As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Clinical Research Associate 作为临床监查员，您将加入全球最大、最全面的临床研究机构 - ICON 临床监查员

Senior Statistical Programmer  Location: Bangalore/Chennai/Trivandrum-Hybrid   ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and...

The Sr. Study Start-Up Associate (Sr. SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements. At the Senior level, the Study Start Up Associate will manage and lead all activities listed above and will ensure that all activities meet Sponsor and PRA expectations and are delivered in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.

As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. CTA Shanghai office based

As a Senior Clinical Data Coordinator (Sr CDC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Workingwithinoneofournewestpartnershipsyou

As a Senior CTA,  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As an Oversight Monitor, Sponsor dedicated you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working as a Contracts Associate you will negotiate contracts and budgets with clinical sites across Germany. We are searching for a professional who has already direct experience in both contract negotiation and managing clinical research budgets with sites. Your responsibilities would also include reviewing the legal wording of the clinical site contracts and so any prior experience in legal or contract writing would be nice to have.  

Working as a Contracts Associate you will negotiate contracts and budgets with clinical sites across Germany. We are searching for a professional who has already direct experience in both contract negotiation and managing clinical research budgets with sites. Your responsibilities would also include reviewing the legal wording of the clinical site contracts and so any prior experience in legal or contract writing would be nice to have.  

As a Local Study Associate Director, you will be leading the Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents and international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), as the Local Study Associate Director (LSAD) you may perform site monitoring as needed to support the flexible capacity model.

As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise to support execution of the clinical studies.   ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to...

As a CTA  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

The SrClinical Research Associate (Sr CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

The role holder will provide a confidential, proactive and highly professional personal service to contributes to operational procurement activities, carrying out sourcing and supplier management activities. A key element of this role is the coordination of Purchase To Pay (P2P) activities between the Procurement Teams and the Accounts Payable or Purchase To Pay Department. Develop internal and external relationships with suppliers and cross-functional teams support in reviewing supplier samples and/or demonstrations with the buying organisation management and user departments.  This Transaction Assistant role will report...

As a Senior Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Senior Statistical Programmer I you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Senior Statistical Programmer Location: Bangalore-Homebased   As a Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.