Senior Medical Director, Hematology/Oncology
Senior Medical Director, Hematology/Oncology
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Job Description
The medical department consists of a Chief Medical Officer Medical Directors medical writers and safety associates. The Senior Medical Director provides medical and scientific support to clinical research programs study teams and investigators. The Senior Medical Director also provides review advice and leadership for potentially or actually awarded clinical research programs.
The Senior 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 Senior 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.
Essential Functions
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 nonserious adverse event evaluation and reporting
Ensures medical activities run according to GCP and operate with highest efficiency
Establishes and maintains a network of medical/scientific consultants etc.
Supervises and manages Medical Director activities
Clinical Activities:
Interacts with clients regarding drug development programs study design and protocol
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 team approach to develop statistical and data management sections of the protocol. Reviews the final protocol for clinical safety and efficacy variables.
Provides project team training on protocol and/or therapeutic areas
Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
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
Presents protocol and/or safety reporting information at investigator meetings
Develops project medical monitoring plans as requested
Provides on call coverage for protocol queries and site support. Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
Safety Monitoring and SAE Reporting Activities:
Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study
Provides medical review of SAE reporting writes and/or reviews SAE narratives and works with the Safety Management Department to track SAEs and followup on outstanding safety queries interacts with sponsor and discusses safety issues with site as needed
Reviews IND/SUSAR Safety Reports (per sponsor preference) updates to Investigator Brochures and annual IND reports with sponsor data
In consultation with the sponsor follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind)
Interact with appropriate FDA officials concerning safety and other study related issues as requested
Data Activities:
Provides medical review of eCRFs for clinical accuracy
Provides medical review of data analysis plan
Reviews safety fields at case freeze for reconciliation (if needed)
Works with data group to reconcile SAE events as needed
Reviews medical coding of adverse events laboratory data and concomitant medications for accuracy coherence consistency and trends
Reviews data tables listings and figures
Reviews and/or writes portions of final clinical study report
DSMB/Adjudication Committee Activities:
May assist sponsor in choosing committee members
May serve as a nonvoting member to convene and organize proceedings
May develop operating guidelines in conjunction with committee members and submits these to sponsor for review
May determine data flow with sponsor to ensure reporting accuracy
Can ensure DSMB feedback is given to sites for IRBs
Business Development Activities
Work with Business Development to actively solicit new business including assistance with marketing presentations and proposal development
Supports business development activities with proposal development and sales presentations
Participates in feasibility discussions relating to specific project proposals
Special Projects:
Obtain 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 all Medical Director activities
Participate in a variety of team quality improvement efforts as necessary
Perform other related duties as assigned or requested by the Chief Medical Officer
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. Req
Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Typically requires 57 years of relevant experience in the requested medical specialty area in clinical medicine as licensed physician. A boardcertification for the required therapeutic area is an advantage. Expected is 5 years experience in clinical research as study physician/investigator or in the Pharma CRO or Biotech industry
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
Current or prior license to practice medicine; board certification/eligibility ideal
Board Certified / Board Eligible: Oncology/ Hematology
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $223900.00 $415900.00. The actual base pay offered may vary based on a number of factors including jobrelated qualifications such as knowledge skills education and experience; location; and/or schedule (full or parttime). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.
Required Experience:
Director
Employment Type
Full-Time
