Experienced Clinical Research Associate (Sign-On Bonus eligible)
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
- Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Qualifications
- Must have a minimum of a university degree in a health or life science related field;
- Min.1.5 years of previous experience.
- Approximately 60-80% travel in Germany, Austria and Switzerland;
- Proficient knowledge of Microsoft® Office and general computer literacy;
- Outstanding communication and Presentation skills;
- Must be detail-oriented and efficient in time management;
- Excellent verbal and written communication skills in English and German;
- Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities.
Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Sign on Bonus for up to 7.500 EUR based on experience.
Awards
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Empfohlene Jobs
Vertriebsmitarbeiter/in in der Spedition (m/w/d)
Für unseren Standort in München suchen wir Sie zum nächstmöglichen Zeitpunkt als Vertriebsmitarbeiter/in in der Spedition (m/w/d) Ihre Aufgaben als Vertriebsmitarbeiter/in in der Spedition (m/w/…
Key Account Manager (m/w/d) ab sofort (nach Vereinbarung)
+++ DIREKTVERMITTLUNG in Festanstellung (keine Zeitarbeit) / Vermittlungsgutscheine (AVGS) werden akzeptiert - KOSTENPFLICHTIG +++ Bei Fragen einfach unverbindlich anrufen: 03048479484 oder einen R…
Kundendiensttechniker/in (m/w/d)
Diese Tätigkeiten könnten bald Ihre sein: Installation, Wartung & Reinigung von Wasserspendern / Tafelwasseranlagen Reparatur und Sicherstellung der Funktionalität der Wasserspender Technisc…
Einkäufer (m/w/d)
Ihre Aufgaben: Eigenverantwortliche Durchführung des operativen und strategischen Einkaufs Betreuung des gesamten Beschaffungsprozesses - von der Bedarfsermittlung bis zur Rechnungsprüfung …
Raktári munkák Németországban, 12,83-14,00€/h fizetés, szálláslehetőség
Folyamatosan keresünk új munkatársakat németországi hütött élelmiszerraktárakba.Frankfurt, München, Bayreuth, Kassel, Hannover és vonzáskörzetükben találhatók a raktárak.Munkakezdés: folyamatosanFelad…
Lehrkraft Ergotherapie (m/w/d)
Bereit für den nächsten Schritt? Ein Teamwechsel könnte Deine beste Entscheidung sein! Die Döpfer Gruppe - Dein neues Team im Gesundheitswesen.Das Team Döpfer umfasst deutschlandweit ca. 900 Kollegen…
Volljurist:in (m/w/d), Syndikusrechtsanwalt (m/w/d) im Arbeitsrecht
Wir suchen genau DICH! Als inhabergeführtes Unternehmen mit einem klaren Fokus auf innovative Arbeitsstrukturen und wertschätzende Unternehmenskultur gestalten wir nicht nur Räume, sondern auch n…
** Schweinfurt: Lust auf Pizza, gute Laune und Live-Action? 🍕✨**
Kurzfristige Beschäftigung
Principal Product Owner - Supply Chain Automation
At Rohlik, we are on a mission to reinvent the grocery shopping experience, enhancing our customers’ lives by helping them eat and live better. We are Europe's leading online grocery delivery service…
Systemadministrator (m/w/d)
Starten Sie in München als Systemadministrator (m/w/d) bei einem Anbieter von IT Services . Das Unternehmen konzentriert sich auf Managed Services , IT Infrastruktur und Systemintegrati…