Clinical Data Management Associate II

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Evaluate project documentation and requirements for new studies while anticipating impacts on Data Management (DM) standards and processes.

• Collaborate with cross-functional project teams to remain updated on changes that affect data collection, cleaning, and transfers.

• Assist in study implementation and data collection activities in accordance with project requirements.

• Define, execute, and review edit checks; identify and rectify data discrepancies.

• Maintain organized, complete, and up-to-date study documentation.

• Create and/or review study Transmittal Forms, ensuring compliance with established standards.

• Keep the supervisor updated on project status, risks, and milestones.

• Examine clinical data to detect errors and inconsistencies.

• Develop specifications for study data, including data transfer specifications, system configuration specifications, and data validation rules.

• Collaborate with project teams to address data issues and track outstanding actions to resolution.

• Prepare and validate ad hoc data listings as necessary.

• Ensure that system bugs and enhancement needs are reported to the appropriate Product Manager and that any interim programming solutions receive approval.

• Adhere to departmental processes, standards, and relevant Standard Operating Procedures (SOPs).

• Participate in the review and updating of SOPs pertaining to Data Management.

• Work with internal colleagues to resolve issues and support team objectives.

• Contribute ideas to enhance processes and add value to the organization.

• Support team success by assisting others when necessary.

• Engage in relevant company-sponsored training to maintain technical and industry knowledge.

• Perform other assigned duties.

⛳️ Requirements

• Bachelor’s degree in Computer Science, Life Sciences, or a related field is preferred, or equivalent relevant experience.

• Approximately one year of experience in a similar role within the pharmaceutical, biotechnology, or CRO industry.

• Working knowledge of relational database organization and principles of data validation.

• Experience with office productivity tools such as Microsoft Word, Excel, and Access is preferred.

• Familiarity with clinical trial terminology.

• Proven problem-solving skills.

• Ability to work independently while effectively contributing within a team environment.

• Strong attention to detail and excellent organizational skills.

• Effective interpersonal and communication skills, both written and verbal.

• Professional demeanor with a positive approach and the capacity to adapt to changing priorities.

🏝️ Benefits

• Competitive compensation and benefits.

• Opportunity to work remotely within the United Kingdom.

• A collaborative, global environment that supports professional growth and development.