Regulatory Start-Up/Site Activation Specialist- Home-Based In Spain

Regulatory Start-up/Site Activation Specialist- home-based in Spain page is loaded Regulatory Start-up/Site Activation Specialist- home-based in Spain Apply locations Madrid, Spain Barcelona, Spain time type Full time posted on Posted 2 Days Ago job requisition id R Essential Functions Under general supervision, serve as Single Point of Contact (SPOC) in...

ob OverviewPerform 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. At least 1 years' experience with submissions and CTIS...

Job OverviewDirect 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 Spanish and English.Essential Functions Oversee the execution of Site Activation (including...

Job OverviewDirect 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 Spanish and English.Essential Functions Oversee the execution of Site Activation (including...

QualificationsBachelor's Degree Related field2 year clinical research experience. Equivalent combination of education, training and experience.In-depth knowledge of clinical systems, procedures, and corporate standardsStrong knowledge of medical terminology and regulationsBroad knowledge of clinical researchStrong knowledge of Microsoft Office and e-mail...

Job OverviewUnder 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; maintains,...

Job OverviewUnder 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; maintains,...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development...

Job OverviewDirect 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.Essential Functions Oversee the execution of Site Activation (including preaward/bid defense activities) and/or...

Overview:Join us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

Qualifications Bachelor's Degree Related field 2 year clinical research experience.Equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards Strong knowledge of medical terminology and regulations Broad knowledge of clinical research Strong knowledge of Microsoft Office and...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Local Start Up Senior Specialist (LSUS) to join our A-team (hybrid*/remote) The Local Start-up Senior Specialist (LSUS)...

CATO SMS and Pharm-Olam, LLC have merged to form AllucentThese customers have new therapeutic ideas but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You'll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately,...

Due to our continued growth Precision for Medicine are hiring an experienced Manager/Senior Manager, Site Start up to join our team to line manage our team of Start up Leads in the EU/UK. Candidates can be based in Spain, Hungary, Slovakia, Serbia, Romania, Poland or UK.Position Summary: Manages and oversees the day-to-day activities SSU personnel in...

At AllucentTM, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Local Start Up Specialist I/II (LSUS) to join our A-team (hybrid*/remote) The Local Start-up Specialist (LSUS) coordinates and...

Due to our continued growth Precision for Medicine are hiring an experienced Manager/Senior Manager, Site Start up to join our team to line manage our team of Start up Leads in the EU/UK. Candidates can be based in Spain, Hungary, Slovakia, Serbia, Romania, Poland or UK.Position Summary:Manages and oversees the day-to-day activities SSU personnel in...

Company DescriptionOur client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Start up Manager home based in SpainJob OverviewLeading cross-functional project teams...

Job Description**Please note this role can be based remotely from locations across SpainThe Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local...

These customers have new therapeutic ideas but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You'll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you'll help make a positive difference in patients'...

Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation. Job Description - Brand Activation Specialist-Neutrogena - Maternity Leave W) Brand Activation Specialist-Neutrogena - Maternity Leave W Description Kenvue is currently recruiting for a Brand Activation Specialist - Neutrogena to cover a...