accounting operations associate Jobs in Karachi Pakistan

accounting operations associate

clinical trials quality assurance associate (night) Jobs in Karachi Pakistan

clinical trials quality assurance associate (night)

software quality assurance engineer Jobs in Karachi Pakistan

software quality assurance engineer

sqa automation analyst Jobs in Karachi Pakistan

sqa automation analyst

us patient enrollment coordinator (evening shift) Jobs in Karachi Pakistan

us patient enrollment coordinator (evening shift)

clinical trials quality assurance associate night

Minerva Research Solutions

<div>
 <strong>
  JOB DESCRIPTION:
  <br/>
  <br/>
 </strong>
 Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
 <br/>
 <br/>
 Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.
 <br/>
 <br/>
 We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
 <br/>
 <br/>
 Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
 <br/>
 <br/>
 <strong>
  Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness
  </li>
  <li>
   Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations
  </li>
  <li>
   Perform quality control checks; identify and track source documentation errors and non-conformances with requirements
  </li>
  <li>
   Provide ongoing compliance support including but not limited to:
  </li>
  <li>
   Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans
  </li>
  <li>
   Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs)
  </li>
  <li>
   Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities
  </li>
  <li>
   Assist in preparing for all Sponsor and FDA audits
  </li>
  <li>
   Assist in conducting internal audits to review key processes
  </li>
  <li>
   Provide appropriate support to assigned cross-functional workgroups
  </li>
  <li>
   Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement
  </li>
  <li>
   Query resolution and data entry and questionnaire preparation regarding the respective studies
  </li>
  <li>
   Other related Quality Assurance projects as assigned
  </li>
  <li>
   The QA Associate will report to the Quality Assurance Lead
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Knowledge, Education, and Experience:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply
  </li>
  <li>
   In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials
  </li>
  <li>
   Knowledge of IRB requirements
  </li>
  <li>
   1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred.
  </li>
  <li>
   Experience including external clinical/regulatory and document auditing will be a plus
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills and Abilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Good communication skills (interpersonal, written, verbal)
  </li>
  <li>
   Strong attention to detail and good time management skills
  </li>
  <li>
   Flexible attitude concerning work assignments
  </li>
  <li>
   Ability to manage multiple and varied tasks in a fast-moving environment
  </li>
  <li>
   Ability to interact professionally at all levels within the organization
  </li>
  <li>
   Knowledge of the HIPAA Privacy Act and its application to clinical research
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive salary and performance-based bonuses
  </li>
  <li>
   Medical health insurance coverage
  </li>
  <li>
   Employees Old-age benefits coverage
  </li>
  <li>
   Flexible work hours and remote work options
  </li>
  <li>
   Professional learning and development support
  </li>
  <li>
   Generous vacation and paid time off
  </li>
  <li>
   Employee assistance programs for mental health
  </li>
  <li>
   Company-sponsored events and team-building activities
  </li>
  <li>
   Diverse, professional, and inclusive work environment
  </li>
  <li>
   Opportunities for career growth
  </li>
  <li>
   Cutting-edge technology and tools
  </li>
  <li>
   Family-friendly policies, including parental leave
  </li>
  <li>
   Commuter benefits or transportation assistance
  </li>
  <li>
   Social responsibility and community involvement programs
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Openings:
  <br/>
  <br/>
 </strong>
 04 positions
 <br/>
 <br/>
 Full-time
 <br/>
 <br/>
 On-site job
 <br/>
 <br/>
 <strong>
  Work Schedule Timings:
  <br/>
  <br/>
 </strong>
 Monday to Friday
 <br/>
 <br/>
 Evening Shift (07 PM to 03 AM)
 <br/>
 <br/>
 (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 <br/>
 <br/>
 Powered by JazzHR
 <br/>
 <br/>
 RlJhA3EJD3
</div>


Clinical Trials Quality Assurance Associate (Night)

