clinical audiologist

Aga Khan Health Services

<div><div><div><div><b>Posted date</b></div> <div>24th December, 2025</div> <div><b>Last date to apply</b></div> <div>31st December, 2025</div>
</div><br>
<div><div><b>Country</b></div> <div>Pakistan</div> <div><b>Locations</b></div> <div>Gilgit, Gilgit Baltistan, Pakistan</div>
</div><br>
<div><div><b>Category</b></div> <div>Health Care
</div></div><br>
<div><div><b>Type</b></div> <div>Full Time</div> <div><b>Position</b></div> <div>1</div>
</div><br>
<div><div><b>Experience</b></div> <div>1 years</div></div></div></div>
<br><p></p><div><p><b>Background:</b> Aga Khan Health Service, Pakistan (AKHS, P) runs one of the largest not-for-profit private healthcare systems in the country, with a focus on the regions of Gilgit-Baltistan, Khyber-Pakhtunkhwa, Punjab, and Sindh. Its core focus includes initiatives for hard-to-reach populations through services like outreach clinics, training of community midwives to provide low-cost health services in remote areas, screening for non-communicable diseases, and digital health solutions.</p>
<p><b>
Position Summary: </b>Aga Khan Health Service, Pakistan is looking for a competent <b>Audiologist </b>base at<b> Aga Khan Diagnostic Centre, Jutial Gilgit</b>.</p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Conduct hearing assessments including audiometry, tympanometry, and other diagnostic tests.</li>
<li>Diagnose hearing loss and balance disorders.</li>
<li>Recommend and fit hearing aids and assistive listening devices.</li>
<li>Provide counseling and rehabilitation services to patients and families.</li>
<li>Maintain accurate patient records and reports.</li>
<li>Ensure infection control practices and equipment maintenance.</li>
<li>Participate in community awareness programs and hearing screening camps.</li>
<li>Collaborate with ENT specialists, physicians, and rehabilitation teams.</li>
<li>Follow AKHSP policies, medical protocols, and ethical standards.</li>
<li>Contribute to quality improvement initiatives.</li>
</ul>
<p><b>Qualifications &amp; Experience:</b></p>
<ul>
<li>Bachelor&rsquo;s or master&rsquo;s degree in Audiology.</li>
<li>1 year relevant experience</li>
<li>Strong clinical and diagnostic skills.</li>
<li>Excellent communication and counseling skills.</li>
<li>Ability to work in a multidisciplinary team.</li>
<li>Patient-centered approach.</li>
<li>Documentation and reporting skills.</li>
<li>Basic computer literacy.</li>
</ul>
<p><b><i>Only shortlisted candidates will be called for test/interview. AKHS, P is an equal opportunity employer and females are encouraged to apply.&rdquo;</i></b></p>
<p><b><i>
Considering the urgency of positions, interviews will be conducted on rolling basis</i></b></p>
<p>
AKHS is committed to reducing our impact on climate and the environment and have set ourselves the goal of striving for net-zero carbon operations by 2030. All staff is expected to take part in making this a reality. The <b>Audiologist </b>accompanied with his/her Line Manager is expected to identify and understand which aspects of his/her work have most impact on the environment, and define tasks, work, and personal goals within his/her work plan to reduce these impacts and bring AKHS closer to net zero.</p>
<p>
Interested candidates meeting the criteria can apply latest by <b>December 31, 2025</b></p></div><p></p>

