As a Inhouse Clinical Research Associate you will be expected to provide clerical support to project team during the study conduct, assist in regulatory submission and Clinical Research Associate activities at the study start and perform other administrative duties as assigned by management.

Reporting to the Senior Clinical Operations Manager , you will be an important member of the Clinical Operations team in Germany.

We are searching for an ambitious and energetic person, able to undertake challenges in the projects.

We ensure detailed training in the job responsibilities and on the job support and mentoring as well as possibility for further development and career advancement in our growing company.

Minimum Qualifications & Experience:

• Excellent written and oral communication skills in English and German
• Excellent organizational and time management skills
• Openness to learn new things and communicate across countries and cultures
• Attention to detail
• Degree in life sciences or related allied health profession (e.g. nursing certification, medical or laboratory technology)
• Previous experience in clinical research field will be additional advantage.

Job Responsibilities:

• Providing clerical support to project team (e.g., word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
• Assisting in submission and other Clinical Research Associate activities e.g. compiling of regulatory packages, translation of clinical documents, updating trackers, assisting in feasibility
• Setting up and maintaining clinical investigator files and documentation in-house and on-site
• Preparing investigator budget payments and tracking systems; generating tracking reports as assigned
• Performing data entry and maintenance of selected study tracking databases
Preparing study-related documents and other materials for delivery to archives, at appropriate intervals

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.