Clinical Trial Assistant

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Senior Clinical Research Physician (Senior Clinical Research Medical Manager), GCF 6We are building upon our solid oncology foundation and long-term commitment to patients by developing a whole new class of novel molecules as well as Other therapeutic area, Cardiology and Inflammation – and we need top talent to ensure these molecules become medicines and...

Senior Clinical Research Physician (Senior Clinical Research Medical Manager), GCF 6We are building upon our solid oncology foundation and long-term commitment to patients by developing a whole new class of novel molecules as well as Other therapeutic area, Cardiology and Inflammation – and we need top talent to ensure these molecules become medicines and...

Senior Clinical Research Physician (Senior Clinical Research Medical Manager), GCF 6 We are building upon our solid oncology foundation and long-term commitment to patients by developing a whole new class of novel molecules as well as Other therapeutic area, Cardiology and Inflammation – and we need top talent to ensure these molecules become medicines...

 Are you passionate about driving clinical trials and providing medical expertise? Are you a seasoned medical professional with expertise in clinical trials and therapy areas such as Cardiovascular disease, Chronic Kidney Disease, Liver Disease, inflammation, Alzheimer’s disease, and emerging therapy areas? If so, we have an exciting opportunity for you...

Job Overview Serve as Data Operations Coordinator (DOC)  Essential Functions • Manage delivery of projects through full data management study life-cycle (with minimal guidance). • With guidance from DTL or Manager, manage project timelines and quality. • Determine resource needs. • Identify out-of-scope work. • Serve as Data Operations...

Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Work with sites to adapt, drive and track subject recruitment plan in line...

Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Work with sites to adapt, drive and track subject recruitment plan in...

Job Overview Perform monitoring and site management work for a variety of protocols, site and therapeutic areas. Qualifications • CRA 0.5FTE + Local PM 0.5FTE • Minimum 1 years of PM experience required • Oncology experience preferred • Strong communication skills in English both written and verbal Essential Functions • Perform site...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

 Are you looking for an opportunity where you can utilize your medical knowledge to convey scientific data and interact with medical global thought leaders? Are you highly motivated by being able to make a difference in improving patients’ lives? If so, we have an exciting Clinical Development Center (CDC) Project Manager opportunity for you. Apply...

Description The Opportunity The Clinical Team Lead (CTL) is responsible and accountable for the driving the delivery of the clinical deliverable, acting as the Clinical Project Management (CPM) role within the Core Team. The successful candidate will have overall responsibility of management, co-ordination and administration of our clinical trials...

Description The Opportunity The Clinical Team Lead (CTL) is responsible and accountable for the driving the delivery of the clinical deliverable, acting as the Clinical Project Management (CPM) role within the Core Team. The successful candidate will have overall responsibility of management, co-ordination and administration of our clinical trials and...

Description The Opportunity The Clinical Team Lead (CTL) is responsible and accountable for the driving the delivery of the clinical deliverable, acting as the Clinical Project Management (CPM) role within the Core Team. The successful candidate will have overall responsibility of management, co-ordination and administration of our clinical trials...

Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with...

Typical Accountabilities: Contributes to the selection of potential investigators. In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper...

Job Overview • Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. • Serves as a Lead Medical Writer for late phase studies of Real-World Solutions team. Prepares assigned documents in accordance with IQVIA Standard Operating...

JOB PURPOSE To engage and build strong links with key external medical experts, through developing and maintaining an in-depth understanding of the therapy area and communicating and discussing both the depth of science behind GSK’s Respiratory product and the brand strategies RESPONSIBILITIES Interaction with Medical and Scientific Community ...

JOB PURPOSE To engage and build strong links with key external medical experts, through developing and maintaining an in-depth understanding of the therapy area and communicating and discussing both the depth of science behind GSK's Respiratory product and the brand strategies RESPONSIBILITIES Interaction with Medical and Scientific Community Provide a...