Audiologist

University Hospital Sharjah

<div></div><div><p><b>Date: </b>24 Dec 2025
</p><p><b>Location:</b> Sharjah, AE
</p><p><b>Company: </b>University Hospital Sharjah
</p><div><div><div><div><h2 class="jobSectionHeader"><b>Position Summary</b></h2>
</div><div><p>
Responsible to work in Audiology Clinic in close relation with ENT, Paediatric, Neonatology departments by doing the hearing evaluation for infants and children, hearing and balance evaluation of adults and geriatric population and if required hearing aid trial/ fitting, cochlear implant mapping/ counselling.</p>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Summary of Main Duties</b></h2>
</div><div><ul><li>Actively participates in upholding and promoting the vision and culture of University Hospital &ndash; Sharjah (UHS)</li></ul>
<ul><li>Performs diagnostic evaluations of the patients hearing abilities and vestibular function, conferred with appropriate professionals regarding patient care and management, initiated appropriate rehabilitative services.</li></ul>
<ul><li>Conducts Universal Neonatal hearing screening program at UHS including, OAE&rsquo;s and AABR.</li><li>Performing NRT while doing CI surgery.</li><li>Perform Cochlear Implant Mapping and Monitor the CI outcome in children and adults</li></ul>
<ul><li>Perform hearing aids trial and fitting for children, adults and geriatric patients with hearing loss. by doing aided audiogram, REM, and programming of hearing aids</li></ul>
<ul><li>Perform diagnostic vestibular evaluation for children, adults and geriatric population when required and initiate the vestibular rehabilitation process.</li></ul>
<ul><li>Counsels patients with hearing loss regarding their type and degree of hearing loss and possible rehabilitation methods, benefits and limitations of hearing aids, hearing aid technology, patients candidacy for hearing aids, cochlear implants etc,</li></ul>
<ul><li>Responsible and in charge for the Audiology Unit</li></ul>
<ul><li>Measures hearing acuity and vestibular assessment of patients of all ages, using Pure Tone Audiometry, Immittance Audiometry, Behavioral Observation Audiometry, Electrocochleography (EcohG), Auditory Brainstem response Audiometry (ABR), Late Latency Response (LLR), Auditory Steady State Response (ASSR), Speech Evoked ABR, Vestibular Evoked Myogenic Potential (VEMP), Video Head Impusle test(vHIT), Video Nystagmography, Rotary chair tests etc.</li></ul>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Responsibilities</b></h2>
</div><div><ul><li>Performs differential diagnosis of patients with cochlear ,vestibular, retro cochlear, Auditory neuropathy and central auditory processing deficits by performing tests like SPIN, ,High and Low rate ABR, VEMP, ARLT and CAPD tests</li></ul>
<ul><li>Conducts CME for Medical Professionals and Allied health professionals.</li></ul>
<ul><li>In-charge for all the equipment&rsquo;s in the Audiology clinic</li></ul>
<ul><li>Responsible for coordinating the cochlear implant program at UHS</li></ul>
<ul><li>Participates in all aspects of the International Accreditation program to assist UHS attain and maintain international accreditation standards</li></ul>
<ul><li>Self Professional Development: Participate in internal orientation (mandatory), internal ongoing Continual Medical Education programs (CME), attend external conferences, workshops, seminars and courses that will enhance and maintain a current knowledge base.</li></ul>
<ul><li>Provide clinical teaching to the students when and where required from the UOS</li></ul>
<ul><li>The employment terms and conditions for this position are specified in the individuals Employment Contract</li></ul>
<ul><li>Will retain all necessary registration/license requirements</li></ul>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Position Requirements/Qualifications</b></h2>
</div><div><p><b>
Position</b><br>
<b>Requirements/Qualifications</b>
</p><ul><li><b>Mandatory: </b>Master&rsquo;s Degree in Audiology/Speech &amp; Hearing
 </li></ul><p><b>Desirable:</b> Doctor of Audiology (AuD)/PhD</p>
<p><b>Licenses/Registration</b>
</p><ul><li>Must have a valid UAE MOH Evaluation</li></ul>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Position criteria Other Skills/Abilities</b></h2>
</div><div><p><b>
Position criteria</b></p>
<ul><li>Senior Audiologist.</li></ul>
<ul><li>Minimum 7 years&rsquo; experience as Senior Audiologist at Hospital settings</li></ul>
<p><b>Other Skills/Abilities</b>
</p><ul><li>Maintains the audiology clinic equipment&rsquo;s with high technical efforts, daily calibration, assists in routine internal calibration by maintaining up-to-date quality control and/or quality assurance records.</li><li>Operational skills for all audiology equipment&rsquo;s</li></ul></div></div></div></div></div><p></p>

Senior Audiologist

The IMA Group

<div><div><h2 class="jobSectionHeader"><b>Clinical Research Coordinator &ndash; Austin, TX</b></h2><div>
(<b>Clinical Research - Research Coordinator - Research Assistant - Clinical Research Associate</b>)</div><div>
</div><div>
Join <b>IMA Clinical Research</b> as a <b>Clinical Research Coordinator</b> and help drive innovative <b>clinical research</b> studies that improve patient outcomes. This role is ideal for candidates experienced in <b>Research</b>, <b>Research Coordination</b>, <b>Clinical Research Associate</b> work, or <b>Research Assistant</b> responsibilities.</div><h3 class="jobSectionHeader"><b>
What You&rsquo;ll Do</b></h3></div><ul><li>
Support and coordinate clinical research trials from start to finish</li><li>
Guide patients through study visits and research procedures</li><li>
Work closely with investigators, sponsors, labs, and monitors</li><li>
Complete blood draws and clinical tasks</li><li>
Maintain accurate research documentation (ALCOA)</li></ul><div><h3 class="jobSectionHeader"><b>
What We&rsquo;re Looking For</b></h3></div><ul><li>
At least 2 years of <b>clinical research</b> experience (required)</li><li>
Phlebotomy experience (required)</li><li>
Bachelor&rsquo;s degree; Master&rsquo;s or CCRC a plus</li><li>
Strong organization skills and ability to manage multiple research studies</li></ul><div><h3 class="jobSectionHeader"><b>
What We Offer</b></h3></div><ul><li>
Fast-paced clinical research environment</li><li>
No on-call work</li><li>
Tuition support &amp; student loan assistance</li><li>
Medical, dental, vision, 401(k) match, PTO, holidays</li></ul><div><div>
</div><div>
Join our growing <b>Clinical Research</b> team and build your career as a <b>Clinical Research Coordinator</b>, <b>Research Coordinator</b>, <b>Clinical Research Associate</b>, or <b>Research Assistant</b>.</div></div><div>
</div><div></div><div><b><i>The IMA Group is an Affirmative Action/Equal Opportunity Employer</i></b>
</div><div></div><div>Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
</div><div></div><div>#LI-EG1 #LI-ONSITE</div></div>

