Regulatory Start Up Intern

The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. To be part of the Regulatory & Start-Up team will help them to decrease the site activation time and help the site to be ready to recruit patients faster. We seek...

**Job Overview** Perform tasks at a country level associated with Site Activation (SA) 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,...

**Who We Are** At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward - always pushing ourselves to go further in our efforts to build a more equitable, inclusive world for our employees, our customers and our communities. **The...

Technology related sales or business development experience - Ability to build and deliver against a plan for your territory which meets or exceeds revenue targets - Entrepreneurial “builder” mentality - Excellent French & English verbal and written communication skills - Comfortable delivering results amid ambiguity and change As a Startup Account...

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...

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...

**CRA Internship - Office Based Paris** **IQVIA Offers fantastic opportunity for students 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 procedures, good...

**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 Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

**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...