Senior Manager – Data Management

This is a fully remote position, open to applicants in United States, +2 more locations.

📋 Description

• A degree in a scientific field is required.

• A qualification at the degree level is necessary.

• Demonstrated experience as a Clinical Data Manager within a Pharmaceutical, CRO, or Biotechnology organization is essential.

• A minimum of 5 years of pertinent professional experience in an industry-sponsored clinical trials setting is required.

• Experience in overseeing and managing external data management vendors is preferred.

• Proficiency in Data Management and Project Management is needed.

• Capability to manage complex projects effectively.

• Experience in early-stage oncology clinical development is an asset.

• Understanding of cross-functional roles and responsibilities is important.

• Strong problem-solving and judgment abilities are necessary.

• Excellent oral and written communication skills in English are required.

• Advanced knowledge and application of industry standards and best practices in clinical data management are essential.

• Familiarity with relevant country regulations and standards, including US FDA, ISO, ICH, CDISC, ADaM, and SAS is a must.

• Knowledge in Haematological-Oncology, Autoimmune, or Neuroscience is advantageous; understanding of cell and gene therapy is a plus.

• Previous experience in data management roles in both CRO and sponsor environments is preferred.

⛳️ Requirements

• Possession of a degree in a scientific discipline.

• Degree-level qualification is mandatory.

• Proven track record as a Clinical Data Manager in a Pharmaceutical, CRO, or Biotechnology setting.

• At least 5 years of relevant experience in industry-sponsored clinical trials is essential.

• Experience in the oversight and management of external data management vendors.

• Strong Data Management and Project Management skills.

• Ability to manage complex projects effectively.

• Experience in early oncology clinical development.

• Knowledge of cross-functional roles and responsibilities.

• Strong problem-solving and judgment skills.

• Proficient in oral and written English communication.

• Advanced understanding and application of industry standards and best practices in clinical data management.

• Knowledge of relevant country regulations and standards, including US FDA, ISO, ICH, CDISC, ADaM, and SAS.

• Familiarity with Haematological-Oncology, Autoimmune, or Neuroscience; understanding of cell and gene therapy is an added advantage.

• Preferred experience in both CRO and sponsor data management roles.

🏝️ Benefits

• A flexible, diverse, and dynamic working environment.

• Reasonable accommodations provided during the recruitment process.

• An inclusive and equitable workplace.

• Equal opportunity employment.