We are delighted to be growing our Clinical Data Management Team. We are looking for a proactive and resourceful Clinical Data Manager on a Part-Time basis (circa 20 hours per week) to lead and oversee data management activities for a variety of different clinical development programs. This role is important in ensuring the integrity, quality and timeliness of clinical trial data while maintaining compliance with industry regulations.

The Clinical Data Manager will act as a key liaison between customers, vendors, clinical teams, and cross-functional stakeholders to ensure seamless collaboration and data accuracy.

We are looking for candidates with strong clinical data management skills and great client management skills. 

Key Responsibilities 

• Data Management Study Leadership: Oversee all clinical data management activities, including data collection, validation, cleaning, medical coding and reconciliation processes. 

• Vendor Management: Manage external data management vendors, ensuring deliverables meet quality, regulatory, and timeline expectations. 

• Data Management set-up: Oversee and contribute to the design, development, and review of Case Report Forms, Data Management Plans and other study set up activities e.g. IxRS, ePRO, RBQM processes. 

• Data Validation & Quality Control: Oversee and contribute to the creation and execution of data validation activities to ensure data consistency, accuracy, and completeness, including specifications, EDC checks, data listings and other data review tools to ensure data integrity. 

• Issue Resolution & Support: Troubleshoot data-related issues and provide hands-on support to internal and external stakeholders. 

• Cross-Functional Collaboration: Work closely with clinical operations, biostatistics, regulatory, and programming teams to align data management activities with overall study objectives. 

• Regulatory Compliance: Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements (FDA, EMA). 

• Study Review & Reporting: Participate in data review meetings, contribute to database lock, and support clinical study report preparation. 

• Industry Best Practices: Stay up to date with emerging trends and best practices in clinical data management. 

Skills and Experience Required 

• Bachelor's degree in Life Sciences, Biotechnology, or a related field. 

• Proven experience leading studies in clinical data management within a biotech, pharmaceutical, or CRO environment. 

• Hands-on expertise with a variety of clinical data management systems. 

• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and global clinical trial regulations. 

• Excellent logical, analytical and problem-solving skills with a creative and curious approach to help drive innovation. 

• Experience overseeing data management vendors and ensuring compliance with study timelines and quality expectations. 

• Good customer focus, able to prioritise the needs and satisfaction of our customers and address and resolve conflicts constructively, respectfully and with resilience. 

• Ability to work both independently and collaboratively in a fast-paced, cross-functional environment, and to hold yourself and others to account for appropriate ethical behaviour and inclusivity. 

• Dependable and a commitment to maintaining high data quality standards through a conscientious approach. 

• Strong communication and interpersonal skills for effective collaboration across teams. 

This role is ideal for an experienced clinical data professional who thrives in a collaborative environment and is passionate about advancing clinical research through high-quality data management practices. 

*Note that this initially a part-time role, however, in time there may be the opportunity to increase the number of hours worked, should the individual want to. 

#ACDM2025 #ACDM #clinicaldatamanager #clinicaltrials