Clinical Trials Assistant

**Clinical Trial Manager** Global or Regional Applicability: Regional Trial Management services provide local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to-end project management from...

External Job Description This role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. Assist with daily workload planning. **Trial and site administration**: - Manage SIP, Track (e.g. essential documents) and report (e.g. Safety Reports) - Ensure collation and...

**Join us in our exciting journey!** We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials Coordinator. Our client is one of the TOP 5 pharmaceutical companies who is dedicated and passionate about improving the lives of patients across several therapeutic...

**Join us in our exciting journey!**: We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials Coordinator. Our client is one of the TOP 5 pharmaceutical companies who is dedicated and passionate about improving the lives of patients across several therapeutic...

Provide global, regional or complex local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to[1]end project management including start-up, execution, close-out, analysis and reporting. Further,...

Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions - Complete appropriate therapeutic, protocol and clinical research...

**Job Overview** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Fluent in French and English.** **Essential Functions** - Oversee the execution of Site Activation...

**CRA Internship - Office Based Paris** **IQVIA Offers fantastic opportunity for Graduates and Professionals who wish to become a CRA.** By joining IQVIA as CRA Intern you will engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating...

This role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. Assist with daily workload planning. This is a **Hybrid** role - office based in **Paris** **Trial and site administration**: - Manage SIP, Track (e.g. essential documents) and report (e.g. Safety...

**Medical Science Liaison - Oncology - France / Belgium** IQVIA is looking for an MSL (Medical Scientific Liaison) based in France to join our client’s global oncology team as they prepare for launch of a next generation TKI for kidney, metastatic colorectal and head & neck cancers. **_ Responsibilities:_** - Provide field-based medical support to the...

Job Overview 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 Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

Job OverviewProject 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 Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

Due to our continued growth, we are recruiting for a Sr. Clinical Research Associates to join our team. This is a great opportunity for a CRA to join a progressive and developing CRO.IQVIA Biotech is unique division specialising in working with smaller biotech and emerging biopharma clients, and as such we have a vibrant, fast-paced working environment....

**Clinical Specialist - Wound Closure (orthopedic focus) - South East France** As part of a team expansion project across the EU including Netherlands, Italy, Germany, and the UK, IQVIA is recruiting for 2 field-based Clinical Specialist positions in France, on behalf of our client - a highly respected global company renowned for its innovation and success...

**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. This role requires fluency in the English language. **Essential Functions** - Perform site monitoring visits (selection,...

**Job Overview** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Hybrid - in office 3x a week.** **Essential Functions** - Oversee the execution of Site Activation...

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 accordance with contracted...

Our unique approach leverages quantum-inspired physics algorithms to power generative AI in designing novel drug candidates—without relying on experimental data. The Early Asset Valuation Specialist will provide competitive intelligence lead for internal assets and synthesize data into actionable insights. Analyse clinical trial data, regulatory pathways...

Job Overview 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 Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions - Under general supervision,...