Clinical Trials Assistant

Job SummaryThe Clinical Trials Assistant will provide administrative support to the clinical teams at Pharmiweb, helping to ensure the smooth execution of clinical trials. This role is ideal for a highly organized and detail-oriented individual with excellent communication skills.Key ResponsibilitiesAssist clinical teams with updating and maintaining...

**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...

OverviewThe Clinical Trials Assistant will provide administrative support to the clinical research team at Pharmiweb. This role is a key part of our team and will help us deliver high-quality clinical research services to our clients.Key ResponsibilitiesSupport the clinical research team with administrative tasks, including data entry, filing, 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...

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...

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,...

**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...

**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,...

We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join ProductLife Group as a key member of our pharmaceutical team.About the RoleThe successful candidate will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally. This involves...

Strengthen our self-care medical device division by joining our team as a Scientific Affairs Associate for Medical Devices with experience in evaluating the efficacy and safety of health products in the European market.In this role, you'll work closely with Senior Consultants in a small dynamic team, overseeing the entire life cycle of self-care medical...

**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...

We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company, ProductLife Group. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally.Responsibilities:Prepare and...

We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally).Responsibilities:Prepare and...

**Job Overview** 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** -...

**We are growing, grow with us!** Are you looking for a dynamic company with daily new challenges and opportunities? Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any...

**We are growing, grow with us!** Are you looking for a dynamic company with daily new challenges and opportunities? Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any...