Urwah Admin

IQVIA

<div>Job Overview
 
Principal Data Manager position is to oversee data operations tasks for a team of data managers from study start-up to database lock, to produce a clean and analyzable database.
<div>Essential Functions
 
<ul><li>Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies
</li><li>Provide leadership to CDM team.
</li><li>Manage CDM customer relationship for CDM project team to include leading (with minimal guidance) CDM customer negotiations on complex timeline, budgetary and other issues.
</li><li>Provide marketing capabilities presentations and business development presentations. . Or serve as Data Operations Coordinator (DOC) for one or three global clinical trials with fewer than 25 operations staff (excludes DE) or 20-40 central laboratory studies, or serve in a leadership role to a specific DM Task.
</li><li>Serve as back-up for Data Operations Coordinator or Data Team Lead
</li><li>Provide leadership to Operations team
</li><li>Provide technical expertise. Or serve as a Subject Matter Expert (SME)
</li><li>Provide leadership and expertise in a specific CDM task or technology. Manage delivery of projects through full data management process life-cycle.
</li><li>Management of:
</li><li>Project timelines
</li><li>Quality issues
</li><li>Resource management
</li><li>SOW (scope of work) / budget. Provide justification for customer negotiations. May serve as Project Manager for single service data management projects. Manage comprehensive data management tasks pertaining to the documented project specifications. Manage comprehensive quality control procedures. Provide data management expertise and data management process improvement to CDM management. Mentor other team members in training and developing data management expertise. Independently bring project solutions to the CDM team and the CDM Department. Manage a focus team or a best practice team. Manage the development and implementation of new technology/tool. Present at professional conferences and/or publish articles in professional journals. Provide CDM with technical expertise. Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions. Perform other duties as directed by the functional manager. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM and project teams.&quot;
</li></ul></div><div>Qualifications
 
<ul><li>Bachelor's Degree clinical, biological or mathematical sciences, or related field or nursing qualification Req
</li><li>5 years relevant experience including proven competence in managing delivery of multiple projects simultaneously through full data management study life-cycle, including large trials &gt;1000 patients, and including experience handling customer negotiations (e.g. bid defense meetings). Equivalent combination of education, training and experience.
</li><li>Thorough knowledge of the data management process and experience in specialized data management skills (e.g., therapeutic, extensive knowledge, SAE reconciliation, central laboratory, and/or new technology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Excellent experience and organizational, communication, and demonstrated expert data management skills. Comprehensive understanding of clinical drug development process (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients. Thorough knowledge of the data management process and experience in specialized data management skills (e.g., therapeutic, extensive knowledge, SAE reconciliation, central laboratory, and/or new technology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Excellent experience and organizational, communication, and demonstrated expert data management skills. Comprehensive understanding of clinical drug development process (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients.
</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>

