Clinical Research Associate / Senior Clinical Research Associate at PSI CRO

Munich, Bavaria, Germany -

Full Time

Start Date

Immediate

Expiry Date

12 Aug, 26

Salary

0.0

Posted On

14 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

On-site Monitoring, Remote Monitoring, CRF Review, Source Document Verification, Query Resolution, Site Management, Site Identification, Clinical Trial Monitoring, MS Office, Problem Solving, Collaboration, Multitasking

Industry

Pharmaceutical Manufacturing

Description

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Hybrid role in Munich/Planegg or Home-based in Germany You will: Conduct and report all types of onsite monitoring visits as well as remote visits. Perform CRF review, source document verification and query resolution. Be responsible for site communication and management. Be involved in site identification process. Assist in training of less expert CRAs, depending on your level of experience. Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience. Independent on-site monitoring experience in Germany. Experience in Switzerland is a plus. Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III. Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus. Full professional proficiency in German and English. French language skills are an asset. Advanced proficiency in MS Office applications (Word, Excel, PowerPoint, Outlook). Ability to plan, multitask and work in a dynamic team environment. Communication, collaboration, and problem-solving skills. Ability to travel and valid driver’s license. Additional Information As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. With no investors to please, our management focuses on company culture and operational delivery over quarter-to-quarter profitability. Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success. Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you: Excellent and flexible working conditions. A unique combination of team collaboration and independent work. Competitive salary and benefits package. If you'd like to hear more about PSI, our organic growth and company culture, and learn more about the studies that we run and our high repeat and referral business rates, please apply for this vacancy.

Responsibilities

The role involves conducting and reporting onsite and remote monitoring visits for clinical studies across various therapeutic indications. Responsibilities include CRF review, source document verification, and managing site communications and identification.