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technician clinical trials unit

Aga Khan University

<div><div>Technician, Clinical Trials Unit - (260001MZ)</div><div><div> 
</div>Technician, Clinical Trials Unit
Location: Karachi, Pakistan
Introduction
Aga Khan University, chartered in 1983 as Pakistan's first private international university, is committed to the provision of education, research, and health care of international standards relevant to Pakistan and the region. The affiliated Aga Khan University Hospital provides state-of-the-art clinical facilities and well-equipped diagnostic services. The University currently has teaching sites in Pakistan, East Africa, the United Kingdom, and Afghanistan, and is a major component of Aga Khan Development Network.
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.
Clinical Trials Unit (CTU) is a Department dedicated to develop a center of excellence for high quality and high impact clinical trials both nationally &amp; internationally. The Department promotes AKU&rsquo;s vision by providing leadership, consultation, and facilitation in different phases of clinical trials in compliance with the International Standards and Good Clinical Practice (GCP) guidelines.
This is a grant-funded contractual position.
Responsibilities
You will be responsible to:<ul><li>
ensure compliance with departmental policies and procedures and JCIA standards</li><li>
maintain assigned work areas and equipment in a clean and orderly condition</li><li>
accurately fill drug/medication cassettes</li><li>
ensure timely delivery of medications to the right location and various points of dispensing, including scanning of documents and assisting pharmacists during QC audits</li><li>
handle large and heavy drug cartons and place them on shelves</li><li>
ensure inventory management, including receipt of shipments, placement of stock, lot and expiry control, and FIFO (first-in, first-out) arrangement</li><li>
generate PR/MSR (purchase requisition/material stock requisition) for consumables and maintain adequate supplies</li><li>
assist pharmacists during audits and related activities in maintaining pharmacy records</li><li>
assist pharmacists in training new employees.</li></ul></div><div></div><div><div> 
</div>Requirements
You should have:<ul><li>
intermediate; graduate qualification will be preferred; a dispenser diploma will be an added advantage</li><li>
at least one year of experience working in a hospital pharmacy, community pharmacy, or clinical setting</li><li>
good knowledge of basic pharmacy operations</li><li>
knowledge of key medications, medical supplies, and dosage forms</li><li>
ability to read labels, drug names, and differentiate between similar medicines</li><li>
ability to work on computers with skills in MS Office and institutional software (SAHL and PeopleSoft)</li><li>
fluency in Urdu and the ability to read and write basic English.</li></ul>
Comprehensive employment reference checks will be conducted.<div> 
</div></div><div>
Primary Location: Pakistan-Karachi</div><div>
Organisation: Aga Khan University Pakistan</div><div>
Employee Status: Contractual</div><div>
Job Type: Standard</div><div>
Job Posting: 17/04/2026, 4:23:57 AM</div><div>
Closing Date: 30/04/2026, 1:59:00 PM</div></div>

Technician, Clinical Trials Unit

DM Clinical Research

<div>The IT Manager &ndash; Clinical Trials is responsible for overseeing the design, implementation, security, and ongoing support of IT systems that enable clinical trial operations. This role manages cloud-based infrastructure across Microsoft Azure and Google Cloud Platform (GCP), supports validated clinical systems, ensures regulatory compliance (GxP, HIPAA, 21 CFR Part 11), and partners closely with Clinical Operations, Data Management, and Engineering teams. The role combines people leadership, cloud architecture oversight, vendor management, and compliance ownership in a regulated clinical research environment.
DUTIES &amp; RESPONSIBILITIES
IT Operations &amp; Service Management<ul><li>
Lead IT operations including incident management, change management, and problem resolution</li><li>
Define and maintain IT policies, SOPs, and runbooks</li><li>
Manage SLAs with internal teams and external vendors</li></ul>
Cloud &amp; Infrastructure Management<ul><li>
Own and manage cloud infrastructure across Azure and GCP, including compute, networking, storage, databases, and security services</li><li>
Ensure high availability, scalability, disaster recovery, and cost optimization of cloud environments</li><li>
Oversee hybrid and multi-cloud architectures supporting clinical trial platforms</li><li>
Manage identity and access using Azure AD / IAM, role-based access control (RBAC), and least-privilege principles</li><li>
Support end-user IT needs related to clinical systems and secure access</li></ul>
Clinical Systems &amp; Applications<ul><li>
Support IT systems used in clinical trials (e.g., CTMS, eTMF, EDC, patient engagement platforms, AI/telephony systems)</li><li>
Partner with engineering teams supporting custom platforms (e.g., patient management, communications, integrations)</li><li>
Ensure validated system lifecycle management (CSV/CSA) for GxP systems</li><li>
Oversee system integrations, APIs, and data flows between internal platforms and third-party SaaS Vendors</li></ul>
Security, Compliance &amp; Risk<ul><li>
Ensure compliance with HIPAA, GDPR, GxP, 21 CFR Part 11, SOC 2, and internal security policies</li><li>
Lead audit readiness, vendor assessments, and security reviews</li><li>
Implement monitoring, logging, incident response, and vulnerability management</li><li>
Own data protection strategies including encryption, backup, retention, and access auditing</li></ul>
Leadership &amp; Collaboration<ul><li>
Manage and mentor IT staff and/or contractors</li><li>
Act as a trusted IT partner to Clinical Operations, QA, Compliance, Product, and Engineering teams</li><li>
Translate clinical and business requirements into secure, scalable technical solutions</li><li>
Participate in technology roadmap planning and platform modernization initiatives</li></ul>
KNOWLEDGE &amp; EXPERIENCE
Education &amp; Experience<ul><li>
Bachelor&rsquo;s degree in Information Technology, Computer Science, or related field (or equivalent experience)</li><li>
7+ years of progressive IT experience, including 3+ years in a leadership or managerial role</li><li>
Direct experience supporting clinical trials, life sciences, healthcare, or regulated environments</li></ul>
Credentials:<ul><li>
Associate Google Workspace Administrator (preferred)</li></ul>
Knowledge and Skills:<ul><li>
Strong hands-on and architectural experience with Microsoft Azure</li><li>
Working knowledge of Google Cloud Platform (GCP)</li><li>
Experience with cloud databases (SQL, NoSQL), networking, and API-based systems</li><li>
Familiarity with DevOps, CI/CD, and infrastructure-as-code concepts</li><li>
Understanding of system validation and computerized system assurance (CSV/CSA)</li></ul></div>

