Sponsor Dedicated Senior CRA - Switzerland (German, French and Italian speaking)

Syneos Health; Zurich; On-site; CAD 80,000 - 110,000; Full time

Job summary

A leading biopharmaceutical organization is seeking a Senior Clinical Research Associate in Switzerland, fluent in German, French, and Italian. The ideal candidate will leverage their experience in oncology monitoring to manage clinical trials while ensuring compliance with regulatory standards. Join a passionate team dedicated to accelerating therapy delivery and making a tangible impact in healthcare.

Benefits

Career development and progression

Total rewards program

Supportive line management

Qualifications

• On-site monitoring experience in clinical trials.
• Strong Oncology experience in phases 1-3.
• Fluency in English and local languages (German, French, Italian).

Responsibilities

• Assess qualifications of clinical study sites.
• Implement and manage clinical studies.
• Ensure compliance with GCP and protocols.

Skills

Monitoring skills

Analytical skills

Interpersonal skills

Problem-solving

Education

BA/BS in Life Sciences or RN

Tools

Microsoft Office

EDC, IVRS, CTMS systems

Job description

Sponsor Dedicated Senior CRA - Switzerland (German, French and Italian speaking)

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Description

Sponsor Dedicated Senior CRA - Switzerland (German, French and Italian speaking)

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 brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate 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. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
  
  

Job Responsibilities

The primary responsibilities of this position include assessing qualifications of potential clinical study sites, implementing clinical studies at participating sites, managing the conduct of clinical studies at sites, ensuring the quality of site performance, and closing clinical studies. This individual will ensure that clinical trials are conducted according to the approved protocol/protocol amendments and comply with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirements. The Senior CRA is a seasoned professional with wide-ranging experience and a thorough understanding of GCP and ICH principles. The experienced Senior CRA identifies and resolves complex issues where an analysis of situations and data requires an in-depth evaluation of multiple factors. Exercising sound judgement in selecting methods and techniques and evaluating criteria for resolving issues, the Senior CRA will establish strong, positive relationships with both internal and external partners. This individual contributes to the determination, development and/or implementation of efficient and effective approaches to study site management.

Qualifications: Position requires BA/BS preferably in the Life Sciences, or RN, Solid on-site monitoring experience gained from pharmaceutical / biotechnology industry monitoring as a Clinical Research Associate from study start-up to database lock. Strong Oncology monitoring experience in phase 1-3 pharmaceutical/ biotechnology clinical trials. Demonstrated high level of monitoring skill with independent professional judgment. Possess excellent understanding and working knowledge of ICH guidelines, Good Clinical Practices (GCP), PhRMA code, FDA CFR, clinical research ethics, HIPAA and patient privacy laws, and other relevant, local regulatory requirements. Strong knowledge of concepts of clinical research and drug development. Strong working knowledge of EDC, IVRS and CTMS systems. Proficient in the use of Microsoft Office. Ability to work highly independently across multiple studies, projects and sites. Ability to work effectively in a team/matrix environment. Ability to understand technical, scientific and medical information. Demonstrated strengths in planning, organizational, project management, analytical, oral and written communication, effective time management, conflict management, problem solving, attention to detail, and interpersonal skills Demonstrated ability to mentor/lead Works with high quality and compliance mindset Possess a valid driver’s license Must be willing to travel and spend 8-10 days /month on site. Proficient in speaking and writing English and the local country languages, Germany, French and Italian.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all 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 the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

We are searching for CRA in Switzerland with experience on early oncology and able to monitor in German, French and Italian and is fluently in English.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research and Science

• Industries

  Biotechnology Research, Pharmaceutical Manufacturing, and Research Services

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