Urwah Admin

IQVIA

<div>Job Overview
 
Under broad guidance, executes and verifies software application tests.
<div>Essential Functions
 
<ul><li>Analyzes business and functional requirements for completeness; derives valid test cases.
</li><li>Carries out procedures to ensure that all information systems products and services meet minimum organization standards and end-user requirements.
</li><li>Defines master test plans to document overall testing strategy for a project.
</li><li>Executes test scripts to test software, documenting validation of test scenarios, defects, and resolution.
</li><li>Analyzes test results; reviews test plans and supporting execution documentation as required.
</li><li>Provides risk assessment throughout test cycles and create lessons learned summary upon completion of project.
</li><li>Reads, analyzes, and interprets project requirement and technical design documents.
</li><li>Writes test plans for application functionality and software systems using a prescribed style and format.
</li><li>Effectively presents information in both written and verbal form to management, customers (internal only), or other technical personnel.
</li></ul></div><div>Qualifications
 
<ul><li>Bachelor's Degree Computer Science, a related field, or equivalent experience
 </li></ul>Req
 
<ul><li>Three (3) years related experience in quality assurance and testing Req
</li></ul></div>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 https://jobs.iqvia.com</div>

Software QA Engineer

<div>Location: Riyadh
 
Function: Growth &amp; Commercial, Sales
 
Reports to: Commercial Manager L.S Saudi Arabia 
 
 
 
Role Summary 
 
IQVIA is seeking a Senior Account Manager, Sales to drive business growth with multinational pharmaceutical clients across KSA. This role covers the full IQVIA portfolio&mdash;Consulting, Analytics, Real-World Evidence (RWE), HEOR, Market Research, Technology Platforms, and Patient Support Programs (PSPs).
 
 
You will act as a trusted commercial partner for senior stakeholders within leading global pharma companies, shaping integrated solutions that accelerate launches, optimize portfolios, and deliver measurable patient impact.
 
 
Key Responsibilities
 
 
Account &amp; Client Leadership 
 
&bull; Manage and grow a portfolio of strategic multinational pharma accounts; serve as the single point of accountability for sales and client satisfaction.
 
&bull; Develop strategic account plans aligned with client objectives and
 
 
IQVIA growth targets 
 
&bull; Build relationships with Country Managers, BU Heads, Market Access Directors, Medical/HEOR Leaders, and Digital/Commercial Directors. 
 
Business Development 
 
&bull; Identify, qualify, and close opportunities across consulting, syndicated data, market research, analytics, and technology solutions.
 
&bull; Lead end-to-end sales cycle: discovery, solution design, proposal development, negotiation, contracting, and handover to delivery teams.
 
&bull; Ensure cross-sell and up-sell of IQVIA offerings, expanding share of wallet across accounts.
 
 
Solution Expertise 
 
&bull; Position IQVIA&rsquo;s broad capabilities, including:
 
o Consulting &amp; Strategy: launch readiness, portfolio optimization, go-to-market, pricing &amp; market access.
 
o RWE &amp; HEOR: evidence generation, burden of illness, outcomes research, payer engagement.
 
o Technology: CRM, omnichannel, patient engagement platforms, advanced analytics.
 
o Market Research &amp; Insights: physician, payer, and patient insights; competitive intelligence.
 
o Patient Support Programs: adherence, education, access facilitation.
 
&bull; Translate client challenges into actionable IQVIA solutions with clear ROI.
 
 
Collaboration &amp; Execution 
 
&bull; Partner with consulting principals, RWE/HEOR specialists, PSP managers, and technology teams to design integrated solutions.
 
&bull; Maintain CRM discipline (pipeline hygiene, forecasting, activity tracking) and deliver accurate monthly/quarterly revenue projections.
 
&bull; Ensure seamless handover and governance of sold projects; monitor delivery satisfaction to drive renewals.
 
 
Qualifications &amp; Experience 
 
&bull; 7&ndash;10 years of commercial experience in healthcare/life sciences, with at least 4&ndash;5 years in front-line sales or account management.
 
&bull; Proven record of quota attainment and account growth with multinational pharma companies.
 
&bull; Strong knowledge of pharma value chain: clinical development, launch, market access, commercial excellence, patient engagement.
 
&bull; Experience selling consulting projects, RWE/HEOR, syndicated data, or technology solutions to pharma clients.
 
&bull; Demonstrated ability to influence senior decision-makers.
 
&bull; Bachelor&rsquo;s degree in Business, Science, or related field required.
 
&bull; English required; Arabic strongly preferred.
 