<div><p><b>JOB DESCRIPTION:</b><br>
<br>
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.</p><p>
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.<br>
<br>
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.<br>
<br>
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.</p><p><b>
Responsibilities:</b></p><ul><li>
Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.</li><li>
Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.</li><li>
Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.</li><li>
Provide ongoing compliance support including but not limited to:</li><li>
Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.</li><li>
Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).</li><li>
Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.</li><li>
Assist in preparing for all Sponsor and FDA audits.</li><li>
Assist in conducting internal audits to review key processes.</li><li>
Provide appropriate support to assigned cross-functional workgroups.</li><li>
Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.</li><li>
Query resolution and data entry and questionnaire preparation regarding the respective studies.</li><li>
Other related Quality Assurance projects as assigned.</li><li>
The QA Associate will report to the Quality Assurance Lead</li></ul><p><b>
Knowledge, Education, and Experience:</b></p><ul><li>
Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply.</li><li>
In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.</li><li>
Knowledge of IRB requirements.</li><li>
1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred..</li><li>
Experience including external clinical/regulatory and document auditing will be a plus</li></ul><p><b>
Skills and Abilities:</b></p><ul><li>
Good communication skills (interpersonal, written, verbal)</li><li>
Strong attention to detail and good time management skills</li><li>
Flexible attitude concerning work assignments</li><li>
Ability to manage multiple and varied tasks in a fast-moving environment</li><li>
Ability to interact professionally at all levels within the organization.</li><li>
Knowledge of the HIPAA Privacy Act and its application to clinical research.</li></ul><b>
Benefits:</b><ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Flexible work hours and remote work options.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional, and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul><b>
Openings:</b><p>
04 positions<br>
Full-time<br>
On-site job<br>
<br>
<b>Work Schedule Timings:</b><br>
Monday to Friday<br>
Evening Shift (07 PM to 03 AM)<br>
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)</p><p>
</p><p>RlJhA3EJD3</p></div>

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
 <br/>
 <br/>
 Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.
 <br/>
 <br/>
 We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
 <br/>
 <br/>
 Minerva Research Solution is looking for dynamic individuals in the role of Patient Enrollment Specialist responsible for screening new leads, conducting follow-ups, and documenting participants for assigned active clinical trials. This specialist contributes significantly to clinical trials by building a comprehensive database in the Clinical Trial Management System (CTMS) of willing and qualified study volunteers.
 <br/>
 <br/>
 <strong>
  Industry:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Information Technology &amp; Services
  </li>
  <li>
   Hospital &amp; Health Care
  </li>
  <li>
   Clinical-Trials and Research Industry
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct phone interviews and screenings for prospective clinical study participants in US
  </li>
  <li>
   Maintain an organized database of clinical study participants
  </li>
  <li>
   Develop outreach strategies to enhance participant recruitment
  </li>
  <li>
   Interact directly with study participants via phone calls, SMS, etc
  </li>
  <li>
   Collaborate with Medical Staff (CRCs) to ensure adequate subject recruitment for each study
  </li>
  <li>
   Enhance and maintain study documentation and volunteer records, including consent forms
  </li>
  <li>
   Assist in sales, marketing, and outreach efforts as needed
  </li>
  <li>
   Provide accurate study-related information to participants in US
  </li>
  <li>
   Cultivate a safe, positive, and fast-paced work environment
  </li>
  <li>
   Undertake other related duties and participate in special projects as assigned
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Behavioral Competencies:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conceptual capability, problem-solving, and decision-making ability
  </li>
  <li>
   Strong commitment to teamwork, work ethics, and etiquette
  </li>
  <li>
   Effective planning and organizing skills with priority setting
  </li>
  <li>
   Proactive knowledge and information sharing within the team
  </li>
  <li>
   Customer-focused with strong communication skills
  </li>
  <li>
   Active learning attitude with a continuous improvement mindset
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Qualifications:
  <br/>
  <br/>
 </strong>
 <strong>
  Essential:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s Degree in BDS, Pharm-D
  </li>
  <li>
   Good knowledge of Clinical Trials
  </li>
  <li>
   Computer literate with good knowledge of MS Office
  </li>
  <li>
   Proficiency in the English language written and spoken both.(MANDATORY)
  </li>
  <li>
   Therapeutic Communication in English with US accent is preferred
  </li>
  <li>
   6 months to 1 year experience in a relevant field
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive salary and performance-based bonuses
  </li>
  <li>
   Quarterly Bonus Structure
  </li>
  <li>
   Medical health insurance coverage for you and your family (Spouse &amp; Children)
  </li>
  <li>
   Employees Old-age benefits coverage
  </li>
  <li>
   40-hours Week
  </li>
  <li>
   Exposure to US Market
  </li>
  <li>
   Professional learning and development support
  </li>
  <li>
   Generous vacation and paid time off
  </li>
  <li>
   Employee assistance programs for mental health
  </li>
  <li>
   Company-sponsored events and team-building activities
  </li>
  <li>
   Diverse, professional and inclusive work environment
  </li>
  <li>
   Opportunities for career growth
  </li>
  <li>
   Cutting-edge technology and tools
  </li>
  <li>
   Family-friendly policies, including parental leave
  </li>
  <li>
   Commuter benefits or transportation assistance
  </li>
  <li>
   Social responsibility and community involvement programs
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Openings:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Equal opportunity employers
  </li>
  <li>
   Full-time
  </li>
  <li>
   On-site job (Night shift)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work Schedule Timings:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Monday to Friday
  </li>
  <li>
   7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
   <br/>
   <br/>
  </li>
 </ul>
 Powered by JazzHR
 <br/>
 <br/>
 25PToqYnDr
</div>


