CRA Contractor Germany

Overview

CRA Contractor Germany — Freelancer on a six-month contract. For our team in Germany we monitor a variety of trials, including some real world evidence studies.

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model centers on the customer and patient, aiming to simplify and accelerate delivery of therapies to change lives.

Discover what our 29,000 employees across 110 countries already know: WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture where you can authentically be yourself and feel you belong.
• We value diversity of thoughts, backgrounds, cultures, and perspectives to create an inclusive workplace.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices, verify data accuracy and completeness, and ensure adherence to study protocols.
• Develop and implement tools, procedures, and processes to ensure quality monitoring, including standardized templates for monitoring reports and site-visit checklists.
• Contribute to design, implementation, and delivery of processes, programs, and policies; participate in development of clinical trial protocols and provide input on study design and methodology.
• Manage and direct work of junior staff or oversee day-to-day activities of clinical trial sites; provide guidance and support as needed.
• Ensure accurate and timely documentation and reporting of clinical trial data; maintain detailed records of site visits and monitoring activities; prepare reports for regulatory submissions.
• Collaborate with cross-functional teams (data management, biostatistics, regulatory affairs) to ensure successful trial execution.
• Identify and resolve issues related to trial conduct and data integrity; troubleshoot data collection problems and discrepancies in study records.
• Provide training and mentorship to junior staff on monitoring techniques and best practices.

Qualifications

• Bachelor's degree in a related field
• Minimum of 3-5 years of experience in clinical research or related field
• In-depth knowledge of clinical trial processes and regulations
• Fluent in German
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team

Necessary Skills

• Proficiency in clinical trial management systems and software
• Strong organizational and time management skills
• Attention to detail and accuracy
• Ability to manage multiple projects and priorities simultaneously
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter what your role is, you’ll take initiative and challenge the status quo in a dynamic environment. Learn more about Syneos Health.

Additional information:

Equal Opportunity Employer

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at