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Medical Director- Oncology/Hematology (Home-Based), Warsaw

Client: IQVIA

Location: Warsaw, Poland

Job Category: Other

EU work permit required: Yes

Job Reference: 7e405662124c

Job Views: 21

Posted: 23.01.2025

Expiry Date: 09.03.2025

Job Description:

Job Overview

The medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scientific support to clinical research programs, study teams, and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.

The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:

Essential Functions

1. Functions as project team member.
2. Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation and reporting.
3. Ensures medical activities run according to GCP and operate with highest efficiency.
4. Establishes and maintains a network of medical/scientific consultants, etc.
5. Supervises and manages Medical Director activities.
6. Interacts with clients regarding drug development programs, study design and protocol.
7. Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
8. Provides project team training on protocol and/or therapeutic areas.
9. Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation.
10. Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators and site staff and/or participation in teleconference and WebEx presentations.
11. Presents protocol and/or safety reporting information at investigator meetings.
12. Develops project medical monitoring plans as requested.
13. Provides on call coverage for protocol queries and site support.

Safety Monitoring and SAE Reporting Activities:

1. Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
2. Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs.
3. Reviews IND/SUSAR Safety Reports, updates to Investigator Brochures, and annual IND reports with sponsor data.
4. Provides medical review of eCRFs for clinical accuracy.

Qualifications

Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.

10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.

3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.

Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.

Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.

Excellent oral and written communications skills as well as interpersonal skills are essential.

Oncology; Hematology;

Current or prior license to practice medicine; board certification/eligibility ideal (Preference).

Board Certified / Board Eligible: Oncology/ Hematology (Required).

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

Warszawa - Oferty pracy w okolicznych lokalizacjach