Senior Data Management Lead

Metronomia Clinical Research; Bloemfontein; Hybrid; GBP 50,000 - 70,000; Full time

Benefits offered by this job

Family-friendly policies

Attractive remuneration

Extensive company social benefits

Opportunities for internal and external training

Job summary

Metronomia Clinical Research is seeking a Project Manager in Clinical Data Management, offering hybrid work options from the UK or full remote. In this role, you will lead study projects, conduct training, and ensure compliance with clinical data management processes.

You should have 3-5 years of experience in the pharmaceutical industry, with expertise in GxP regulations. The company provides a supportive work environment with attractive remuneration, emphasizing appreciation and flexibility for employees.

Qualifications

• At least 3 - 5 years of professional experience in Clinical Data Management.
• Sound knowledge of GxP-regulated clinical research and clinical data management processes.

Responsibilities

• Lead study projects in Clinical Data Management.
• Represent Metronomia in project meetings with customers.
• Support clinical data management including eCRF/ePRO setup and validation.
• Conduct trainings for study teams in Clinical Data Management.
• Support development of Clinical Data Management SOPs.

Skills

Clinical Data Management

GxP-regulated clinical research

CDISC standards

Team collaboration

Communication skills

Education

Relevant training or degree in Clinical Data Management

Job description

(Hybrid based in Bloemfontein, South Africa or Remote located in UK)

Your Tasks

• You will lead study projects in the area of Clinical Data Management or represent and coordinate Metronomia project teams as project manager.
• You represent Metronomia in project meetings with customers and study teams and, if desired, in other customer interactions (e.g. bid defense meetings).
• You are actively involved in the clinical data management of clinical and non-interventional studies. This includes tasks in eCRF/ePRO setup and validation, DMP development, data review & cleaning and import of external data.
• You design and conduct trainings for internal and external study teams in the area of Clinical Data Management.
• You actively support the further development of the Clinical Data Management SOPs.

Your Profile

• You have relevant training or a degree and at least 3 - 5 years of professional experience in Clinical Data Management in the pharmaceutical industry or a CRO.
• You have a sound knowledge of GxP-regulated clinical research, clinical data management processes and CDISC standards.
• You are a team player with high social competence and very good communication skills.

Our offer for you

• Appreciation and family-friendliness! We see and respect you as a person and support your professional compatibility with flexible working models.
• Excellence is worth it! We offer attractive remuneration and extensive company social benefits!
• Flat hierarchy! Our entire team meets at eye level at all times! In this way, we create a special working atmosphere for our highly motivated and qualified team!
• Challenging tasks! There is a detailed introduction to the area of responsibility and regular opportunities for internal and external training!