&bull; Willingness to travel up to 30&ndash;40%.
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 https://jobs.iqvia.com</div>

Senior Account Manager , Sales – Pharma (Life Sciences)

<div>Location: Riyadh
 
Function: Growth &amp; Commercial, Sales
 
Reports to: Commercial Director L.S Saudi Arabia
 
 
Role Summary 
 
IQVIA is seeking a Senior Account Manager, Sales to accelerate growth with consumer health clients (OTC, nutrition, wellness, personal care, FMCG-health, pharmacies, and retail health chains). The role spans IQVIA&rsquo;s full portfolio of life science offerings&mdash;Consulting, Analytics, Technology, RWE &amp; HEOR, Market Access, Omnichannel, Patient Support Programs, Syndicated Data and beyond.
 
 
You will develop and execute account strategies, build trusted senior-level relationships, and lead high-impact pursuits that help consumer health clients succeed in highly competitive and regulated markets.
 
 
What You&rsquo;ll Do 
 
&bull; Account ownership: Manage a portfolio of consumer health accounts across KSA, deliver on annual bookings and revenue targets.
 
&bull; New business development: Prospect for opportunities in strategy consulting, commercial planning, consumer insights, RWE/HEOR for OTC, E-commerce and digital health.
 
&bull; Solution shaping: Identify client challenges (e.g., category growth, Rx-to-OTC switches, consumer engagement, patient adherence, digital retail, supply chain optimization) and assemble the right IQVIA solution.
 
&bull; Multi-offering sales: Cross-sell IQVIA services&mdash;consulting, data subscriptions, syndicated audits, analytics platforms, technology solutions, real world evidence and Patient engagement.
 
&bull; Pipeline leadership: Lead end-to-end sales cycle: in collaboration with service team needs assessment, solution design, commercial modeling, negotiations, and contracting.
 
&bull; Client engagement: Develop and maintain relationships across marketing, medical, regulatory, commercial, and general business management functions.
 
&bull; Collaborate internally: Work closely with consulting partners, analytics, RWE, HEOR, technology/digital leads, and PSP teams to ensure integrated client solutions.
 
&bull; Market intelligence: Monitor consumer health and wellness market trends; translate insights into account opportunities.
 
&bull; Pipeline &amp; governance: Maintain disciplined CRM hygiene, ensure forecasting accuracy, and follow IQVIA compliance/ethical standards.
 
 
What You&rsquo;ve Done
 
 
&bull; 8&ndash;12 years in sales, business development, or consulting within Consumer Health / FMCG / Life Sciences sector, with at least 3&ndash;5 years in client-facing sales.
 
&bull; Demonstrated success selling consulting projects, syndicated data, technology platforms, or RWE/HEOR solutions to consumer health companies.
 
&bull; Understanding of consumer health dynamics (OTC, self-care, e-commerce, pharmacy channel, patient adherence, brand lifecycle, regulatory).
 
&bull; Track record of quota attainment and consistent pipeline building.
 
&bull; Strong commercial acumen; skilled in solution design, value articulation, and negotiation.
 
&bull; Strong presence with ability to influence senior stakeholders
 
&bull; Bachelor&rsquo;s degree required; MBA, MSc, or relevant advanced degree preferred.
 
&bull; Fluent English required; Arabic strongly preferred.
 
&bull; Willingness to travel up to 40-50%.
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 https://jobs.iqvia.com</div>

Senior Account Manager , Sales – Consumer Health (Life Sciences)

