[Hiring] Senior CRA/CRA II in oncology trials @Syneos Health

Role Description

For one of our clients we are looking for a well-qualified CRA with a strong background in oncology clinical trials across all phases of development, including early phase/first in human studies, safety, PK/PD, and dose escalation designs.

• The ideal candidate will have hands-on experience supporting solid tumor indications such as melanoma, breast, ovarian, prostate, and lung cancer.
• Comfortable operating in fast-paced development environments where quality execution supports accelerated timelines and regulatory submissions.
• Prior exposure to investigational products involving Toll Like Receptor (TLR) pathways, PARP1 inhibitors, or Werner helicase protein is desirable but not required.
• This role requires demonstrated proficiency in traditional on-site monitoring models, including full source data verification, investigational product accountability, and strict adherence to ICH/GCP and regulatory requirements.
• Proven track record of managing visit activities efficiently while producing accurate, comprehensive, and timely monitoring visit and trip reports.
• Extensive experience working within CTMS platforms such as Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or similar systems is expected.
• Multilingual capabilities, particularly fluency in English and German, are strongly preferred.
• Successful candidates will bring a mission-driven and intellectually curious mindset, with a strong sense of ownership and a collaborative, adaptable approach to clinical operations.
• We value individuals who demonstrate professionalism, attention to detail, reliability, and ethical decision-making, along with strong communication and teamwork skills.
• The ability to thrive in a high urgency environment, leverage digital tools effectively, maintain a customer-focused approach with sites and stakeholders, and proactively identify and resolve issues is essential to ensuring trial integrity and success.

Qualifications

• Oncology Expertise: all phases of development
• Indication-Specific Knowledge: solid tumor
• Traditional Monitoring Model: Solid skills and proficiency in on-site monitoring, full source data verification, IP accountability, and regulatory compliance.
• Trip Report Writing: Proven track record in producing accurate, comprehensive, and timely monitoring visit reports, with extensive experience using any CTMS platform (such as Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or similar systems)
• Additional Skills: multilingual - English and German

Requirements

• Mission-focused & intellectually curious: a collaborative mindset with a passion for pushing boundaries and tackling complex challenges to create solutions that matter.
• Collaborative and adaptable mindset: strong professionalism (ethics, detail focus, reliability) with excellent collaboration (communication, teamwork, building trust) and adaptability to a fast-paced environment (sense of urgency for the mission), emphasizing quality, digital fluency (CTMS, eTMF, remote tools) and customer service to sites and sponsors, all while maintaining a proactive, problem-solving mindset to ensure trial integrity and success.

Benefits

• 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 building an inclusive culture – where you can authentically be yourself.
• We are continuously building the company we all want to work for and our customers want to work with.