Clinical Specialist

**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...

**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...

**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 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...

About IQVIA Argentina">We are recruiting talented Medical Science Liaisons to join a dynamic team dedicated to supporting an oral treatment for Multiple Sclerosis (MS). Our team is focused on advancing scientific understanding and building meaningful relationships in the healthcare community.Key Responsibilities:Bridge the gap between cutting-edge science...

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** 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...

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;...

About AQEMIA AQEMIA is a next-gen pharmatech company generating one of the world's fastest-growing drug discovery pipeline. Our mission is to design fast innovative drug candidates for dozens of critical diseases, such as immuno-oncology. Our unique approach leverages quantum-inspired physics algorithms to power generative AI in designing novel drug...

**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. 1-year Fixed Term role **Essential Functions** -...