<div><div><div>External Job Description</div></div><div><div><div><div>
Job Overview:
Build SAP ERP technology solutions to support the Record to Report (RTR) functions such as General Ledger Accounting, Accounts Payable, Accounts Receivable, Bank Accounting, Asset Accounting, PS, SD-FI Integration, Cost Center Accounting, Profit Center Accounting &amp; Profitability Analysis, Reporting, Master Data Management, etc. Additionally, support Procure to Pay (PTP) functions such as Logistics Invoice Verification (LIV), GR Reconciliation, and MM-FI Integration.
Key Responsibilities:<ul><li>
Work with the project team, team leaders, project delivery leads, and client stakeholders to create FICO (RTR) &amp; LIV (PTP) solutions powered by SAP tools.</li><li>
Collaborate with team members across different time zones to implement regulatory solutions like SAF-T for countries such as Poland and Romania.</li><li>
Support bank integration for AR &amp; AP modules, including experience in DMEE &amp; EBS configuration.</li><li>
Act as an SME expert to translate project requirements, including features, user stories, and acceptance test criteria.</li><li>
Utilize domain knowledge to effectively synthesize input from multiple stakeholders to maximize delivered value.</li></ul>
Day-to-Day Responsibilities:<ul><li>
SAP Roadmap Development: Develop and maintain an SAP roadmap to deliver high-value/critical solutions to the business on time.</li><li>
Sprint Planning: Participate in sprint planning meetings to help define the main priorities for the team in the short, medium, and long term.</li><li>
Backlog Management: Prioritize and manage the SAP team backlog, ensuring it is up to date with major user stories, bug fixes, and other necessary items. This includes refining and clarifying requirements for the development team.</li><li>
Stakeholder Communication: Regularly communicate with stakeholders to gather requirements, receive feedback, and provide updates as appropriate.</li></ul>
Skills and Qualifications Required:<ul><li>
Bachelor&rsquo;s or master&rsquo;s degree in a relevant technical field (preferably CA/ICWA/MBA-Finance).</li><li>
SAP Certification in FICO would be an added advantage.</li><li>
Strong technical background with outstanding communication, presentation, time management, and leadership skills.</li><li>
Ability to manage stakeholder relationships effectively, both internally and externally, and communicate with diverse stakeholders.</li><li>
Experience as an SAP Consultant with at least 6 years of experience and multiple end-to-end SAP implementation projects.</li><li>
Proficient in all aspects of FICO, including the definition and assignment of Enterprise Structure, management of Master Data, E2E FICO &amp; PTP Process, and potential integration with external systems such as HFM, Blackline, Coupa, Concur, Ariba, MuleSoft, etc.</li></ul>
Technical Expertise:<ul><li>
General Ledger Accounting: GL Master Data, Journal Entry Posting, Manual &amp; Automatic Clearing, Period End Activities such as FCV, New GL &ndash; Parallel Ledgers &amp; Document Splitting.</li><li>
Accounts Payable: Vendor Master Data, PTP E2E Process from PR to MM Invoice, Automatic Payment Program, Vendor Down Payment, Partial Payment &amp; Extended Withholding Tax, MM-FI Integration, Logistics Invoice Verification (LIV), Special GL Transactions in AP, Input Tax, Payment Processing (Outgoing &ndash; Manual/Automatic).</li><li>
Accounts Receivable: Customer Master Data, SD-FI Integration, Customer Billing Functionality, Payment Processing (Incoming &ndash; Manual/Automatic), Special GL Transactions in AR &ndash; Downpayment, Bill of Exchange, Output Tax, Dunning, Interest Calculation, basic knowledge in FSCM Credit, Collections &amp; Dispute Management.</li><li>
Bank Accounting: Bank Master Data &amp; House Bank Configuration, experience in Lockbox, Cashed Check, Positive Pay File, EBS &amp; DMEE Configuration, and Search String Configuration.</li><li>
Asset Accounting: Asset Master Data, Asset Acquisition, Asset Transfers, Asset Retirement &amp; Depreciation Posting.</li><li>
Controlling: Basic knowledge in Cost Center Accounting (Cost Center, Activity Type &amp; Statistical Key Figure, Cost Center Hierarchy, Periodic Allocations and Reporting), Profit Center Accounting (Profit Center, Profit Center Hierarchy, Profit Center Actual Postings, Transfer Posting and Reporting), &amp; CO-PA Profitability Analysis (Structures in CO-PA, Value Fields, Characteristics, Characteristics Derivation, Actual Value Flows and Reporting).</li><li>
Proficiency in Incident Management and Change Management Processes.</li><li>
Excellent analytical and problem-solving skills with the ability to quickly diagnose and resolve complex issues.</li><li>
Ability to architect solutions in the SAP Finance &amp; Controlling functions by seamlessly integrating with other modules like SAP SD, MM, and BW functions.</li><li>
Offer expertise and comprehension of SAP FICO, Order to Cash, and Purchasing principles, as well as process flows, with the ability to grasp current configurations and suggest solutions for new requirements.</li><li>
Proven ability to work independently as well as part of a team in a fast-paced environment.</li></ul></div></div></div></div>
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 https://jobs.iqvia.com</div>