IT Manager

Minerva Research Solutions

<div>JOB DESCRIPTION: 
 
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.
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. 
 
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. 
 
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.
Responsibilities:<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>
Knowledge, Education, and Experience:<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>
Skills and Abilities:<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>
Benefits:<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>
Openings:
04 positions 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
Evening Shift (06 PM to 02 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
AjYqzsoJFy</div>

Clinical Trials Quality Assurance Associate (Night)

Mac Care

Job SummaryWe are seeking a detail-oriented Clinical Data Analyst with strong expertise in healthcare analytics and hands-on experience working with clinical research data. This role will support our Value-Based Care (VBC) and MSSP initiatives, while also contributing to the analysis and interpretation of clinical datasets from research and quality improvement programs.The ideal candidate will transform complex healthcare and clinical research data into actionable insights to improve patient outcomes, ensure regulatory compliance, and drive data-informed decision-making.Key Responsibilities<ul><li>Analyze and manage CCLF, HCC, and quality data for MSSP and Value-Based Care programs.</li><li>Work with clinical research datasets (e.g., study data, patient cohorts, outcomes data) to support research analysis and reporting.</li><li>Develop and maintain interactive dashboards using Power BI to track performance, clinical outcomes, and quality metrics.</li><li>Perform data extraction, transformation, and cleaning using Power Query and SQL.</li><li>Collaborate with clinical, research, and operations teams to identify high-risk populations and monitor quality measures.</li><li>Support CMS reporting, risk adjustment analysis, and quality improvement initiatives.</li><li>Assist in clinical study data validation, reconciliation, and audit readiness.</li><li>Ensure data integrity, accuracy, and compliance with healthcare regulations (HIPAA, CMS guidelines).</li><li>Translate complex datasets into clear insights and recommendations for leadership and stakeholders.</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Computer Science, Data Analytics, Public Health, Biostatistics, or a related field.</li><li>2&ndash;4 years of experience in healthcare data analytics, clinical research data analysis, or value-based care programs.</li><li>Hands-on experience working with clinical datasets, research data, or population health data.</li></ul>Technical Skills<ul><li>Power BI (2+ years) &ndash; dashboarding and visualization</li><li>Power Query (2&ndash;3 years) &ndash; data transformation</li><li>SQL &ndash; data extraction and manipulation</li><li>Strong skills in data cleaning, validation, and analysis</li></ul>Domain Knowledge<ul><li>Understanding of CMS programs, MSSP, and HCC risk adjustment</li><li>Familiarity with clinical research processes, datasets, and reporting standards</li><li>Experience with EMR/EHR systems and population health tools</li></ul>Preferred Qualifications<ul><li>Experience supporting clinical trials, registry data, or outcomes-based research</li><li>Knowledge of study design, cohort analysis, and healthcare quality measures (e.g., HEDIS)</li><li>Exposure to statistical tools (R, Python, or similar) is a plus</li></ul>Job Type: Full-timeWork Location: In person

