Clinical Research Manager (Future Opportunity)
Posted 2 days ago by Novartis
Negotiable
Undetermined
Undetermined
London, England, United Kingdom
Summary: This temporary contractor role at Novartis involves contributing to operational and clinical trial deliverables, ensuring compliance with quality standards and timelines. The position requires oversight of study start-up activities and adherence to Novartis policies and external regulations. The role emphasizes proactive operational planning and high-quality contributions to clinical documentation. Candidates will work collaboratively within a global medicines company to enhance their skills and experiences in clinical operations.
Key Responsibilities:
- Contributes to all operational/clinical trial deliverables according to timelines, budget, and quality standards.
- Conducts study start-up activities including protocol and CRF development.
- Ensures proper handling of study conduct and close-out activities.
- Responsible for education, implementation, and compliance with clinical operations standards.
- Reports technical complaints/adverse events related to Novartis products within 24 hours.
- Performs clinical data review and insights consistently and accurately.
- Contributes to study/program level and submission documents.
- Supports management in team competency building and best practice sharing.
Key Skills:
- Financial Management
- Operations Management and Execution
- Project Management
- Budget Management
- Clinical Research
- Clinical Trial Protocol
- Coaching
- Data Analysis
- Data Integrity
- Learning Design
- Lifesciences
- Risk Monitoring
- Trends Analysis
- English language proficiency
Salary (Rate): undetermined
City: London
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
This is a temporary contractor opportunity at Novartis Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life! Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit. Ready to work with/through Magnit at Novartis? Please read on…
Major accountabilities:
- Contributes to all operational/clinical trial deliverables that are in scope of the specific JD, according to timelines, budget, operational procedures, quality /compliance and performance standards.
- Conduct/Contribute to study start-up activities such as overseeing protocol development, CRF development, Informed Consent Form development
- Ensuring proper handling of all study conduct and close out activities including but not limited to site close out, final drug accountability and audit readiness of Trial Master File documentation (if in scope of the specific JD).
- Responsible for education, implementation and compliance to standards (SOPs) and best practices for clinical operations/clinical data review activities within assigned clinical trial(s) and within clinical program(s), including sharing lessons learned.
- Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
Key performance indicators:
- Timely, efficient and quality execution of assigned trials and trial related activities within budget, and in compliance with quality standards.
- Proactive operational planning with effective contingency and risk mitigation plans.
- Adherence to Novartis policy and guidelines and external regulations -Performing clinical data review and insights consistently and accurately which meets the Novartis quality standards, timelines, and is inspection ready.
- High quality contributions to study/ program level and/or submission documents (e.g. IDP, protocol, ICF, clinical sections of CTA).
- Strong leadership skills to be able to support management in team competency building, lead/contribute to local/global initiatives and best practice sharing across programs and/or departments -Clearly demonstrates Novartis Values and Behaviors (i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity.
Minimum Requirements:
- Work experience: Financial Management. Collaborating across boundaries. Operations Management and Execution. Project Management.
- Skills: Budget Management. Clinical Research. Clinical Trial Protocol. Clinical Trials. Coaching. Data Analysis. Data Integrity. Learning Design. Lifesciences. Risk Monitoring. Trends Analysis.
- Languages: English.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accommodation: If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.