Urwah Admin

IQVIA

<div><div><div>Valencia, United States of America | Full time | Office-based | R1528337</div></div><p></p><div><div><div><br>
We are seeking a <b>Pre-Analytical Services Associate, Lab Services</b> to join IQVIA&rsquo;s laboratory business at <b>Valencia, CA</b>.</div><div><b>
Shift: Tuesday-Saturday 9am-530pm
</b></div><div>In this role, you will assist with routine activities related to the receipt and processing of clinical specimens, ensuring accuracy, compliance, and timely workflow.</div><div>
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.</div><h3 class="jobSectionHeader"><b>
What You&rsquo;ll Be Doing:</b></h3><ul><li>
Assist with receipt of consignments and shipments.</li><li>
Open shipments and perform quality checks on patient information forms; escalate issues to senior staff.</li><li>
Dispose of or recycle kit shipping supplies appropriately.</li><li>
Conduct secondary checks to ensure specimens are not left in kit packaging.</li><li>
Support and respond to after-hour alarms and other critical functions.</li><li>
Assist with equipment maintenance and supply inventory functions.</li><li>
Perform administrative duties and maintain organized work areas.</li><li>
Follow safety procedures and participate in continuing education activities.</li></ul><h3 class="jobSectionHeader"><b>
What We Are Looking For:</b></h3><ul><li>
High School Diploma or equivalent required.</li><li>
Basic computer skills and ability to maintain accurate reporting procedures.</li><li>
Strong organizational skills and ability to manage workflow effectively.</li><li>
Other Equivalent combination of education, training, and experience may be accepted in lieu of degree.</li></ul><h3 class="jobSectionHeader"><b>
The Knowledge, Skills and Abilities Needed for This Role:</b></h3><ul><li>
Ability to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures.</li><li>
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li><li>
Attention to detail and accuracy in handling specimens and documentation.</li><li>
Good organizational and communication skills for team collaboration.</li></ul><h3 class="jobSectionHeader"><b>
What We Offer You:</b></h3><div>
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&rsquo; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</div><div>
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.</div><div>
If you&rsquo;re looking to unleash your potential, join Q2 Solutions, IQVIA&rsquo;s laboratory business, to help make the extraordinary possible!</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role, when annualized, is $24,400.00 - $50,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

