Clinical Research Associate (m/f/d)

TFS HealthScience; Hamburg; Teletrabalho; EUR 42 000 - 64 000; Tempo integral

Resumo da oferta

TFS HealthScience is seeking a Clinical Research Associate to join our CDS Oncology team from home in Germany. You will monitor trials, ensure data integrity, and support regulatory compliance while collaborating with sites and sponsors.

This role requires life science or nursing background, GCP/ICH knowledge, fluent English and German, and willingness to travel up to 60-80% to sites and meetings.

Qualificações

• Bachelor's Degree in life science or nursing (or equivalent).
• Over 1 year of relevant clinical experience in trials or development.
• Understand GCP/ICH guidelines and regulatory requirements.
• Strong written and verbal communication skills in English and German.

Responsabilidades

• Monitor on-site and remote trials in accordance with GCP/ICH and SOPs.
• Verify informed consent procedures and protocol compliance.
• Review CRFs and source documentation for accuracy.
• Verify management of Investigational Product and related records.
• Timely reporting of monitoring findings and CAPAs.
• Update CTMS and site documentation; support audits/inspections.

Conhecimentos

GCP & ICH knowledge

Study monitoring

Data integrity

Communication skills

Fluent English & German

Travel readiness

Formação académica

Bachelor's degree in life sciences or nursing

Descrição da oferta de emprego

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a Clinical Research Associate - home based in Germany (Hamburg area preferred).

About This Role

As part of our CDS Oncology team you will be working alongside passionate and innovative professionals to ensure our customers achieve their goals.

Key Responsibilities

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations. Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
• Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
• Review CRFs (electronic or paper) and subject source documentation for validity and accuracy
• Verify proper management and accountability of Investigational Product.
• Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escape observed deficiencies and issues as appropriate.
• Providing site with the listing of issues identified during monitoring visit and action items which will need to be addressed in a timely manner.
• Timely delivering site documents to eTMF or paper TMF; verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and ICH guidelines and local regulatory requirements.
• Participate in audit and/or inspection, its preparation and follow-up activities, as needed.
• Order, ship, and reconcile clinical investigative supplies for study sites, if applicable
• Update CTMS and all other required by projects systems with accurate site level information

Qualifications

• Bachelor's Degree, preferably in life science or nursing; or equivalent
• Over 1 year of relevant clinical experience or relevant academic background around clinical trial or clinical development activities
• Able to work in a fast-paced environment with changing priorities.
• Understand basic medical terminology and science associated with the assigned drugs and therapeutic areas.
• Possess the understanding of Good Clinical Practice regulations, ICH guidelines.
• Ability to work independently as well as in a team matrix organization.
• Strong written and verbal communication skills.
• Fluent in English and German
• Excellent organizational skills
• Technology savvy and good software and computer skills
• Soft skills: Self-awareness, resolute, flexibility, proactivity, collaborative mindset, analytic approach, and attention to detail
• Ability and willingness to travel up to 60-80%, overnight and abroad if applicable.

What We Offer

We provide a competitive compensation package, comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration.

Together we make a difference.