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Manager, Clinical Science Analytics & Insights

Precision Medicine Group

Poland (ME)

Remote

USD 80,000 - 120,000

Full time

2 days ago
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Job summary

An established industry player is seeking a dynamic Manager for their Clinical Science Analytics & Insights team. This role offers the opportunity to lead and develop a talented team while enhancing operational efficiency and quality in clinical research. You'll be responsible for managing daily operations, mentoring staff, and ensuring compliance with regulatory guidelines. The position emphasizes growth, communication, and problem-solving, making it perfect for someone passionate about clinical science and team development. Join a forward-thinking company dedicated to improving patient outcomes through innovative research.

Qualifications

  • 8+ years of clinical research experience with strong oncological trial background.
  • 2-3 years of supervisory experience managing clinical research associates.

Responsibilities

  • Manage daily operations and workload of the CSAI team.
  • Support career development and mentoring for staff.

Skills

Clinical Research
Oncological Clinical Trials
Team Management
Communication Skills
Problem-Solving

Education

Bachelor's degree in Science or Health-related field
Medical degree or related qualification

Tools

Electronic Data Capture Systems
Microsoft Office
Data Visualization Software (e.g., JReview)

Job description

Manager, Clinical Science Analytics & Insights

Precision for Medicine is looking for a Manager to join our Clinical Science Analytics & Insights team. The position can be fully remote within the UK, Spain, Poland, Slovakia, Romania, Hungary, or Serbia.

Position Summary:

The Manager, Clinical Science Analytics & Insights (CSAI) is responsible for managing and developing the careers of CSAI personnel, serving as a departmental SME supporting initiatives, business development, best practices, and training to enhance quality and productivity. This role requires leading, managing, and motivating a team of CSAI staff or consultants, ensuring resources are properly allocated and equipped. Additionally, the manager will support career development and employee satisfaction to reduce turnover.

Essential functions include:

  1. Managing daily operations and workload of direct reports and departmental initiatives.
  2. Developing staff through goal setting, performance reviews, and mentoring.
  3. Overseeing onboarding and functional training of new team members.
  4. Communicating strategic goals and supporting career development, training, and mentoring.
  5. Ensuring compliance with policies, SOPs, and regulatory guidelines.
  6. Retaining high-quality CSAI staff.
  7. Participating in management team activities and supporting departmental KPIs.
  8. Supporting project and financial management tasks.
  9. Providing departmental expertise and fostering cross-functional communication.
  10. Developing and updating policies, processes, and reports.
  11. Supporting risk management and addressing complex challenges.
  12. Ensuring systems and processes produce quality work efficiently.
  13. Allocating resources and forecasting workload.
  14. Participating in business development activities, including proposals and bid defenses.
  15. Engaging in departmental, vendor, and client meetings.
  16. Contributing to process improvement initiatives and implementing solutions for operational challenges.
  17. Collaborating on training initiatives and reviewing SOPs and tools.
  18. Consulting on project-related issues as needed.
  19. Performing other duties as assigned.

Qualifications:

  • Bachelor’s degree or equivalent in science or a 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 data review.
  • 2-3 years of direct supervisory experience managing CRAs, including developing staff, performing evaluations, and training.

Other requirements:

  • Experience with electronic data capture systems and Microsoft Office.
  • Excellent communication and interpersonal skills in English.
  • Ability to travel domestically and internationally as needed.

Preferred qualifications:

  • Medical degree or related qualification (RN, OCN, RPH, PharmD, etc.).
  • Experience with database build and data visualization software like JReview.
  • Knowledge of FDA & ICH-GCP regulations and clinical trial processes.
  • Highly organized with problem-solving skills and a focus on continuous improvement.
  • Understanding of clinical trial methodologies and protocols.
  • Financial management skills at the project level.
  • Excellent presentation and communication skills.

#LI-TB1

We comply with privacy policies and are an Equal Opportunity Employer. For accommodations, contact QuestionForHR@precisionmedicinegrp.com.

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