Pre-Analytical Services Associate • Lab Services

<div><div><div>Northborough, United States of America | Full time | Office-based | R1537347</div></div><p></p><div><div><br>
A Pharmacy Technician assists the pharmacist with various aspects of order processing to dispense medications to patients as promised in an accurate, safe and efficient manner. A Pharmacy Technician plays a critical role in proving patients and providers access to medications needed.</div><div><b>
This role is onsite at our Northborough office. Pharmacy hours are 8am-6pm, so hours are flexible within that time frame.</b></div><div>
The information contained herein is intended to be an accurate reflection of the duties and responsibilities of the individuals assigned to this position. They are not intended to be an exhaustive list of the skills and abilities required to do the job. AllCare Plus Pharmacy reserves the right to revise the job or to require that other or different tasks be performed as assigned.</div><div><b>
Primary Responsibilities:</b></div><div>
1. Register new patients into pharmacy systems with appropriate program designations</div><div>
2. Type new prescription orders into the pharmacy system</div><div>
3. Answer in-bound calls to assister patients, providers and internal patient support services with inquiries</div><div>
4. Perform outbound calls to patients and providers to welcome to pharmacy and for refill prescription scheduling</div><div>
5. Escalate questions around medication usage and concerns to the pharmacist</div><div>
6. Facilitate scheduling for prescription delivery to patient or provider&rsquo;s office</div><div>
7. Maintain current patient profiles per accreditation requirements as well as State and Federal regulations and laws</div><div>
8. Obtain and complete prescription transfers to and from other pharmacies as needed</div><div>
9. Assist in prescription order requests from providers and clarification on prescriptions under the supervision of a pharmacist.</div><div>
10. Process scheduled order- fulfillment and facilitate the process of urgent orders to ship as promised</div><div>
11. Provide customers with courteous, friendly, fast and efficient service</div><div><b>
Additional Responsibilities:</b></div><div>
1. Utilize headset and computer terminal and navigate through multiple systems to input and retrieve information.</div><div>
2. Update job knowledge by participating in educational opportunities and training activities</div><div>
3. Work efficiently both individually and within a team to accomplish required tasks</div><div>
4. Maintain and improve quality results by adhering to standards and guidelines; recommending improved procedures</div><div><b>
Required Qualifications:</b></div><div>
1. High School Diploma or equivalent</div><div>
2. Minimum one year of Pharmacy Technician or relative work experience</div><div>
3. RPhT Pharmacy Technician License or National (CPhT) Pharmacy Technician Certification</div><div>
4. CPhT position requires a minimum of twenty (20) CE hours in pharmacy-related subject matter during each two (2) year recertification cycle</div><div>
5. Previous data entry experience and ability to type 30wpm+</div><div><b>
Professional Competencies:</b></div><div>
1. Business Skills and Knowledge</div><ul><li>General Management</li></ul><div>
Demonstrate analytic and problem solving skills, and understand the impact of individual decisions on other parts of the organization and the environment.</div><ul><li>Information management</li></ul><div>
An understanding of how technology can be used to promote managerial and clinical efficiency and improve health care delivery. The ability to effectively manage</div><div>
information resources and plan for future needs.</div><ul><li>Quality improvement</li></ul><div>
Application of techniques that continually improve the quality of care provided, patient safety, organizational performance, and the financial health of the organization.</div><div>
2. Knowledge of the Health Care Environment</div><ul><li>Health Care Systems and Organizations</li></ul><div>
Demonstrate an understanding of how the various components of the health care system is organized and financed, and how they interact to deliver medical and health care.</div><ul><li>The Patient&rsquo;s Perspective</li></ul><div>
Understand the patient experience, demonstrate a commitment to patients&rsquo; rights and responsibilities, and ensure that the organization provides a safe environment for patients and their families.</div><div>
3. Communication and Relationship Management</div><ul><li>Relationship Management</li></ul><div>
The ability to build and maintain relationships with internal as well as external</div><div>
stakeholders that are anchored in trust and where decision-making is shared.</div><ul><li>Communication Skills</li></ul><div>
Be able to utilize verbal, written and presentation skills to communicate an</div><div>
organization&rsquo;s mission, vision, values and priorities to diverse audiences.</div><div>
4. Professionalism</div><ul><li>The ability to align personal and organizational conduct with ethical and professional standards that include a responsibility to the patient and community, a service orientation, and a commitment to lifelong learning and improvement.</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is $20.00-$25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

Pharmacy Technician – Hybrid

<div><div><div>Fairfax, United States of America | Full time | Office-based | R1536651</div></div><p></p><div><div><b><br>
Job Location</b><br>
Office-based in Fairfax, VA<br>
</div><div><b>Job Summary</b></div><div>
Under the direction and supervision of the Director of Clinical Trial Management, this position is responsible for the preparation, scanning, labeling and maintenance of medical records for the practice. The position works closely with the research team in support of all ongoing clinical studies.</div><div><b>
Essential Duties and Responsibilities</b></div><ul><li><div>
Demonstrates an understanding of patient/sponsor confidentiality to protect the patient and practice</div></li><li><div>
Creates and maintains the patient medical record for each patient; in electronic format and in paper, as needed.</div></li><li><div>
Following HIPAA guidelines gathers patient records from a variety of sources (i.e., mail, fax/eFax, email, etc.), which will require interacting with registration areas and/or physicians' office's in a professional manner.</div></li><li><div>
Scans and attaches medical records into the electronic medical record system according to guidelines.</div></li><li><div>
Keeps practice health care providers informed by communicating availability or unavailability of the record.</div></li><li><div>
Handles medical record requests and patient care related releases of information ensuring that all releases are compliant with HIPAA guidelines.</div></li><li><div>
Assists in purging deceased and inactive charts as scheduled and according to guidelines.</div></li><li><div>
Ability to assist in the guidance and training of less experienced staff. &bull; Ability to maintain a positive attitude with the research team.</div></li><li><div>
Remains current with all required</div></li></ul><div><b>
Knowledge, Skills and Abilities</b></div><ul><li><div>
Excellent interpersonal skills to deal effectively with research personnel</div></li><li><div>
Knowledge of medical terminology.</div></li><li><div>
Knowledge of HIPAA guidelines.</div></li><li><div>
Excellent organizational skills to independently manage workflow.</div></li><li><div>
Ability to prioritize quickly and appropriately with minimal guidance.</div></li><li><div>
Ability to multi-task.</div></li><li><div>
Ability to work independently and function as part of a team.</div></li><li><div>
Clear and concise verbal and written communications.</div></li><li><div>
Excellent attention to detail.</div></li><li><div>
High school graduate or GED</div></li></ul><div><b>
Required Education and Experience</b></div><ul><li><div>
High school diploma or GED</div></li></ul><div><b>
Why Join Us?</b></div><div>
At NEXT Oncology (an Avacare Business), you&rsquo;ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role, when annualized, is $25,900.00 - $64,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