SAP FICO - Functional Consultant

<div><h1 class="jobSectionHeader">Primary Market Research Consultant
 </h1>IQVIA (www.iqvia.com) is a global human data science company focused on the pharmaceutical and biotechnology industry. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, technology, analytics, and human intelligence that bring the advances in data science together with the possibilities of human science.
The Custom Research team within IQVIA provides rapid, convenient, and effective communication between pharmaceutical companies, healthcare professionals and patients. We conduct market research studies to address critical strategic and tactical business questions faced by our biopharmaceutical clients. We employ a wide variety of methodologies to best address client objectives. Outstanding strategic thinking, analytical skills, and communication skills are essential to our business.
Job Summary:
We are hiring a Market Research Consultant to support primary research within our Data Processing team. This full-time role involves working closely with internal teams to deliver accurate, timely, and high-quality data deliverables. The ideal candidate is analytical, technically skilled in data processing tools, and thrives in a fast-paced environment with a strong focus on precision, efficiency, and meeting timelines.
Essential Duties and Responsibilities:
<ul><li>Act as single point of contact for data processing needs within assigned projects
</li><li>Analyze data using Q Research Software, SPSS, and Excel to meet project goals
</li><li>Prepare and manage datasets, including variables, weights, and statistical outputs
</li><li>Work closely with internal research teams to align objectives and ensure quality deliverables
</li><li>Deliver assigned tasks accurately and on time throughout the project lifecycle
</li><li>Support data validation and internal quality control processes
</li><li>Stay flexible with changing project needs while maintaining high standards and deadlines
</li><li>Collaborate across teams to ensure smooth execution and impactful insights
</li><li>Ensure compliance with client-specific and internal regulatory standards
</li></ul>Qualifications and Technical:
<ul><li>Bachelor&rsquo;s in computer science, Information technology, Statistics, Mathematics, or a related field
</li><li>Proficient in IBM SPSS and Microsoft Excel
</li><li>Hands-on experience with data analysis and tabulation tools such as Q Research, Displayr, MarketSight, Survey Reporter, Quantum, WinCross, or Askia
</li><li>Familiarity with JavaScript, Python, R, and VBA is a plus
</li><li>Strong foundation in mathematics and programming logic
</li></ul>Experience &amp; Core Competencies:
<ul><li>4.5+ years of experience in market research, including 2+ years in healthcare market research
</li><li>Proven project management skills with the ability to handle multiple projects under tight deadlines
</li><li>Strong analytical and problem-solving abilities with keen attention to detail
</li><li>Exposure to healthcare data sources, HCP/patient data, or global health markets is an advantage
</li><li>Adaptable to changing project requirements while maintaining high-quality output
</li></ul>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 https://jobs.iqvia.com</div>

Primary Market Research Consultant ( Data Processing )

<div>Job Overview
The medical department consists of a Chief Medical Officer, Medical Directors, Sr 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
Functions as project team member:
<ul><li>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.
</li><li>Ensures medical activities run according to GCP and operate with highest efficiency.
</li><li>Establishes and maintains a network of medical/scientific consultants, etc.
</li><li>Supervises and manages Medical Director activities.
</li></ul>Clinical Activities:
<ul><li>Interacts with clients regarding drug development programs, study design and protocol.
</li><li>Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
</li><li>Interacts in team approach to develop statistical and data management sections of the protocol.
</li><li>Reviews the final protocol for clinical, safety and efficacy variables.
</li><li>Provides project team training on protocol and/or therapeutic areas.
</li><li>Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
</li><li>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.
</li><li>Presents protocol and/or safety reporting information at investigator meetings.
</li><li>Develops project medical monitoring plans as requested.
</li><li>Assist the team and sites in responding to protocol-related or study-related or medical questions.
</li><li>Assist site staff with urgent and non-urgent safety events, and provide recommendations in accordance with the protocol.
</li><li>Provides on call coverage for protocol queries and site support.
</li><li>Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
</li></ul>Safety Monitoring and SAE Reporting Activities:
<ul><li>Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
</li><li>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.
</li><li>Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
</li><li>In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
</li><li>Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
</li></ul>Data Activities:
<ul><li>Provides medical review of eCRFs for clinical accuracy.
</li><li>Provides medical review of data analysis plan.
</li><li>Reviews safety fields at case freeze for reconciliation (if needed).
</li><li>Works with data group to reconcile SAE events as needed.
</li><li>Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
</li><li>Reviews data tables, listings, and figures.
</li><li>Reviews and/or writes portions of final clinical study report.
</li></ul>DSMB/Adjudication Committee Activities:
<ul><li>May assist sponsor in choosing committee members.
</li><li>May serve as a non-voting member to convene and organize proceedings.
</li><li>May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
</li><li>May determine data flow with sponsor to ensure reporting accuracy.
</li><li>Can ensure DSMB feedback is given to sites for IRBs.
</li><li>All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
</li></ul>Business Development Activities:
<ul><li>Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
</li><li>Supports business development activities with proposal development and sales presentations.
</li><li>Participates in feasibility discussions relating to specific project proposals.
</li></ul>Special Projects:
<ul><li>Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
</li><li>Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
</li><li>Participate in a variety of team quality improvement efforts as necessary.
</li><li>Perform other related duties as assigned or requested by the Chief Medical Officer.
</li></ul>Qualifications
<ul><li>Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
</li><li>10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
</li><li>3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
</li><li>Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
</li><li>Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
</li><li>Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
</li><li>Excellent oral and written communications skills as well as interpersonal skills are essential.
</li></ul>Oncology / Hematology
<ul><li>Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
</li><li>Board Certified / Board Eligible: Hematology (Required)
</li><li><h2 class="jobSectionHeader">Applicants must have experience in at least one of the following areas: Hematology (Non-Malignant) , Hematological Malignancies , Pediatric Hematology / Adult Hematology
</h2></li></ul>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 https://jobs.iqvia.com</div>