Senior Data Strategist

<div>Job Overview 
Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. Perform role of Data Team Lead (DTL). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.<div>
Essential Functions 
<ul><li>Client Management:. serve as primary point of contact for customer on data management deliverables. With minimal guidance, provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise. With guidance, provide input for and perform direct negotiations with customer, e.g., timelines, financial, process, resources. Maintain strong customer relationships. Ensure open communications with customer and IQVIA management to manage and meet contractual obligations. Service Management:. Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables. Establish strong communications with Data Operations team, functional leads, project managers and all other stakeholders. With minimal guidance, support DM service delivery with comprehensive DM process and technical expertise in executing projects. Serve as the escalation point for unresolved data issues</li><li>with guidance, work with client data managers, vendors, internal team members for resolution. Work with functional manager(s) to ensure appropriate resources are assigned to meet project deliverables. With guidance, create and/or review and sign-off on all data management plan (DMP) documents. Implement proactive quality management plan. Identify any service and quality issues with agreed upon specifications per the DMP and contract/SOW and work with functional manager(s) to resolve. With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions. Continuously look for opportunities to improve efficiency of tasks and quality of deliverables. Identify compliance issues and work with functional manager(s) to ensure timely follow-up and resolution. With guidance, maintain internal tracking databases and systems. Financial Management/Business Development Support:. With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW). Manage SOW/budget. - Review financial reports on a monthly basis and participate in project reviews as requested. - Identify out of scope tasks and track change orders to completion. With guidance, may serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing. With guidance, participate in and support RFP process (review RFP documents, pricing, attend bid defense). Other:. Provide input on DM process improvements or project solutions to CDM team/CDM department. Provide input on the development and implementation of a new technology or tool. Participate in a focus team or global or local best practice team. Perform other duties as directed by functional manager(s)</li></ul></div><div>
Qualifications 
<ul><li>Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management. Req</li><li>1-2 years of direct Data Management experience with a minimum of 6 months as a CDM project lead Pref</li><li>Previous experience and proven competence in managing study delivery through full DM life-cycle (at least 1 medium Phase III). Demonstrated data management skills and thorough knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and applicable regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work with minimal supervision, using available resources, e.g., functional managers, senior DTLs. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers. Previous experience and proven competence in managing study delivery through full DM life-cycle (at least 1 medium Phase III). Demonstrated data management skills and thorough knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and applicable regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work with minimal supervision, using available resources, e.g., functional managers, senior DTLs. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers.</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>

Data Team Lead

<div>Job Overview 
Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor&rsquo;s requirements.
Essential Functions<ul><li>
Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations. Responsible for delivery on established targets/measurements.</li><li>
Work with global teams to review and analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions. Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Escalate as appropriate.</li><li>
Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.</li><li>
Participate in discussions related to the development of site/investigator budgets aligned with fair market value.</li><li>
Manage the contract amendment lifecycle.</li><li>
Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.</li><li>
Assume responsibility for all aspects of legal document and metrics tracking.</li><li>
Provide support to review, authorize and/or understand aspects of site payments. Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.</li><li>
Track all aspects of legal document and metrics. Determine potential needs for contract amendments and manage amendment lifecycle.</li></ul>
Qualifications<ul><li>
Bachelor&rsquo;s degree in related field</li><li>
3 years&rsquo; experience and/or equivalent competencies in legal/ pharmaceutical industry/clinical research.</li><li>
Excellent communication skills (both oral and written).</li><li>
Familiarity with healthcare compliance and other relevant guidance</li><li>
Familiarity with clinical research processes.</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>

Contract Negotiator (FSP) - Turkey

<div>Clinical Specialist Consultant - Turkish Speaking 
Location: Remote/virtual
Hours: Estimated 10-16h/month
Role: Clinical Specialist 
Job Description:
The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is evaluated, and live interaction with raters is conducted to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Other Clinical Specialist responsibilities may include, but are not limited to, functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications. 
Required Experience, Knowledge, Skills:<ul><li>Minimum of a master&rsquo;s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent. MD, DO or PhD preferred</li><li>Minimum of 3 years&rsquo; experience administering psychiatric assessments, ratings scales and/or structured clinical interviews. Specifically, MADRS/SIGMA; CGI-S, C-SSRS, HDRS-17, ISI and PHQ-9</li><li>Minimum of 3 years clinical experience with related psychiatric populations.</li><li>Minimum of 3 years experience with administering scales in clinical research trials (not including graduate/doctoral research work).</li><li>Experience in central nervous system (CNS) trials preferred.</li><li>Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.</li><li>Excellent organization, attention to detail, time management and problem-solving skills.</li><li>Computer proficiency with Windows and Microsoft Office system and applications.</li></ul> 
Tasks/Responsibilities:<ul><li>Participate in all orientation, training and calibration activities as required.</li><li>Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).</li><li>Complete rater interactions and assigned tasks as scheduled.</li><li>Responsible for timely submission of all documentation associated with assigned tasks.</li></ul><ul><li> 
Current openings require fluency in English and a native speaker in the language needed for the trial.</li></ul> 
#LI-DNP #LI-Remote #LI-HCPN
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>