Medical Records Clerk

<div><div><div>Carlsbad, United States of America | Part time | Field-based | R1537301</div></div><p></p><div><h2 class="jobSectionHeader"><b><br>
Qualified </b><b>Ultrasound Sonographer</b><b> will be tasked with educating end users on a ultrasound machine used in hospital facilities and other healthcare facilities.</b></h2><h2 class="jobSectionHeader"><b>
You are responsible for end-user education and being a strong promoter of the product and company, you represent is highly valued. This Product Application Specialist role allows you to utilize your experience in a new way that does not involve direct patient care. Depending on your current schedule, this type of role can work in conjunction with your current position. Additionally, you will receive exposure to the ultrasound industry with the potential for long-term career growth in the field.</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Your primary focus will be in-servicing and education only; no sales responsibilities, and no bedside care.</b></h2></li><li><h2 class="jobSectionHeader"><b>
A desire to expand your talents in clinical education.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Travel local, regionally and nationally to support customer needs.</b></h2></li><li><h2 class="jobSectionHeader"><b>
Appropriate PPE is provided to all employees prior to the start of assignments.</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Job Responsibilities:</b></h2><h2 class="jobSectionHeader"><b>
Provide peer-to-peer education and consultation to Ultrasound Sonographers and other healthcare staff in support of end-user education needs in the healthcare setting.</b></h2><h2 class="jobSectionHeader"><b>
Assess customer needs and assist with resolving issues stemming from lack of product knowledge or understanding of the particular product.</b></h2><h2 class="jobSectionHeader"><b>
Assist in the delivery of ultrasound-related in-service education to support key customers.</b></h2><h2 class="jobSectionHeader"><b>
Follow-up with key accounts and customers to assess unmet education and clinical needs as it relates to successful ultrasound machine implementation.</b></h2><h2 class="jobSectionHeader"><b>
Schedule:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Per-diem position requiring travel and flexibility to work with your current schedule.</b></h2></li><li><h2 class="jobSectionHeader"><b>
2 weeks minimum of availability a month, more days preferred.</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Required Qualifications:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Ultrasound Sonographer with POC experience, Cardiovascular or General Imaging US (Radiology)</b></h2></li><li><h2 class="jobSectionHeader"><b>
One of the following Credentials required: ARDMS, RDCS, CCI</b></h2></li><li><h2 class="jobSectionHeader"><b>
3+ years of experience as an Ultrasound Sonographer</b></h2></li><li><h2 class="jobSectionHeader"><b>
Must be comfortable with basic software programs</b></h2></li><li><h2 class="jobSectionHeader"><b>
Customer Focused</b></h2></li><li><h2 class="jobSectionHeader"><b>
Demonstrate professional interpersonal skills, both oral and written</b></h2></li><li><h2 class="jobSectionHeader"><b>
Demonstrate excellent teaching skills</b></h2></li><li><h2 class="jobSectionHeader"><b>
Duties may require compliance with client requirements that all those performing services on-site be fully vaccinated</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Preferred Qualifications:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
Associate's Degree required, Bachelor's Degree preferred</b></h2></li><li><h2 class="jobSectionHeader"><b>
Leadership experience (manager, educator, preceptor) can be helpful but is not required</b></h2></li></ul><h2 class="jobSectionHeader"><b>
Benefits:</b></h2><ul><li><h2 class="jobSectionHeader"><b>
This position is not eligible for our Medical Benefits.</b></h2></li></ul><h2 class="jobSectionHeader"><b>
IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.</b></h2><h2 class="jobSectionHeader"><br>
<b>
Vaccine/Immunization/Hospital</b><b> Credentialing Requirement</b><b>: A required function of this job requires individuals to enter various healthcare facilities. Thus, upon selection, individuals must complete healthcare facility credentialing process. To obtain credentials, individuals must meet the immunization requirements specified by the facility. Individuals are typically required to have completed/up to date: Measles, Mumps &amp; Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria &amp; Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client&rsquo;s requirements may supersede this.
</b><br>
</h2><ul><li><b>Please note: Due to the nature of this role, it is not eligible for Visa sponsorship.</b></li></ul><h2 class="jobSectionHeader"><b>
#LI-DNP
</b></h2><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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is 70 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

