe (m/w/d)Client: ViatrisLocation: ZugJob Category: OtherJob Reference: 1c8881bda3a6Job Views: 15Posted: 21.01.2025Expiry Date: 07.03.2025Job Description:At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source...