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Senior Medical Director, Oncology (Home-Based) – IQVIA Biotech (R1064788)


This is a Contract position in Morrisville, NC posted June 17, 2019.

Job DescriptionJoin us on our exciting journey IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.

Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.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 Novella 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 JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:Functions as project team memberProvides 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 reportingEnsures medical activities run according to GCP and operate with highest efficiencyEstablishes and maintains a network of medical/scientific consultants, etc.Supervises and manages Medical Director activitiesClinical Activities:Interacts with clients regarding drug development programs, study design and protocolReviews 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 areasAssists 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 presentationsPresents protocol and/or safety reporting information at investigator meetingsDevelops project medical monitoring plans as requestedProvides 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 follow-up 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 dataIn 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 requestedData Activities:Provides medical review of eCRFs for clinical accuracyProvides medical review of data analysis planReviews safety fields at case freeze for reconciliation (if needed)Works with data group to reconcile SAE events as neededReviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trendsReviews data tables, listings, and figuresReviews and/or writes portions of final clinical study reportDSMB/Adjudication Committee Activities: May assist sponsor in choosing committee membersMay serve as a non-voting member to convene and organize proceedingsMay develop operating guidelines in conjunction with committee members and submits these to sponsor for reviewMay determine data flow with sponsor to ensure reporting accuracyCan ensure DSMB feedback is given to sites for IRBs All DSMB activities are usually managed by the Novella Oversight Management Group and not the Novella medical monitorBusiness Development ActivitiesWork with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal developmentSupports business development activities with proposal development and sales presentationsParticipates in feasibility discussions relating to specific project proposalsSpecial 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 activitiesParticipate in a variety of team quality improvement efforts as necessaryPerform other related duties as assigned or requested by the Chief Medical OfficerKNOWLEDGE, SKILLS, AND ABILITIES:Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensusOutstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environmentAbility to organize and work efficiently on several projects, each with specific requirements and/or shifting prioritiesExcellent oral and written communications skills as well as interpersonal skills are essentialCRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:Ability to travel domestically and internationally as requiredVery limited physical effort required to perform normal job dutiesMINIMUM RECRUITMENT STANDARDS:Current or prior license to practice medicine; board certification/eligibility idealMinimum 3-5 years of biopharmaceutical industry experience or academic experience in clinical research and drug developmentWe know that meaningful results require not only the right approach but also the right people.

Regardless of your role, we invite you to reimagine healthcare with us.

You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there We invite you to join IQVIA™IQVIA is an EEO Employer
– Minorities/Females/Protected Veterans/DisabledIQVIA, Inc.

provides reasonable accommodations for applicants with disabilities.

Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at to arrange for such an accommodation.Job ID: R1064788 Employee Type:Full-TimeLocation:Morrisville, NCDate Posted:6/11/2019Job ID:R1064788