MedTech Market Research Project OB Sonographer - Channahon, IL

<div><div><div>Rosemont, United States of America | Full time | Home-based | R1530148</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><b><br>
About the Team:</b></div><div>
At IQVIA, our Patient Centered Solutions (PCS) team is dedicated to integrating the patient voice into medical research and development. Our scientific consulting services group conducts qualitative, quantitative, and mixed methods studies to better understand the patient, clinician, or caregiver experience.</div><div>
Projects range in size, type, and across multiple disease areas, and include clinical outcome assessment (COA) development, modification, and validation to support medical product development; strategic consulting for regulatory needs; exploratory analyses of existing data; literature review and gap analysis; and non-interventional studies with conceptualization, primary data collection via qualitative and/or quantitative methods, analysis, interpretation/synthesis, and dissemination phases. You'll enjoy a rewarding career in a collaborative, multicultural environment that values growth and development.</div><div><b>
Role Overview</b>:</div><div>
Join IQVIA as a Manager and play a key role in executing and delivering on primary literature reviews, data collection efforts, and analysis/reporting of qualitative and/or quantitative data. Your expertise will support customers in life science and population health markets with patient reported outcome (PRO) and other COA solutions, and will directly influence the success of clinical trials and patient-centered, observational studies. In this role, you will be responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. You will also identify and elevate potential new business opportunities and assist in the business development and proposal process. You will also receive the training, mentorship, and additional experience needed to advance in a research career track.</div><div><b>
Key Responsibilities</b>:</div><ul><li>
Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects, leveraging primarily qualitative or mixed-methods approaches.</li><li>
Reviews and analyzes client requirements or problems and assists in the development of proposals of cost-effective solutions that ensure profitability and high client satisfaction.</li><li>
Provides direction and guidance to Consultants, and where relevant, to Statistical Services assigned to engagement on overall project objectives, client needs, and scientific execution of the project with assistance from subject matter experts (SMEs).</li><li>
Develops or oversees development of detailed documentation and specifications, including protocol and study document development.</li><li>
Performs or oversees qualitative analyses to assist in the reporting of studies to address client needs and the development of client specific solutions.</li><li>
Supports the design, structuring, and delivery of client reports and presentations that are appropriate to the characteristics or needs of the audience.</li><li>
Act as primary contact for clients on a project; may also deliver some findings to clients.</li><li>
Recommends improvements and alternative solutions to resolve problems on projects to address client needs.</li><li>
May identify new business opportunities of follow-on work and new leads at assigned client.</li><li>
Provides follow-up with client after project deliverable has been completed to ensure client satisfaction.</li><li>
Proactively develops broader and deeper knowledge of related consulting and life sciences research methodologies through on-the-job experience and participation in training and mentorship opportunities.</li><li>
Begins to develop specific subject matter expertise to support Centers of Excellence or other specialty groups within PCS.</li><li>
When acting as Project Manager, proactively manages project timelines, project finances, and manages day-to-day communication with the client and team members.</li></ul><div><b>
Qualifications</b>:</div><ul><li><b>
Educational and Professional Experience:
</b><ul><li><b>Master&rsquo;s or doctorate degree in the social sciences or life sciences.</b></li><li><b>
5&ndash;8 years of consulting experience managing and delivering COA (mainly PRO) selection, creation, and validation projects for pharmaceutical or life sciences clients.</b></li></ul></li><li><b>
Professional Skills:</b> Solid project management skills and client relationship building skills. Works willingly and effectively with others in and across the organization to accomplish team goals. Ability to manage multiple projects, juggle priorities, and deliver on tight deadlines. Knowledge of key issues and current developments in the life science industry, particularly around qualitative and mixed-methods approaches to COA development and validation. Excellent presentation and communication skills. Some subject matter expertise to effectively manage projects.</li><li><b>
Technical Skills: </b>Experience in qualitative research methods and literature review methods required. Additional survey research and mixed-methods or quantitative research methods experience preferred. Proficient in MS Office (Word, Excel, PowerPoint); experience with bibliographic software, such as Zotero; experience with qualitative coding software, such as MAXQDA.</li><li><b>
Language and Travel: </b>Fluency in English and no travel requirements (with occasional travel for conferences or client meetings possible).</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role, when annualized, is $95,300.00 - $237,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