Clinical Trial Psych Rater - Turkish Speaking

<div>Clinical Specialist Consultant - Turkish Speaking
Location: Remote/virtual
Hours: Estimated 10-16h/month
Role: Clinical Specialist
Job Description:
The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is evaluated, and live interaction with raters is conducted to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Other Clinical Specialist responsibilities may include, but are not limited to, functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.
Required Experience, Knowledge, Skills:
&bull; Minimum of a master&rsquo;s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent. MD, DO or PhD preferred
&bull; Minimum of 3 years&rsquo; experience administering psychiatric assessments, ratings scales and/or structured clinical interviews. Specifically, MADRS/SIGMA; CGI-S, C-SSRS, HDRS-17, ISI and PHQ-9
&bull; Minimum of 3 years clinical experience with related psychiatric populations.
&bull; Minimum of 3 years experience with administering scales in clinical research trials (not including graduate/doctoral research work).
&bull; Experience in central nervous system (CNS) trials preferred.
&bull; Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.
&bull; Excellent organization, attention to detail, time management and problem-solving skills.
&bull; Computer proficiency with Windows and Microsoft Office system and applications.
Tasks/Responsibilities:
&bull; Participate in all orientation, training and calibration activities as required.
&bull; Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).
&bull; Complete rater interactions and assigned tasks as scheduled.
&bull; Responsible for timely submission of all documentation associated with assigned tasks.
*Current openings require fluency in English and a native speaker in the language needed for the trial. 
 
 
#LI-DNP #LI-Remote #LI-HCPN
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>

<div>
 High quality, patient-centered data is becoming an increasing imperative for our clients, regulators and other stakeholders to understand whether a drug provides treatment or safety benefit. We have an exciting opportunity for an experienced Life Science Consultant to join our Patient Centered Solutions consulting team.
 
 
 In this role you&rsquo;ll work closely with project lead/global clients, supporting &lsquo;Patient Centered Solutions&rsquo; research-based projects, that will inform PRO (Patient-Reported Outcomes)/COA (Clinical Outcome Assessment) strategies for clinical and real-world studies
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 Perform extensive research and analysis to build a detailed understanding of the patient experience with a disease and intervention to inform a PRO/COA strategy
 </li>
 <ul>
 <li>
 Source information based on robust targeted literature review methods, social media and patient interview transcript analysis
 </li>
 </ul>
 <li>
 Contribute to project teams in the development and delivery of client deliverables including analysis of IQVIA and public information sources, conducting primary research and independent secondary research
 </li>
 <li>
 Participating in internal and client meetings and supporting the presentation of project findings to the client
 </li>
 <li>
 Undertake indication COA landscape assessments to understand key stakeholder demands for patient experience data and how endpoints are being deployed into clinical study designs
 </li>
 <ul>
 <li>
 Source information using secondary research methods covering open-source databases and subscription services
 </li>
 </ul>
 <li>
 Identify and summarise the characteristics of available COA/PRO instruments to measure a specified disease or treatment experience using subscription databases and targeted publication searches
 </li>
 <li>
 Document and report research in Word and PowerPoint using independent, critical thinking to ensure quality and completeness of output
 </li>
 <ul>
 <li>
 Good public domain searching skills to mine information on various pharma topics
 </li>
 </ul>
 <li>
 Experience in Pharma qualitative analytics, disease landscape assessment, competitive environment, clinical trials analysis, pipeline analysis, treatment algorithms, regulatory environment understanding etc.
 </li>
 <li>
 Supporting global PCS team to elevate our capabilities, including (but not limited to) the development of intellectual property, marketing materials, training, recruitment and other BD activities
 
 </li>
 </ul>
 
 Education &amp; Experience:
 
 
 
