Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor

Standort:

• Frankfurt am Main

Zusammenfassung

• Arbeitszeit: Vollzeit
• Typ: Festanstellung
• Qualifikationslevel: Spezialisierungsformen und Funktionen

Gewünschte Fähigkeiten & Kenntnisse

• Integrity
• Pace
• START
• Progress
• Mentoring
• Support
• CRF
• Clinical Research Associate
• LESS
• Flexibilität

Unsere Leistungen

• Homeoffice

Stellenbeschreibung

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Ihre Aufgaben

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborating with experts at study sites and with client representatives.
• Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).
• Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.

Ihr Profil

• University Degree in life science or other scientific discipline or apprenticeship in the health care field.
• Minimum of two-four years of on-site monitoring experience alternatively an equivalent combination of education, training and experience.
• Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.
• Fluency in German on at least C1 level and a good command of English.
• Flexibility to travel up to 40-60% of working time.
• Driver's license class B.

Wir bieten Ihnen

• Permanent employment contract.
• Home-office and flexible working schedules.
• Competitive salary
• Company car or car allowance, accident insurance, pension and more.
• Resources that promote your career growth.

Whatever your career goals, we are here to ensure you get there!

Profil

Fachliche Voraussetzung

• Biologie, Coaching und Mentoring, Gute Klinische Praxis, Inspektion vor Ort, Klinische Forschung, Medizinische Versorgung, Medizinisches Material, Prüfbögen, Recruiting, Regulatorischen Anforderungen, Standortauswahl, Veranstaltungsmanagement, Zulassungsanträge

Persönliche Fähigkeiten

• Anpassungsfähigkeit, Detailgenauigkeit, Kommunikation

Sprachkenntnisse

• Deutsch, Englisch

Berufserfahrung

• Mit Berufserfahrung

Bewerbung

Jetzt bewerben

Branche:

IKT

Arbeitgeber:

IQVIA Inc.

Adresse:

IQVIA Inc. 07980 Berga-Wünschendorf

Web:

http://jobs.iqvia.com