Senior Clinical Research Associate I

🔥 12 hours ago

🇩🇪 Germany – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

infoinfo

🗣️🇩🇪 German Required

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of Pfizer

Pfizer

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• Independently manage and monitor assigned investigational sites throughout the entire study lifecycle • Ensure compliance with ICH-GCP, regulatory requirements, and internal quality standards • Conduct Site Initiation Visits, Monitoring Visits, and Close-Out Visits (onsite and remote) • Build and maintain trusted relationships with investigators and study staff • Support patient recruitment, study activation, and data quality • Identify and resolve study-related challenges and implement corrective and preventive actions • Support audits and inspections, as well as quality initiatives • Mentor and provide subject-matter support to Clinical Research Associates

🎯 Requirements

• Bachelor’s degree in Life Sciences or an equivalent qualification (e.g., nursing, pharmacy, or a medical background) • At least 3 years of experience in clinical monitoring • Oncology experience preferred, along with knowledge of additional therapeutic areas such as vaccines, internal medicine, or infectious diseases • Strong knowledge of ICH-GCP and national and international regulatory requirements • Experience with global clinical trials • Excellent written and spoken German and English • Strong communication, organizational, and problem-solving skills • Willingness to travel approximately 60–80% within Germany and, where applicable, internationally • Valid driver’s license and passport required

🏖️ Benefits

• Pfizer guarantees equal opportunities throughout the entire application process • Inclusive employer committed to equal opportunities for all applicants • Reasonable accommodations for applications and future careers • Accessibility assistance for the website, online application process, and interviews

Apply Now

Similar Jobs

🕒 4 days ago

Syneos Health

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Clinical Trial Manager overseeing site management, monitoring, compliance, and risk for Syneos Health’s sponsor-dedicated trials in Germany. Coordinating CRAs, study teams, systems, and milestones.

🕒 August 25

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Senior Clinical Research Associate overseeing oncology and Phase I trial monitoring for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol compliance, data integrity, and site performance.

🗣️🇩🇪 German Required

🕒 August 18

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Senior Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence organization. Ensuring site compliance, data integrity, and successful trial execution across Germany.

🕒 August 17

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate monitoring and managing phase II–IV clinical studies for ICON, a global healthcare intelligence and clinical research organisation. Ensuring ICH-GCP compliance, regulatory submissions, site oversight, and study documentation.

🗣️🇩🇪 German Required

🕒 August 13

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Site Engagement Liaison building clinical trial site relationships for ICON, a global healthcare intelligence and clinical research organisation. Supporting study compliance, engagement strategies, and site performance.