Patient Data Specialist

Precision Medicine Group; Tarragona; A distancia; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An innovative company is seeking a Patient Data Specialist to enhance the precision of oncology treatments. This remote role involves reviewing clinical data, ensuring accuracy, and collaborating with cross-functional teams. Ideal candidates will have a background in healthcare or science, with a strong grasp of oncology standards and experience in clinical trials. Join a forward-thinking organization dedicated to revolutionizing cancer treatment through advanced data management and biomarker-driven insights. If you thrive in a dynamic environment and are passionate about improving patient outcomes, this opportunity is perfect for you.

Formación

• Experience in oncology clinical trials, especially hematologic malignancies.
• At least two years in clinical operations or related roles.

Responsabilidades

• Review subject data for accuracy according to oncology standards.
• Support data output development and user acceptance testing.

Conocimientos

Medical terminology

Oncology knowledge

Data management

Problem-solving

Interpersonal skills

Educación

Bachelor’s degree in science or healthcare

Medical degree or relevant healthcare qualification

Herramientas

EDC systems

Data visualization tools

Descripción del empleo

We are seeking a Patient Data Specialist to join our team!

This is a remote-based opportunity with flexible location options in Hungary, Serbia, UK, Spain, Romania, Slovakia, or Poland.

At Precision for Medicine, we believe in advancing personalized medicine to develop more effective treatments tailored to individual patients. Our mission is to accelerate the development of innovative therapies by developing biomarker-based assays to identify suitable patients and managing all aspects of clinical trials from strategy to execution.

The Patient Data Specialist should possess a strong knowledge of medical and oncology standards relevant to clinical trials, preferably with expertise in hematologic malignancies, to perform scientific review of clinical data in various formats. A medical degree or related qualification (RN, OCN, RPH, PharmD, etc.) with knowledge of hematologic malignancies is preferred.

Essential functions include but are not limited to:

• Reviewing subject data for accuracy according to protocol and oncology standards to ensure data quality and consistency.
• Building and maintaining collaborative relationships within and outside the project team, promoting high-quality standards.
• Supporting cross-functional communication regarding data capture and review trends.
• Contributing to project documentation, including specifications and review guidelines.
• Supporting data output development and user acceptance testing.
• Utilizing various EDC systems and data visualization tools.
• Providing scientific and clinical expertise to project teams.
• Monitoring data quality issues, escalating as necessary, and recommending corrective actions.
• Participating in UAT of programming outputs and reviewing trial protocols from a scientific perspective.
• Assisting in the development of data management strategies and study-specific monitoring tools.
• Reviewing clinical trial data sources for consistency, integrity, and accuracy.
• Communicating findings effectively to the team and management, and providing training as needed.
• Establishing task tracking metrics and providing project updates.
• Ensuring proper documentation and version control of trial-related documents.
• Performing other duties as assigned.

Minimum qualifications:

• Bachelor’s degree or equivalent in science or healthcare with proficiency in medical terminology.

Other requirements:

• Experience in oncology clinical trials, hematologic malignancies preferred.
• At least two years in clinical operations, data management, or related roles in CRO or pharmaceutical industry, or relevant experience as a Study Coordinator, Research Nurse, etc.
• Knowledge of oncology standards, clinical trial methodologies, and experience with EDC systems.
• Understanding of FDA and ICH/GCP regulations.

Highly preferred:

• Medical degree or relevant healthcare qualification.
• Knowledge of hematologic malignancies.

Core competencies and skills:

• Ability to work remotely with minimal supervision, applying oncology knowledge to data review.
• Strong understanding of oncology standards and clinical trial methodologies.
• Continuous learner with adaptability and professionalism.
• Excellent problem-solving, decision-making, and interpersonal skills.
• Proficiency in English, IT tools, and data visualization.
• Willingness to travel up to 25% domestically and internationally.

Join us in revolutionizing cancer treatment through precision medicine, leveraging biomarkers and advanced technological platforms to deliver impactful insights and optimize oncology development.