US Patient Enrollment Coordinator (Evening Shift)

<div><h2 class="jobSectionHeader"><b>Job description</b></h2><p>
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.</p><p>
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.<br>
<br>
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.<br>
<br>
Minerva Research Solution is looking for dynamic individuals in the role of Patient Enrollment Specialist responsible for screening new leads, conducting follow-ups, and documenting participants for assigned active clinical trials. This specialist contributes significantly to clinical trials by building a comprehensive database in the Clinical Trial Management System (CTMS) of willing and qualified study volunteers.</p><p><b>
Industry:</b></p><ul><li>
Information Technology &amp; Services</li><li>
Hospital &amp; Health Care</li><li>
Clinical-Trials and Research Industry</li></ul><p><b>
Key Responsibilities:</b></p><ul><li>
Conduct phone interviews and screenings for prospective clinical study participants in US.</li><li>
Maintain an organized database of clinical study participants.</li><li>
Develop outreach strategies to enhance participant recruitment.</li><li>
Interact directly with study participants via phone calls, SMS, etc.</li><li>
Collaborate with Medical Staff (CRCs) to ensure adequate subject recruitment for each study.</li><li>
Enhance and maintain study documentation and volunteer records, including consent forms.</li><li>
Assist in sales, marketing, and outreach efforts as needed.</li><li>
Provide accurate study-related information to participants in US.</li><li>
Cultivate a safe, positive, and fast-paced work environment.</li><li>
Undertake other related duties and participate in special projects as assigned.</li></ul><p><b>
Behavioral Competencies:</b></p><ul><li>
Conceptual capability, problem-solving, and decision-making ability.</li><li>
Strong commitment to teamwork, work ethics, and etiquette.</li><li>
Effective planning and organizing skills with priority setting.</li><li>
Proactive knowledge and information sharing within the team.</li><li>
Customer-focused with strong communication skills.</li><li>
Active learning attitude with a continuous improvement mindset.</li></ul><p><b>
Minimum Qualifications:</b></p><p><b>
Essential:</b></p><ul><li>
Bachelor&rsquo;s Degree in BDS, Pharm-D.</li><li>
Good knowledge of Clinical Trials.</li><li>
Computer literate with good knowledge of MS Office.</li><li><b><i>
Proficiency in the English language written and spoken both.(MANDATORY)</i></b></li><li>
Therapeutic Communication in English with US accent is preferred.</li><li>
6 months to 1 year experience in a relevant field.</li></ul><p><b>
Benefits:</b></p><ul><li>
Competitive salary and performance-based bonuses.</li><li>
Quarterly Bonus Structure.</li><li>
Medical health insurance coverage for you and your family (Spouse &amp; Children).</li><li>
Employees Old-age benefits coverage.</li><li>
40-hours Week.</li><li>
Exposure to US Market.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul><b>
Openings:</b><ul><li>
Equal opportunity employers</li><li>
Full-time</li><li>
On-site job <b>(Night shift)</b></li></ul><p><b><br>
Work Schedule Timings:</b></p><ul><li>
Monday to Friday</li><li>
7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)</li></ul><p>
</p><p>25PToqYnDr</p></div>

