Clinical Data Management Development Specialist, Remote, Europe Lisboa

Clinical Data Management Development Specialist, Remote, Europe
Lisboa
Lisboa, Portugal

Clinical Data Management Development Specialist, Remote, Europe, Lisbon

Client:

IQVIA

Location:

Lisbon, Portugal

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

ef7a8a305472

Job Views:

46

Posted:

23. 01. 2025

Expiry Date:

09. 03. 2025

Job Description:

Job Description

Summary

1. Collaborate with Subject Matter Experts and the Real World Evidence Data Management Team to develop and maintain Training Plan requirements and roles.
2. Facilitate quarterly or annual training plan reviews.
3. Develop training slides and material independently or with Subject Matter Experts.
4. Plan, coordinate and communicate the training schedule for the Real World Evidence Data Management department.
5. Perform training courses as needed and agreed with other stakeholders.
6. Provide oversight of training delivered by other stakeholders.
7. Monitor effectiveness and timeliness of training.
8. Set up and maintain folder on Data Management Share
   Point site.
9. Update/archive training items in alignment with Training Plan updates.
10. Plan and support development of Compliance Reports.
11. Provide review and/or oversight of staff onboarding training compliance.
12. Provide review and/or oversight of monthly/quarterly training compliance data.
13. Collaborate with Managers to ensure adherence to training compliance targets.
14. Participate, support or lead global initiatives to continuously improve training processes or compliance across Real World Evidence Data Management.
15. Provide input on Data Management process improvements.
16. Provide input on the development and implementation of a new technology or tool.
17. Participate in focus teams, and global or local best practice teams as relevant.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

1. Sound working knowledge of clinical data management procedures, ICH-GCP, applicable regulatory requirements, medical terminology and quality management processes.
2. Knowledge of Drug Development processes.
3. Knowledge of CRO or Pharmaceutical Industry operations.
4. Sound knowledge of current training practices.
5. Good organizational, interpersonal and communication skills.
6. Good judgement and
   - making skills.
7. Strong influencing and negotiation skills.
8. Strong computer skills including Microsoft Office and Data Management applications including EDC (Medidata Rave).
9. Demonstrated ability to work in a matrix environment.
10. Excellent
    - solving skills.
11. Ability to travel within the region/country.
12. Ability to lead and motivate a training team.
13. Ability to establish and maintain effective working relationships with
    - workers, managers and clients/customers.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at.

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