Sr./Medical Director, Oncology or Hematology (Home-Based) - IQVIA Biotech (Open)
IQVIA
Buenos Aires, Argentina
hace 3 días

IQVIA Biotech is seeking an Oncology and / or Hematology, Board Certified or Eligible physician for the position of Senior / Medical Director.

  • The Medical Director is the assigned Medical Monitor providing medical oversight as the first line of support for clinical trials;
  • current clinical research experience required. Excellent Home-Based opportunity for individuals located in the United States, Canada, Argentina, Brazil and Mexico .

    IQVIA Biotech , a division of IQVIA, delivers flexible, tailored, clinical and commercial solutions designed for biotech and biopharma companies.

    From planning, through trial design and delivery, and commercialization, IQVIA Biotech brings simplified operating procedures, specialized, therapeutically-aligned teams, and advanced data science to provide a more agile way for our customers to reach their drug development and commercialization milestones.

    POSITION TITLE : Senior / Medical Director

    REPORTS TO : Vice President, Medical or Designee

    BASIC FUNCTIONS :

  • The medical department consists of the Vice President, Medical; Senior Director, Medical Operations; Senior Directors, Medical;
  • Senior Medical Directors and Medical Directors; Medical Data Review Directors; Medical Safety and Data Reviewers; Medical Operation Bidders;
  • and Medical Monitor Operations Specialists.

    The Senior Medical Director provides medical and scientific support to clinical research programs, study teams, and investigators.

    The Senior Medical Director also provides medical leadership, review, and advice for potentially or actually awarded clinical research programs.

    He / she also may serve as a Medical Mentor to junior staff members. The Senior Medical Director may serve as lead on special projects or assignments for the Medical Department, as requested by the VP, Medical or designee.

    The Senior Medical Director role is a team member participant role and functions in a matrix and reports to project teams much like other members of project teams.

    The primary role of Senior Medical Director is to serve as Medical Monitor for studies conducted by IQVIA Biotech on behalf of sponsor companies.

    In the role of Medical Monitor, the Senior Medical Director provides medical oversight as the first line of support for clinical trials to which he / she is assigned as Medical Monitor.

    The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as a medical resource to support the project team.

    The Medical Monitor is customarily available 24 / 7 to answer questions from site coordinators and investigators and study team members on protocol inclusion / exclusion criteria, protocol clarifications, and compliance issues.

    Major duties of the Medical Director are outlined below :

    ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES :

    Medical Monitoring :

    Clinical Activities :

  • Per sponsor request, reviews and provides input for protocol development; interacts with key thought leaders and / or sponsor representatives to develop inclusion / exclusion criteria and study endpoints;
  • interacts in a team approach to develop statistical and data management sections of the protocol; reviews the final protocol for clinical, safety and efficacy variables

    Functions as project team member

    Provides project team with training on therapeutic indication and / or treatment modality

    May provide study team with assistance in developing criteria for investigator site selection and networking for potential investigators for study participation, and aid in review and final selection

    Participates in subject recruitment and retention activities which may include per sponsor request individual calls to key opinion leaders, investigators and site staff, and participation in teleconference and virtual presentations

    Per sponsor request, presents protocol and / or safety reporting information at investigator meetings

    Develops project medical monitoring plan

    Provides first line contact for investigators and monitors regarding study related medical / safety issues and resolution of study protocol and patient eligibility issues

    Provides medical input into the development of study protocols, training materials, informed consent, Investigator Drug Brochures, analysis plan designs, clinical study reports, regulatory approval submissions

    Provides on call coverage for protocol queries and site support

    Safety Monitoring and SAE Reporting Activities :

    Works with the IQVIA Biotech or vendor Safety Management Department to provide medical review and case assessment of SAEs / UADEs including review and edits of SAE narratives and safety queries, follow-up on outstanding safety queries, and interacting with sponsors and investigative sites to discuss safety issues as needed

    Per sponsor request, reviews IND / SUSAR Safety Reports, updates to Investigator Brochures, and annual IND reports with sponsor data

    In consultation with the sponsor, follows procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind)

    Interacts with regulatory officials concerning safety and other study related issues, as requested

    Data Activities :

    Provides medical review of eCRFs and edit check specifications for clinical accuracy

    When indicated, provides Medical Data Review Plan as appendix to the Medical Monitoring Plan

    Performs medical review of coded terms (e.g. adverse events, concomitant medications and medical history) for medical accuracy and consistency

    Provides individual and aggregate review of clinical data as requested and specified in the Medical Data Review appendix

    Reviews laboratory data as requested by sponsor and as specified in the MMP or Medical Data Review Appendix

    Reviews data tables, listings, and figures as requested by sponsor

    Reviews and / or writes portions of final clinical study report as requested by sponsor

    Business Development Activities :

    Works with Business Development to actively solicit new business for IQVIA Biotech, including assistance with marketing presentations and proposal development

    Interacts with clients regarding drug development programs, study design and protocol development

    Reviews and provides medical and scientific input to new business proposals

    Participates in feasibility discussions relating to specific project proposals

    Supports business development activities with proposal development and sales presentations

    Special Projects :

    Obtains literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.

    Assists with drafting of standard operating procedures and working practices regarding Medical Director activities

    Participates in a variety of team quality improvement efforts as necessary

    Performs other related duties as assigned or requested by the Vice President, Medical or designee

    KNOWLEDGE, SKILLS, AND ABILITIES :

    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

    Ability to organize and work efficiently on several projects, each with specific requirements and / or shifting priorities

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

    CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA :

    Ability to travel domestically and internationally as required

    Very limited physical effort required to perform normal job duties

    MINIMUM RECRUITMENT STANDARDS :

    Current or prior license to practice medicine; board certification / eligibility ideal

    10 years’ experience relevant to drug development and clinical research, including 3-5 years of biopharmaceutical industry, academic, and / or clinical practice experience

    Oncology and / or Hematology Board Certification or Eligibility required

    CLASSIFICATION :

    This position is classified as exempt under the Fair Labor Standards Act; employees are not eligible for overtime compensation.

    LI-AL3

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