Clinical Research Coordinator - Growing Clinical Research Team - Austin, TX

Beacon Hill

<div>
 <p>
  <strong>
   What You&rsquo;ll Do
  </strong>
 </p>
 <p>
  In this role, you will contribute to the clinical development of early‑stage oncology programs and support studies across multiple phases. Responsibilities may include, but are not limited to:
 </p>
 <ul>
  <li>
   Developing clinical development concepts and plans in collaboration with clinical leadership, with an emphasis on early oncology assets.
  </li>
  <li>
   Drafting protocol synopses, full study protocols, and protocol amendments.
  </li>
  <li>
   Preparing and reviewing informed consent forms and evaluating site‑specific ICF submissions.
  </li>
  <li>
   Partnering with Clinical Operations on site selection, study start‑up, and ongoing communication.
  </li>
  <li>
   Contributing to the creation and maintenance of clinical sections of investigator brochures, including coordinating initial versions and annual updates.
  </li>
  <li>
   Writing and/or reviewing clinical and safety content for regulatory submissions (e.g., global marketing applications).
  </li>
  <li>
   Representing clinical/medical perspectives on study teams and supporting clinical leadership in strategic decision‑making.
  </li>
  <li>
   Participating in clinical sub‑team activities.
  </li>
  <li>
   Reviewing safety data, data listings, and serious adverse event information to support ongoing study evaluation.
  </li>
  <li>
   Contributing to or leading the authorship of clinical study reports and publications.
  </li>
  <li>
   Creating study‑ or program‑related presentation materials for internal and external audiences.
  </li>
  <li>
   Providing training to internal teams, CRO partners, and study site personnel on therapeutic area topics, program background, and study protocols.
  </li>
  <li>
   Supporting and participating in advisory boards and expert consultations.
  </li>
  <li>
   Conducting therapeutic area research, competitive landscape assessments, and indication‑specific analyses.
  </li>
  <li>
   Establishing and maintaining relationships with key investigators and thought leaders.
  </li>
  <li>
   Supporting interactions with global health authorities, including preparing responses to inspection findings and audit observations.
  </li>
  <li>
   Assisting with regulatory updates and submission‑related clinical deliverables.
  </li>
  <li>
   Supporting medical monitoring activities for Phase 2 or 3 clinical trials, ensuring patient safety and contributing guidance across study design, execution, and reporting.
  </li>
 </ul>
 <p>
  Additional contributions may include presenting study outcomes to internal committees, external scientific groups, or advisory bodies; contributing to scientific congress presentations; and supporting publication activities. Program‑level responsibilities may involve authoring or reviewing clinical summaries, overviews, risk management materials, periodic safety updates, and labeling sections.
 </p>
 <p>
  <strong>
   Requirements
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree with substantial clinical oncology expertise gained through prior clinical development experience.
  </li>
  <li>
   Advanced degree or clinical qualification in oncology (e.g., Master&rsquo;s, MD, PharmD, PhD, or equivalent) preferred.
  </li>
  <li>
   Minimum of 4 years of industry experience in oncology drug development.
  </li>
  <li>
   Prior involvement in clinical development programs, ideally across all study phases from initiation through reporting.
  </li>
  <li>
   Experience working with small‑molecule oncology therapeutics is advantageous.
  </li>
  <li>
   Strong competency in protocol design, clinical data interpretation, and medical monitoring.
  </li>
  <li>
   Experience evaluating safety data and adverse events in therapeutic trials is preferred.
  </li>
  <li>
   Solid understanding of Good Clinical Practice (GCP) and regulatory expectations.
  </li>
  <li>
   Excellent written and verbal communication skills.
  </li>
  <li>
   Ability to work effectively in a fast‑paced, evolving environment
  </li>
 </ul>
</div>


Clinical Scientist Director

IQVIA

<div><div><div>Abington Township, United States of America | Full time | Home-based | R1520965</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><i><br>
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</i></div><div>
Job Overview<br>
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times.<br>
<br>
Essential Functions<br>
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul><br>
Qualifications<br>
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></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>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. 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>

Clinical Trial Manager I, IQVIA Biotech

<div><div><div>New City, United States of America | Full time | Home-based | R1520965</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><i><br>
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</i></div><div>
Job Overview<br>
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times.<br>
<br>
Essential Functions<br>
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul><br>
Qualifications<br>
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></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>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. 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>Berkeley, United States of America | Full time | Home-based | R1520965</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><i><br>
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</i></div><div>
Job Overview<br>
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times.<br>
<br>
Essential Functions<br>
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul><br>
Qualifications<br>
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></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>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. 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>

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