Manager, Clinical Data Management

We're on a mission to change the future of
clinical research. At Perceptive, we help the
biopharmaceutical industry bring medical
treatments to the market, faster.
Our mission is to change the world
but to do this, we need people like you.

Apart from job satisfaction, we can offer you:

YOURSELF

• Starting at 14 days holiday per year, rising to 22 days with increased service. In addition to public holidays

• Life Events, Service Awards, Company Outings

HEALTH

• Medical plan

• Annual medical check

WEALTH

• Social security and public housing fund

• Supplementary Housing Allowance

• Life assurance

• Critical illness cover

Responsibility

• Leads, mentors and develops a clinical data management team through direct line management.
• Provides training on Data Management procedures.
• Provides training and monitors performance to ensure the team are operating at the highest level to design and deploy clinical databases for multiple clinical imaging studies.
• Manages team workload and prioritization for all assigned staff.
• Acts as resource manager for dedicated therapeutic area.
• Sets clear goals, providing regular feedback and fostering a collaborative team environment.
• Conducts one-on-one meetings.
• Mentors and ensures the team adheres to best practices and industry standards and facilitates positive career growth.

• Creates study Data Management Plans and deployment roadmaps.
• Oversees and participates in the design of study CRFs and databases utilizing eCRF library.
• Provides guidance as clinical database development subject matter expert.
• Monitors study timelines and communicates risk.
• Acts as sponsor portfolio lead representative.
• Oversees multiple concurrent projects.
• Facilitates study team involvement in database development.
• Utilizes metrics to monitor study health.
• Communicates with sponsors and internal leadership regarding study data processes, endpoints, and overall data management process.

• Creates and maintains Standard Operating Procedures.
• Provides guidance on Data Management best practices and regulatory considerations.
• Defines new procedures and solutions for novel therapeutics and study endpoints.

• Carries out any other reasonable duties as requested.

• Excellent demonstrable knowledge of regulatory guidelines and requirements for clinical data management.
• Displays excellent understanding of clinical trial data standards.
• Understanding of clinical trial processes, protocols, and regulatory requirements (e.g., FDA guidelines) related to data management.
• Excellent communication (oral and written) and interpersonal skills, to convey data-related information to technical and non-technical stakeholders (internal and external) including clients and research centres.
• Excellent analytical skills with attention to detail and the ability to identify data discrepancies and trends.
• Ability to manage multiple tasks and prioritize work in a fast-paced and deadline-driven environment, with the ability to raise potential issues with deliverables on time.
• Detail oriented and possess excellent organizational skills.
• Builds and maintains an up-to-date awareness of industry trends, best practices, and emerging technologies in data management for clinical research.
• Ability to work collaboratively within a matrix team environment.
• Ability to effectively motivate and guide team members towards shared goals.
• Natural coach/mentor who leads by example with an approachable demeanour and visible leader skills.
• A self-starter and able to work under own initiative.
• Strong analytical and creative problem-solving skills to identify issues and propose solutions.
• Displays technical project management skills and oversight.
• Ability to manage task creation and tracking via ticketing software.
• Demonstrates meticulous attention to detail, documentation and adherence to study protocols and standard operation procedures (SOPs).

• Accountability
• Adaptability
• Customer focus
• Robust
• Decision Making
• Time Management
• Analytical thinking
• Results orientation
• Conflict Management
• Business Acumen
• Developing direct reports and others

• Significant demonstrable practical work experience in a clinical or technical setting.
• Line management experience.
• Demonstrable experience in team settings to achieve goals.
• Demonstrable experience and proficiency with clinical data management systems.
• Experience working with research support or clinical team.
• Proficiency in Microsoft Office Suite (Word, Excel (macros), PowerPoint) and data visualization tools is preferred.
• Bachelor's Degree in Life Science (Biology, Medical Technology, Research Psychology, Math or Health Science) or equivalent experience in a related field.

• English: Fluent.