Manager, Clinical Science Analytics & Insights

Precision Medicine Group; Almería; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in clinical science analytics is seeking a Manager to enhance team performance and ensure high-quality deliverables. This role involves managing operations, developing staff, and supporting business initiatives. The position offers the opportunity to work remotely across several countries, making it ideal for experienced professionals in clinical research.

Formación

• At least 8 years of clinical research experience.
• 2-3 years of direct supervisory experience managing CRAs.

Responsabilidades

• Managing daily operations and departmental initiatives.
• Overseeing onboarding and functional training for new team members.
• Supporting project and financial management tasks.

Conocimientos

Communication

Interpersonal Skills

Problem-Solving

Educación

Bachelor’s degree in a science or health-related field

Herramientas

Microsoft Office Suite

Electronic Data Capture Systems

Data Visualization Software

Descripción del empleo

Manager, Clinical Science Analytics & Insights

2 days ago Be among the first 25 applicants

Precision for Medicine is seeking a Manager to join our Clinical Science Analytics & Insights team. This role can be fully remote in the UK, Spain, Poland, Slovakia, Romania, Hungary, or Serbia.

Position Summary

The Manager, Clinical Science Analytics & Insights (CSAI) is responsible for managing and developing CSAI personnel, serving as a departmental SME to support initiatives, business development, best practices, and training to enhance quality and productivity. The role requires leading, managing, and motivating a team of CSAI staff or consultants, ensuring proper resource allocation and tools for success. Additionally, the manager will support career development to reduce turnover and maintain high employee satisfaction.

Essential Functions include but are not limited to:

1. Managing daily operations of direct reports and departmental initiatives, ensuring project deliverables are met.
2. Developing direct reports through goal setting, performance reviews, and mentoring.
3. Overseeing onboarding and functional training for new team members.
4. Communicating strategic direction and supporting career development, training, and mentoring.
5. Ensuring compliance with policies, SOPs, guidelines, and GCPs.
6. Retaining high-quality CSAI staff.
7. Participating in the CSAI management team, supporting departmental KPIs and objectives.
8. Supporting project and financial management tasks, such as invoicing.
9. Providing departmental expertise and fostering cross-functional communication.
10. Contributing to policy and process development for CSAI.
11. Preparing reports and supporting risk management initiatives.
12. Addressing complex challenges related to people and processes.
13. Ensuring systems and processes produce quality work efficiently.
14. Supporting resource allocation and forecasting.
15. Participating in business development, including proposals and bid defenses.
16. Engaging in departmental, vendor, and client meetings.
17. Supporting process improvements and operational solutions.
18. Collaborating on training initiatives and SOP development.
19. Consulting with project teams on project issues.
20. Performing other duties as assigned.

Qualifications

Minimum Required:

• Bachelor’s degree or equivalent in a science or health-related field with proficiency in medical terminology.
• At least 8 years of clinical research experience or equivalent competencies.
• Strong experience in oncological clinical trials, including on-site monitoring and/or data review.
• 2-3 years of direct supervisory experience managing CRAs, including developing staff and evaluation processes.

Other Required:

• Experience with electronic data capture systems.
• Proficiency in Microsoft Office Suite.
• Excellent communication and interpersonal skills.
• Professional proficiency in English, both written and oral.
• Willingness to travel domestically and internationally occasionally.

Preferred:

• Medical degree or related qualifications (RN, OCN, RPH, PharmD, etc.).
• Experience with database build and data visualization software (e.g., JReview).
• Knowledge of FDA & ICH-GCP regulations, SOPs, and clinical trial processes.
• Highly organized with problem-solving skills and continuous improvement focus.
• Understanding of clinical trial methodology and protocols.
• Ability to manage multiple priorities and apply financial skills at the project level.
• Excellent presentation and communication skills.

Any data provided will be stored according to our Privacy Policy. For CA applicants, please refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to protected characteristics. For accommodations, contact us directly.

Beware of fraudulent job offers; our organization will only extend offers through verified communication channels.