Aga Khan University

<div><div><div><div><div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>Introduction</b></h2></div>
<div><div>The Aga Khan University (AKU) is a pioneering institution of higher education with a mission to improve the quality of life in the developing world and beyond, through world-class teaching, research and healthcare delivery. AKU educates students for local and global leadership from campuses and teaching hospitals in six countries, primarily in Asia and East Africa. It generates new knowledge to solve challenges that affect billions of people, especially the most vulnerable. The University is a private, not-for-profit institution and part of the Aga Khan Development Network.</div><br>
<div></div>
<div>
The Centre for Regenerative Medicine (CRM) and Stem Cell Research is one of the most ambitious and mission-critical initiatives at AKU. Established in 2016, in collaboration with the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, University of California San Francisco (UCSF), the Centre is part of the Medical College in Pakistan. Integration with the research, clinical, and policy network of the Medical College enables access to, and engagement with, a broad intellectual network and interdisciplinary teams that include clinicians, basic scientists, students, health care leaders and decision makers. Engagement with Aga Khan University Hospital and its Clinical Trials Unit promotes clinical translation and priority-setting to enhance impact for patient benefit in the regions served by AKU.</div><br>
<div></div>
<div>
The Centre has pioneered research in regenerative medicine and stem cell biology in Pakistan. Its mission is to translate fundamental research on regionally relevant diseases into novel therapies. With existing infrastructure at the Centre and related labs, AKU is well-positioned to lead in regenerative and genomic medicine regionally, transforming healthcare by incorporating technologies like next-generation sequencing, gene editing, and cell-based interventions.</div><br>
<div></div>
<div>
The Centre comprises core research space for up to 28 bench researchers containing state-of the-art equipment, including a Fluorescence-activated Cell Sorter (FACS), confocal microscope, meta-system for chromosomal studies, a tissue regeneration laboratory with a bio-printer, three tissue culture facilities for induced Pluripotent Stem Cells (iPSC), primary patient sampling and quarantine, and an established cancer cell line laboratory.</div><br>
<div></div>
<div>
To fully realize the promise of the Centre and a bench-to-bedside approach, AKU is investing further in a state-of-the-art Translational Research Facility (TRF) with integrated animal research, genomics, gene editing, induced pluripotent stem cell iPSC and GMP-grade laboratories to bridge the gap between laboratory research and clinical applications, such as gene and cellular therapies.</div>
</div></div><div><div><h2 class="jobSectionHeader"><b>Responsibilities</b></h2></div>
<div><div>Reporting to the Dean of the Medical College, Pakistan, the Director, Centre for Regenerative Medicine and Stem Cell Research is responsible for strengthening regenerative medicine and genomic research across AKU by training fundamental, translational and clinical researchers and leading translational research programmes.</div><br>
<div></div>
<div><b>
The ideal candidate for the role:</b></div><div></div><div><br>
The Director will be an inspirational leader who can develop and implement a strategic vision for the Centre. They will promote a culture of learning, innovation, collaboration, teamwork, respect and ethical conduct of research. The Director will strengthen relationships with researchers and clinicians across AKU and build a network of local and global partners, inclusive of academia, government research facilities, and industry. The Director will be a leader in AKU&rsquo;s regions for policy development relative to regenerative and genomic medicine, ethics, commercialization opportunities, and community engagement.</div><br>
<div></div>
<div>
The ideal candidate will work in domains of regenerative and genomic medicine that align with regional priorities for South Asia and East Africa, including Mendelian and complex disorders. The high rates of consanguinity in Pakistan enables the discovery of novel pathogenic variants for Mendelian diseases. The Centre/AKU facilities enable the development of iPSC and animal models targeting patient-specific variants, precise gene editing, investigation of signaling pathways, and drug testing. Together, these activities provide functional validation of disease-causing variants and mechanisms and enable therapeutic development. Conditions with regional significance include blood disorders (sickle cell anaemia / thalassemia), neurodevelopmental disorders, metabolic disorders, cancers, and retinal disorders. The ideal candidate will have experience in bench-to-bedside translation of cell or gene therapies in these regionally relevant domains.</div><br>