Manager, Patient-Centered Research

<div><div><div>Durham, United States of America | Full time | Home-based | R1530148</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><b><br>
About the Team:</b></div><div>
At IQVIA, our Patient Centered Solutions (PCS) team is dedicated to integrating the patient voice into medical research and development. Our scientific consulting services group conducts qualitative, quantitative, and mixed methods studies to better understand the patient, clinician, or caregiver experience.</div><div>
Projects range in size, type, and across multiple disease areas, and include clinical outcome assessment (COA) development, modification, and validation to support medical product development; strategic consulting for regulatory needs; exploratory analyses of existing data; literature review and gap analysis; and non-interventional studies with conceptualization, primary data collection via qualitative and/or quantitative methods, analysis, interpretation/synthesis, and dissemination phases. You'll enjoy a rewarding career in a collaborative, multicultural environment that values growth and development.</div><div><b>
Role Overview</b>:</div><div>
Join IQVIA as a Manager and play a key role in executing and delivering on primary literature reviews, data collection efforts, and analysis/reporting of qualitative and/or quantitative data. Your expertise will support customers in life science and population health markets with patient reported outcome (PRO) and other COA solutions, and will directly influence the success of clinical trials and patient-centered, observational studies. In this role, you will be responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. You will also identify and elevate potential new business opportunities and assist in the business development and proposal process. You will also receive the training, mentorship, and additional experience needed to advance in a research career track.</div><div><b>
Key Responsibilities</b>:</div><ul><li>
Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects, leveraging primarily qualitative or mixed-methods approaches.</li><li>
Reviews and analyzes client requirements or problems and assists in the development of proposals of cost-effective solutions that ensure profitability and high client satisfaction.</li><li>
Provides direction and guidance to Consultants, and where relevant, to Statistical Services assigned to engagement on overall project objectives, client needs, and scientific execution of the project with assistance from subject matter experts (SMEs).</li><li>
Develops or oversees development of detailed documentation and specifications, including protocol and study document development.</li><li>
Performs or oversees qualitative analyses to assist in the reporting of studies to address client needs and the development of client specific solutions.</li><li>
Supports the design, structuring, and delivery of client reports and presentations that are appropriate to the characteristics or needs of the audience.</li><li>
Act as primary contact for clients on a project; may also deliver some findings to clients.</li><li>
Recommends improvements and alternative solutions to resolve problems on projects to address client needs.</li><li>
May identify new business opportunities of follow-on work and new leads at assigned client.</li><li>
Provides follow-up with client after project deliverable has been completed to ensure client satisfaction.</li><li>
Proactively develops broader and deeper knowledge of related consulting and life sciences research methodologies through on-the-job experience and participation in training and mentorship opportunities.</li><li>
Begins to develop specific subject matter expertise to support Centers of Excellence or other specialty groups within PCS.</li><li>
When acting as Project Manager, proactively manages project timelines, project finances, and manages day-to-day communication with the client and team members.</li></ul><div><b>
Qualifications</b>:</div><ul><li><b>
Educational and Professional Experience:
</b><ul><li><b>Master&rsquo;s or doctorate degree in the social sciences or life sciences.</b></li><li><b>
5&ndash;8 years of consulting experience managing and delivering COA (mainly PRO) selection, creation, and validation projects for pharmaceutical or life sciences clients.</b></li></ul></li><li><b>
Professional Skills:</b> Solid project management skills and client relationship building skills. Works willingly and effectively with others in and across the organization to accomplish team goals. Ability to manage multiple projects, juggle priorities, and deliver on tight deadlines. Knowledge of key issues and current developments in the life science industry, particularly around qualitative and mixed-methods approaches to COA development and validation. Excellent presentation and communication skills. Some subject matter expertise to effectively manage projects.</li><li><b>
Technical Skills: </b>Experience in qualitative research methods and literature review methods required. Additional survey research and mixed-methods or quantitative research methods experience preferred. Proficient in MS Office (Word, Excel, PowerPoint); experience with bibliographic software, such as Zotero; experience with qualitative coding software, such as MAXQDA.</li><li><b>
Language and Travel: </b>Fluency in English and no travel requirements (with occasional travel for conferences or client meetings possible).</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role, when annualized, is $95,300.00 - $237,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

