Clinical Research Associate

pAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Through our PPD clinical research services, we support clinical trials in more than 100 countries, delivering laboratory, digital and decentralized solutions that help bring life-changing therapies to patients faster.brErfahrung, Qualifikation und Soft Skills, haben Sie alles, was Sie brauchen, um bei dieser Gelegenheit erfolgreich zu sein? Finden Sie es unten heraus.brOur goal-driven teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the world to decrease startup timelines and exceed expectations.brWork on high-quality, global clinical trials across diverse therapeutic areasbrBe part of a stable, well-established organization with long-term career opportunitiesbrStrong collaboration with experienced CTMs and project teamsbrSenior CRA, Lead CRA, CTM)brFlexible working models that support work-life balancebrPermanent employmentbrFull-time (40 hours/week)brThis position is for experienced Clinical Research Associates with 2+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, ICH-GCP, applicable regulations, and company SOPs.brYou'll work autonomously, partner closely with investigative sites, and collaborate with project teams to deliver high-quality, inspection-ready clinical trials.brPerform site monitoring activities (on-site and remote) using a risk-based monitoring approachbrEnsure protocol, ICH-GCP, regulatory, and SOP compliance at investigator sitesbrMaintain ongoing communication with sites between visits to support issue resolution and data qualitybrSupport study start-up, investigator identification, site initiation, and study close-out activities as assignedbrParticipate in investigator meetings, audits, inspections, and project team meetings as requiredbrAdditional responsibilities may include supporting process improvement initiatives, mentoring activities, or project-specific tasks aligned with experience.brConduct on-site or remote monitoring visitsbrCollaborate with CTMs and project teams to keep studies on track and inspection-readybrEducation ExperiencebrBachelor's degree in a life sciences related field or equivalent qualificationbrMinimum 2 + years of experience as a Clinical Research Associate / MonitorbrFluency in German and English (C1 level)
- interviews will be conducted in English GermanbrStrong clinical monitoring skills with hands-on RBM experiencebrSolid therapeutic area knowledge and medical terminologybrStrong written and verbal communication skills with medical professionalsbrFlexibility and adaptability in a dynamic project environmentbrProficiency in Microsoft Office and ability to learn clinical systems (e.g., Locations: Home-based or hybrid anywhere in GermanybrFTE: Full-time (40 hrs/week)brPermanentbrAt PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme , ensuring you reach your potential.brAs well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture , where PPD clinical research services truly value a work-life balance. We are a global organization but with a local feel. xsxvtuf brSchwerbehinderte Bewerberinnen und Bewerber werden bei gleicher Eignung bevorzugt berücksichtigt. /p