<div></div>
<div>
This is a full-time position, with flexibility to consider a part-time arrangement for an exceptional candidate, in alignment with University policies.</div><br>
<div></div>
<div><b>
Specific responsibilities will include to:</b></div><br>
<div></div><ul>
<li>
lead interdisciplinary regenerative medicine research and training within the Medical College, Pakistan and AKU while strengthening local through international networks with a full range of stakeholders</li>
<li>leverage AKU assets, such as biobanks and longitudinal health outcomes and phenotype data for translational regenerative medicine research programmes</li>
<li>lead the development of cell and animal models to support foundational through translational research</li>
<li>develop strategies to build capacity for the clinical delivery of regenerative medicines, including cell and gene therapies by engaging Aga Khan University Hospital and its Clinical Trials Unit</li>
<li>ensure adequate space, capital and human resources are available to meet the research and manufacturing needs for clinical translation</li>
<li>ensure compliance with requirements of all regulatory and accrediting bodies;</li>
<li>articipate on external scientific and professional committees to enhance AKU&rsquo;s reputation in regenerative medicine</li>
<li>represent AKU at international conferences, symposia and other professional convenings; apply for national and international grants to sustain and enhance the Centre&rsquo;s strategic goals and research programmes.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements</b></h2></div>
<div><div><p>The ideal candidate will have:</p><br>
<p></p>
<ul>
<li>an MD, PhD, or an equivalent degree in a relevant discipline;</li>
<li>a minimum of 10 years relevant work experience, 5 years or more at the rank of Associate Professor and be eligible for appointment at AKU for the rank of Associate Professor or Professor;</li>
<li>a sustained and outstanding body of scholarship in translational regenerative medicine research, inclusive of cell or gene therapy development, as demonstrated through international peer-reviewed funding, publications, presentations, changes to practice or policy and/or other forms of dissemination that are recognized internationally;</li>
<li>a demonstrated record in faculty and staff mentorship and training of graduate students and postdoctoral/clinical fellows;</li>
<li>a demonstrated record of leadership of significant single or multi-site research programmes with high impact deliverables;</li>
<li>experience in working with legislators, community leaders, industry representatives, and philanthropic partners;</li>
<li>the ability to effectively represent the Centre in regional, national and international fora;</li>
<li>demonstrated commitment to promoting diversity, equity, inclusion and belonging;</li>
<li>demonstrated success in recruiting exceptional clinical and/or bench scientists.</li></ul><br>
<p></p>
</div>
</div></div><div><div><h2 class="jobSectionHeader"><b>To Apply</b></h2></div>
<div><div><p>Interested candidates are requested to submit their applications addressed to The Senior Manager, Talent Acquisition via email hr.recruitment@aku.edu with the position title <b>Director, Centre for Regenerative Medicine and Stem Cell Research</b> in the subject line. Applications should include:</p>
<ul>
<li>A covering letter expressing interest and suitability for the role;</li>
<li>An up-to-date Curriculum Vitae;</li>
<li>Names and contact details of three referees (referees will only be approached at the final stage of the search and selection process, and only with the candidate&rsquo;s express permission).</li>
</ul>
<p>No hard copy applications will be accepted. Only shortlisted candidates will be contacted.</p>
<p>
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.</p>
<p>
Comprehensive employment reference checks for the finalists will be conducted.</p>
</div><p>
Applications should be submitted latest by <b>January 31, 2026</b></p></div></div></div></div></div></div></div></div></div></div></div><div></div>