 <ul>
 <li>
 Graduate/Post-graduate Degree in Life Sciences from a premier institute (PharmD, MBBS, BDS, Bpharm, Mpharm, Clinical Research etc.)
 </li>
 <li>
 2-6 years of experience within Pharmaceutical/ Biotechnology/ Consulting/ Professional Services Outsourcing company
 </li>
 <li>
 Ability to understand clinical trial designs, outcome measures, endpoints, and results
 </li>
 <li>
 Previous experience with literature reviews and scientific writing is an added advantage
 </li>
 <li>
 Excellent oral and written communication skills
 </li>
 <li>
 Must be proficient in Word, Excel, PowerPoint and Internet Explorer
 </li>
 <li>
 Experience with programmes such as ATLAS.ti or MAXQDA is an advantage
 
 
 </li>
 </ul>
 
 Additional Requirements:
 
 
 
 <ul>
 <li>
 Well-developed written and verbal communication skills including presentations, workshop facilitation, and report writing
 </li>
 <li>
 Ability to establish and maintain effective working relationships with co-workers, managers and clients in a global and matrixed environment.
 </li>
 <li>
 Ability to structure project research approach synthesize qualitative and quantitative data from public domain and IQVIA datasets and draw meaningful insights
 </li>
 <li>
 Strong grasp of research methodologies and their merits/shortcomings
 </li>
 <li>
 Deliver high quality, client-ready output with minimal supervision; identify risks / issues and escalate to the project leads in a timely manner
 </li>
 <li>
 High sensitivity to deadlines
 </li>
 <li>
 Understanding of global healthcare environment
 </li>
 <li>
 High consciousness towards attention to detail; drive and commitment towards delivering high quality work
 </li>
 <li>
 Self-motivated, with strong work ethics; proactive in identifying issues and opportunities and delivering insightful solutions
 </li>
 <li>
 Support knowledge management, quality and process improvement
 </li>
 <li>
 A passion to develop skills that will support driving Patient Science forward
 
 
 </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>

Associate Consultant

<div>159 Solutions (Consulting) &ndash; Analyst About Company: 159 Solutions (an IQVIA company) is a Healthcare consulting firm that delivers a wide range of analytical solutions to Life Sciences clients to help them drive customer value and company results. We leverage our deep industry expertise coupled with thoughtful data analysis to provide customized solutions that work in the real world. We believe in delighting our customers and greatly value our people, their perspectives and new ideas. 159 Solutions has 150+ talented and motivated people working in Pune, India collaborating with our colleagues in California &amp; New York serving life sciences companies in US. Role &ndash; Analyst Analysts are active participants in analyzing the data and creating solutions for our clients to solve business problems across various practice areas such as promotion response modeling, patient claims analytics, sales force strategy, incentive compensation, business intelligence, data modeling etc. Key Responsibilities &bull; Analyze the data and design custom solutions to uncover insights and solve client&rsquo;s problem &bull; Process large-scale healthcare datasets using Excel, SQL, Alteryx, other database management tools &bull; Develop recommendations for the client and create PowerPoint slides or online visualization (e.g. Tableau, PowerBI, Sisense etc.) to communicate results to clients and internal teams &bull; Collaborate with internal teams and others to learn new skills Qualifications &bull; Bachelor's degree in any engineering discipline Individuals should also have the following personal skills: &bull; High motivation, strong work ethic and positive attitude &bull; Strong problem-solving skills &bull; Adaptive learner with dedication to continuous learning &bull; Client service orientation with focus on quality and detail &bull; Excellent task management skills &bull; Effective time management skills &bull; Good communication skills with fluency in English &bull; Ability to work across global cross-office teams IQVIA offers a competitive compensation package with salary and bonus incentives, plus an attractive benefits package.
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>

Analyst

Join IQVIA and explore 9   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

Senior Data Strategist

Data Team Lead

Contract Negotiator (FSP) - Turkey

Clinical Trial Psych Rater - Turkish Speaking

Clinical Trial Psych Rater - Turkish Speaking

Associate Consultant

Analyst