Senior Clinical Data Manager

About Convatec

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com

About the role

The Clinical Data Manager (CDM) is accountable for clinical data management activities in support of the clinical pipeline. This may include, but is not limited to, execution and ownership of the CDM operating model, oversight of internal staff, and cross-functional leadership for the delivery of high quality and reliable clinical data to enable internal decision making, regulatory approval, and market acceptance. The CDM interacts with senior level management, collaboration partners and provides cross functional strategic direction and identify risks and opportunities as well as innovative approaches to clinical data management. The CDM is critical to the success of our clinical trials and the integrity of data that supports regulatory submissions and decision-making.

Key Responsibilities:

• Establishing and driving global data management and data analytics strategy related to technologies and

• processes to increase efficiency, innovation and data quality.

• Provide data collection, cleaning, and integration expertise in support of global development projects

• including all disease areas and business units; ensure functional strategy supports the portfolio priorities

• while also remaining close to the business and portfolio.

• Building efficient and compliant processes to support regulatory inspections.

• Ability to effectively manage the anticipated growth in the global product

Skills & Experience:

• Key competencies and characteristics needed to help build our diverse, inclusive culture and to be

• successful in the role. Examples include:

• Overseeing the collection, validation, processing and analyzing of clinical trial data.

• Developing and implementing data management and data analytic procedures for clinical trials.

• Supporting and facilitating the review of medical coding for validity and completeness.

• Ensuring compliance with applicable regulations, protocols and standard operating procedures.

• Maintain the highest data quality standards throughout the data lifecycle, from data collection to

• database lock.

• Stay updated on industry best practices, technological advancements and regulatory requirements related to clinical data management and data analytics.

• Develop and maintain data management documentation, including clinical study protocols, statistical analysis plans, case report forms and data management plans.

Qualifications/Education:

• Bachelor’s degree in a scientific or healthcare-related field or a computer science degree or equivalent

• professional certification.

• Minimum of 5 years of experience in clinical data management or a similar role in the medical device or

• clinical research industry.

• Strong understanding of clinical trial processes, data management principles and regulatory guidelines.

• Proficiency in electronic data capture (EDC) systems and clinical data management software.

• Familiarity with relevant regulations and guidelines, like GCP and CDISC standards.

• Knowledge of industry-standard data analysis and reporting software, such as SAS, SQL and/or Oracle Clinical.

• Excellent attention to detail with problem-solving and analytical skills.

• Strong organizational and time management abilities.

What You’ll Get:

• Impactful Work: Play a key role in shaping the future of healthcare by ensuring the integrity of clinical data that supports global regulatory submissions and product innovation.

• Global Collaboration: Work alongside talented professionals across clinical, regulatory, and technical teams in a dynamic, international environment.

• Career Growth: Access to continuous learning, development programs, and opportunities to advance within a growing organization.

• Innovation-Driven Culture: Be part of a company that values new ideas, cutting-edge technologies, and data-driven decision-making.

• Competitive Compensation: Attractive salary package, performance-based bonuses, and comprehensive benefits.

• Work-Life Balance: Flexible working arrangements and a supportive culture that values your well-being.

• Inclusive Environment: Join a diverse and inclusive team where your voice matters and your contributions are recognized.

Ready to join us?

At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life.

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Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

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