Director, Centre for Regenerative Medicine and Stem Cell Research

NCCI

<p><b>Job Opportunity &mdash; Lady Medical Officer (L.M.O.)</b></p><p><b>Neurospinal &amp; Cancer Care Institute (NCCI), Karachi</b><br/>invites applications for the position of <b>Lady Medical Officer</b> to support our clinical services.</p><p><b>Position:</b> Lady Medical Officer (L.M.O.)</p><p><b>Duty Timings:</b></p><ul><li><b>Evening Shift:</b> 2:00 PM to 8:00 PM</li><li><b>Alternate Night Shift:</b> 8:00 PM to 8:00 AM</li></ul><p><b>Gender:</b> only Female</p><p><b>Location:</b> NCCI Hospital, Saddar, Karachi</p><p><b>Key Responsibilities:</b></p><ul><li>Monitor admitted patients &amp; maintain clinical notes</li><li>Coordinate with consultants for patient management</li><li>Attend emergency calls &amp; provide immediate care</li><li>Ensure smooth functioning of ward services during duty hours</li><li>Maintain documentation, prescriptions &amp; follow-up instructions</li></ul><p><b>Eligibility Criteria:</b></p><ul><li>MBBS from a recognized institution, FCPS part-I cleared.</li><li>Valid PMC registration</li><li>Must be experience of ICU, Emergency, ward and Preference will be given to Peads &amp; Gyne departments.</li><li>Strong clinical judgement &amp; patient handling skills</li><li>Willingness to work in evening + alternate night rotation</li></ul><p><b>We Offer:</b></p><ul><li>Competitive salary</li><li>Supportive work environment</li><li>Learning &amp; career advancement opportunities</li></ul><p><b>How to Apply</b></p><p>Interested candidates may submit their CV at:</p><p><b>hr@ncci.org.pk</b><br/>or submit directly to <b>HR Department, NCCI Hospital, Saddar, Karachi</b></p><p>Job Type: Full-time</p><p>Pay: Rs90,000.00 - Rs100,000.00 per month</p><p>Work Location: In person</p>