<div><div><div>Valencia, United States of America | Full time | Office-based | R1518990</div></div><p></p><div><div><br>
We are seekinga <b>Laboratory Associate- Flow Cytometry </b>to join IQVIA&rsquo;s laboratory business at Valencia, CA.</div><div><b>
Shift: Tuesday to Saturday 4PM to 12:30 AM
</b></div><div>We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.</div><h2 class="jobSectionHeader"><b>
What you&rsquo;ll be doing:</b></h2><ul><li>Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines.</li><li>Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.</li><li>Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.</li><li>Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.</li><li>Assists in quality investigations, deviations, and resolution.</li><li>Prepares buffers and solutions for analysis, as required.</li><li>Assists in the review and update of laboratory procedures and techniques.</li><li>Guides entry level staff on routine procedures and supports on-boarding of new staff.</li><li>Performs and document calibration and maintenance of laboratory equipment as assigned.</li><li>Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.</li><li>Assists in the review and development of laboratory procedures and techniques.</li><li>Assists in the implementation of procedural changes as assigned.</li><li>Notifies inventory staff of supply shortages.</li><li>May represent lab team on cross functional projects.</li><li>Responsible for clear, accurate, and timely communications with cross functional stakeholders.</li><li>Participates in continuing education through self-study, attending training sessions and lectures and meetings.</li><li>Supports safety, quality, and 6S requirements and initiatives.</li><li>Complies with company's procedures and applicable regulatory requirements.</li></ul><h2 class="jobSectionHeader"><b>
The Knowledge, Skills and Abilities needed for this role:</b></h2><ul><li><div>
Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science,<br>
medical laboratory technology or cytotechnology.) Req</div></li></ul><ul><li>6 months experience in a regulated laboratory environment. Pref</li><li>Requires basic knowledge of assigned technical area, systems and procedures obtained through prior work experience.</li><li>Demonstrates understanding of functional area and responsibilities.</li><li>Working knowledge of any applicable regulatory standards within area of responsibility, such as Good Laboratory Practices (GLP).</li><li>Proficiency with relevant laboratory techniques.</li><li>Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.</li><li>Experience working with automation or specialized laboratory equipment.</li><li>Proficiency with routine and some non-routine laboratory calculations regarding batches and specimens including averages, means, standard deviations, and various quality control metrics.</li><li>Good computer skills using Microsoft Outlook, Word and Excel.</li><li>Capable of handling multiple tasks simultaneously.</li><li>Strong attention to detail and accuracy.</li><li>Ability to effectively collaborate with internal stakeholders.</li></ul><h2 class="jobSectionHeader"><b>
What We Offer You:</b></h2><div>
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&rsquo; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</div><div>
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.</div><div>
If you&rsquo;re looking to unleash your potential, join IQVIA&rsquo;s laboratory business, to help make the extraordinary possible!</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><div>
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. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role, when annualized, is $34,700.00 - $72,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.</div></div><div></div>

Lab Associate - Flow Cytometry

Join IQVIA and explore 59   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.

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