Medical Director - Hematology , Home- Based

<div>Job Overview
The medical department consists of a Chief Medical Officer, Medical Directors, Sr 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
Functions as project team member:<ul><li>
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.</li><li>
Ensures medical activities run according to GCP and operate with highest efficiency.</li><li>
Establishes and maintains a network of medical/scientific consultants, etc.</li><li>
Supervises and manages Medical Director activities.</li></ul>
Clinical Activities:<ul><li>
Interacts with clients regarding drug development programs, study design and protocol.</li><li>
Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.</li><li>
Interacts in team approach to develop statistical and data management sections of the protocol.</li><li>
Reviews the final protocol for clinical, safety and efficacy variables.</li><li>
Provides project team training on protocol and/or therapeutic areas.</li><li>
Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.</li><li>
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.</li><li>
Presents protocol and/or safety reporting information at investigator meetings.</li><li>
Develops project medical monitoring plans as requested.</li><li>
Assist the team and sites in responding to protocol-related or study-related or medical questions.</li><li>
Assist site staff with urgent and non-urgent safety events, and provide recommendations in accordance with the protocol.</li><li>
Provides on call coverage for protocol queries and site support.</li><li>
Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.</li></ul>
Safety Monitoring and SAE Reporting Activities:<ul><li>
Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.</li><li>
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.</li><li>
Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.</li><li>
In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).</li><li>
Interact with appropriate FDA officials concerning safety and other study related issues, as requested.</li></ul>
Data Activities:<ul><li>
Provides medical review of eCRFs for clinical accuracy.</li><li>
Provides medical review of data analysis plan.</li><li>
Reviews safety fields at case freeze for reconciliation (if needed).</li><li>
Works with data group to reconcile SAE events as needed.</li><li>
Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.</li><li>
Reviews data tables, listings, and figures.</li><li>
Reviews and/or writes portions of final clinical study report.</li></ul>
DSMB/Adjudication Committee Activities:<ul><li>
May assist sponsor in choosing committee members.</li><li>
May serve as a non-voting member to convene and organize proceedings.</li><li>
May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.</li><li>
May determine data flow with sponsor to ensure reporting accuracy.</li><li>
Can ensure DSMB feedback is given to sites for IRBs.</li><li>
All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.</li></ul>
Business Development Activities:<ul><li>
Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.</li><li>
Supports business development activities with proposal development and sales presentations.</li><li>
Participates in feasibility discussions relating to specific project proposals.</li></ul>
Special Projects:<ul><li>
Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.</li><li>
Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.</li><li>
Participate in a variety of team quality improvement efforts as necessary.</li><li>
Perform other related duties as assigned or requested by the Chief Medical Officer.</li></ul>
Qualifications<ul><li>
Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.</li><li>
10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.</li><li>
3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.</li><li>
Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.</li><li>
Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.</li><li>
Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.</li><li>
Excellent oral and written communications skills as well as interpersonal skills are essential.</li></ul>
Oncology / Hematology<ul><li>
Current or prior license to practice medicine; board certification/eligibility ideal (Preference)</li><li>
Board Certified / Board Eligible: Hematology (Required)</li><li><h2 class="jobSectionHeader">
Applicants must have experience in at least one of the following areas: Hematology (Non-Malignant) , Hematological Malignancies , Pediatric Hematology / Adult Hematology</h2></li></ul>
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 https://jobs.iqvia.com</div>

Join IQVIA and explore 25   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

IQVIA

ABOUT_COMPANY

Software QA Engineer

Senior Account Manager , Sales – Pharma (Life Sciences)

Senior Account Manager , Sales – Consumer Health (Life Sciences)

SAP FICO - Functional Consultant

Primary Market Research Consultant ( Data Processing )

Medical Director - Hematology , Home- Based

Medical Director - Hematology , Home- Based