Lady Medical Officer

<div><p><b>Location:</b> Karachi (On-site)<br>
<b>Department:</b> Patient Experience &amp; Support<br>
<b>Employment Type:</b> Full-Time | Night Shift</p><p></p><h3 class="jobSectionHeader"><b>
Who We Are</b></h3><p>
Minerva Research Solutions is a leading Clinical Trial Management and Support organization dedicated to elevating global healthcare outcomes through innovation, operational excellence, and uncompromising quality. We partner with biotech, pharmaceutical, and healthcare institutions to deliver integrated services across the clinical trial value chain &mdash; from feasibility to closeout.</p><p>
Our portfolio spans <b>Data Operations, Patient Recruitment, and Regulatory Services</b>, enabling clients to accelerate the development of breakthrough therapies with accuracy, agility, and regulatory confidence. Governed by <b>FDA</b> and <b>ICH-GCP</b> standards, we are committed to delivering data integrity, participant safety, and reliable insights at every touchpoint.</p><p>
We are expanding our Customer Experience function and seeking a <b>customer-centric, articulate, and resilient professional</b> to join our high-performance team.</p><p></p><h3 class="jobSectionHeader"><b>
Role Summary</b></h3><p>
As a Call Center Representative, you will serve as the frontline ambassador for Minerva, representing our service standards, values, and commitment to excellence. You will play a critical role in guiding patients, partners, and stakeholders with accurate information and empathetic engagement, ensuring a seamless and compliant service experience.</p><p></p><h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><ul><li><p>
Manage inbound and outbound interactions to support patient and client inquiries on clinical services, ensuring clarity, professionalism, and accuracy.</p></li><li><p>
Deliver a frictionless customer journey by proactively understanding needs, resolving concerns, and providing tailored support.</p></li><li><p>
Support appointment coordination, participant onboarding, and dissemination of study-related information, ensuring compliance with confidentiality and data-handling standards.</p></li><li><p>
Maintain a high standard of service delivery aligned with Minerva&rsquo;s CX principles and regulatory guidelines (FDA/ICH-GCP).</p></li><li><p>
Collaborate with cross-functional teams to drive timely issue resolution and consistent service continuity.</p></li><li><p>
Maintain complete and compliant CRM documentation of all customer interactions.</p></li><li><p>
Identify service gaps and escalate complex situations to the relevant teams for swift resolution.</p></li></ul><p></p><h3 class="jobSectionHeader"><b>
Required Qualifications &amp; Experience</b></h3><ul><li><p>
Bachelor&rsquo;s degree in any discipline (or equivalent).</p></li><li><p><b>
Exceptional communication skills in English &mdash; neutral/US accent preferred.(MANDATORY)</b></p></li><li><p>
Minimum <b>1 year of international customer support experience</b> (contact center, BPO, or shared services).</p></li><li><p>
Experience in healthcare, life sciences, or clinical research is a plus but not mandatory.</p></li><li><p>
Strong analytical thinking, emotional intelligence, and client-service orientation.</p></li><li><p>
Ability to perform in a target-driven, high-volume, and fast-paced environment.</p></li><li><p>
Proficiency in customer service platforms/CRM tools and MS Office applications.</p></li><li><p>
Willingness to work night shifts and adjust to evolving business needs.</p></li></ul><p></p><h3 class="jobSectionHeader"><b>
What You&rsquo;ll Gain at Minerva</b></h3><ul><li><p>
Competitive compensation with performance-based rewards</p></li><li><p>
Comprehensive medical insurance</p></li><li><p>
EOBI retirement benefits</p></li><li><p>
Structured Learning &amp; Development pathways, including certifications and career mobility</p></li><li><p>
Paid annual, medical, and casual leave</p></li><li><p>
Mental well-being and employee support programs</p></li><li><p>
Inclusive, collaborative, and growth-driven work culture</p></li><li><p>
Internal recognition &amp; employee engagement initiatives</p></li><li><p>
Modern digital tools and a technology-forward workplace</p></li><li><p>
Transportation facility for female staff &amp; conveyance allowance for male staff</p></li><li><p>
Night shift allowance</p></li><li><p>
Family-supportive policies, including parental leave</p></li><li><p>
Opportunities to contribute to community and social impact programs</p></li></ul><p></p><h3 class="jobSectionHeader"><b>
Work Schedule</b></h3><p><b>
Monday &ndash; Friday</b><br>
<b> 7:00 PM &ndash; 3:00 AM (On-site)</b></p><p></p><h3 class="jobSectionHeader"><b>
Diversity, Equity &amp; Inclusion</b></h3><p>
Minerva Research Solutions is an <b>Equal Opportunity Employer</b>. We foster a culture where individuals are valued for their unique perspectives, encouraged to challenge the status quo, and empowered to unleash their potential.</p><p>
</p><p>K0ymBxh2d1</p></div>

Call Center Representative (Night Shift)

Explore 936+ Clinical trials quality assurance associate night in Karachi Pakistan this January. Find roles across top companies and apply now to boost your career.

936 clinical trials quality assurance associate night jobs IN Karachi Pakistan

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

US Patient Enrollment Coordinator (Evening Shift)

US Patient Enrollment Coordinator (Evening Shift)

Director, Centre for Regenerative Medicine and Stem Cell Research

Lady Medical Officer

Call Center Representative (Night Shift)