Site Start Up
hace 4 días
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We’re looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trials?
**Key Responsibilities**
- Support SSU team in executing clinical trial start-up activities within timelines.
- Assist in drafting and reviewing start-up documents and study plans.
- Prepare reports, meeting minutes, presentations, and track documents.
- Document and escalate study-related issues to the appropriate manager.
- Act as a system/process expert, ensuring compliance and efficiency.
- Maintain training records and attend required internal/external training.
- Participate in process improvement initiatives across departments.
**Education**
- Bachelor’s degree required, preferably in Life Sciences or a related field.
- 1 year experience in clinical research (Sponsor, CRO, Vendor, or Clinical Coordinator role).
- Proficient in Microsoft Teams, Word, Excel, PowerPoint, Outlook, and SharePoint.
- Self-motivated with strong time management and ability to meet deadlines.
- Excellent communication & collaboration skills in a fast-paced environment.
Join Fortrea and be part of a dynamic team driving clinical research forward. If you're eager to grow, thrive in a fast-paced environment, and want to make a real impact, we’d love to hear from you
**Fortrea is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Start-Up, Project Manager
hace 2 semanas
Madrid, Madrid, España Indero (formerly Innovaderm) A tiempo completoThe Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and collaborates with cross-functional teams to meet study timelines and client expectations. The ideal candidate will bring strategic...
-
Start Up Specialist
hace 5 días
Madrid, Madrid, España Fortrea A tiempo completoJoin Our Team and Drive Clinical Research SuccessAt Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will...
-
Global Start Up Assistant
hace 2 semanas
Madrid, España Allucent A tiempo completoAt 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 Global Start-Up Assistant to join our A-team! The Global Start-up Assistant (GSUA) provides administrative support to all...
-
Study Start Up Manager
hace 6 días
Madrid, España Ergomed A tiempo completoCompany Description Ergomed is a rapidly growing global clinical research company. We perform clinical trials for rare and complex diseases. Ergomed Plc is a public company on the London stock exchange. The company boasted 40% growth in its revenues in its last report. This success is due to the hard work of our highly skilled employees and our subsequent...
-
Study Start Up Lead
hace 3 días
Madrid, España Roche A tiempo completoThe Position At Roche / Genentech Pharma Product Development Global Clinical Operations (PDG) we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029. As a key member of our Country Study Start‑Up team you will drive and facilitate...
-
Start Up Specialist
hace 2 semanas
Madrid, España Fortrea A tiempo completoStart Up Specialist / Site Readiness and Reg Specialist II - FSPx Team - SpainFortrea, Madrid, Community of Madrid, SpainJoin Our Team and Drive Clinical Research Success!At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start‑Up Specialist, you will play a pivotal role in coordinating site...
-
Senior Oncology Study Start-Up Specialist
hace 1 día
madrid, España Kapadi A tiempo completoA clinical research organization is seeking a Clinical Research Associate III in Madrid to handle study start-up and maintenance for oncology trials. The role involves managing site activities, maintaining compliance with regulations, and coordinating with project teams. Candidates should have a Bachelor's Degree in a relevant field, with over 5 years of...
-
Senior Manager, Study Start Up
hace 6 días
Madrid, España ICON plc A tiempo completoICON 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...
-
Madrid, España Kapadi A tiempo completoA leading clinical research organization in Madrid is seeking a highly-motivated Clinical Research Associate III to manage study start-up and maintenance activities. The successful candidate will ensure compliance with regulatory requirements, support site activation processes, and coordinate with project teams. Required qualifications include a Bachelor's...
-
Senior Regulatory
hace 2 semanas
Madrid, España IQVIA A tiempo completoJob 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, serve as...