Clinical Data Analyst

Job SummaryWe are seeking a detail-oriented Clinical Data Analyst with strong expertise in healthcare analytics, hands-on experience working with clinical research data, and practical experience using Athena EMR/EHR systems. This role will support our Value-Based Care (VBC) and MSSP initiatives, while also contributing to the analysis and interpretation of clinical datasets from research and quality improvement programs.The ideal candidate will transform complex healthcare and clinical research data into actionable insights to improve patient outcomes, ensure regulatory compliance, and drive data-informed decision-making.Key Responsibilities<ul><li>Analyze and manage CCLF, HCC, and quality data for MSSP and Value-Based Care programs.</li><li>Work with clinical research datasets (e.g., study data, patient cohorts, outcomes data) to support research analysis and reporting.</li><li>Extract, validate, and analyze patient and operational data from Athena EMR and other healthcare systems.</li><li>Develop and maintain interactive dashboards using Power BI to track performance, clinical outcomes, and quality metrics.</li><li>Perform data extraction, transformation, and cleaning using Power Query and SQL.</li><li>Collaborate with clinical, research, and operations teams to identify high-risk populations and monitor quality measures.</li><li>Support CMS reporting, risk adjustment analysis, and quality improvement initiatives.</li><li>Assist in clinical study data validation, reconciliation, and audit readiness.</li><li>Ensure data integrity, accuracy, and compliance with healthcare regulations (HIPAA, CMS guidelines).</li><li>Translate complex datasets into clear insights and recommendations for leadership and stakeholders.</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Computer Science, Data Analytics, Public Health, Biostatistics, or a related field.</li><li>2&ndash;4 years of experience in healthcare data analytics, clinical research data analysis, or value-based care programs.</li><li>Hands-on experience working with clinical datasets, research data, or population health data.</li><li>Experience working with Athena EMR/EHR systems for reporting, patient data extraction, workflow analysis, or operational support.</li></ul>Technical Skills<ul><li>Power BI (2+ years) &ndash; dashboarding and visualization</li><li>Power Query (2&ndash;3 years) &ndash; data transformation</li><li>SQL &ndash; data extraction and manipulation</li><li>Experience navigating and reporting from Athena EMR</li><li>Strong skills in data cleaning, validation, and analysis</li></ul>Domain Knowledge<ul><li>Understanding of CMS programs, MSSP, and HCC risk adjustment</li><li>Familiarity with clinical research processes, datasets, and reporting standards</li><li>Experience with EMR/EHR systems, especially Athenahealth / Athena EMR, and population health tools</li></ul>Preferred Qualifications<ul><li>Experience supporting clinical trials, registry data, or outcomes-based research</li><li>Knowledge of study design, cohort analysis, and healthcare quality measures (e.g., HEDIS)</li><li>Exposure to statistical tools such as R or Python is a plus</li></ul>Job Type: Full-timeWork Location: In person

Clinical Data Analyst (Athena Experience Required)

<div><div>Assistant Head Nurse, Well Baby Nursery, Department of Paediatrics - (260001FU)</div><div><div> 
</div>Assistant Head Nurse, Well Baby Nursery, Department of Paediatrics

Entity: Aga Khan University

Location: Karachi

Introduction to the Aga Khan University:

Chartered in 1983, Aga Khan University (AKU) is a private, autonomous, and self-governing international university with 13 teaching sites in 6 countries distributed across three continents. As an integral part of the Aga Khan Development Network, AKU provides higher education in several disciplines, carries out research pertinent to the countries in which it exists and has campuses, programs and/or teaching hospitals in Afghanistan, Kenya, Pakistan, Tanzania, Uganda, and the UK. As an international institution, AKU operates on the core principles of quality, relevance, impact, and access; and AKU is a model of academic excellence and an agent of social change.

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.

Job Roles/Responsibilities:

You will be responsible to:
<ul>
<li>effective patient care management by assessing patients critically, participating in patient care rounds with physician to monitor the quality of the patient care/ environment, responding quickly and appropriately in conflict or crisis in patient care areas and ensure all reportable cases are communicated to HN nurse manager verbally and through shift reports</li>
<li>plan nursing care and health teaching for patients according to theirs need, ensure completion of nursing assessment for all patients by assigned staff in line with standards procedures, and order to report patients&rsquo; condition accurately to the physicians / supervisor</li>
<li>participate actively in quality improvement projects / nursing research projects / special projects at unit level.</li>
<li>periodically review nursing documentation of patient care of delegated area</li>
<li>allocate assignment on a regular basis and in emergency situation and/or during weekend and public holiday , to team members based on their skill and experience for adequate staff care for patient care management</li>
<li>assess nursing staff learning needs, offer suggestion and materials for students&rsquo; experience, in order to enhance their clinical learning experience on the wards</li>
<li>provide mentorship for staff/ students and reinforce the unit philosophy and goals to all staffs</li></ul></div><div></div><div><div> 
</div>Requirements:

You must have:
<ul>
<li>Baccalaureate in Nursing degree from a recognized school of nursing, preferably a Masters degree in the same</li>
<li>Current registration from Pakistan Nursing Council</li>
<li>Certification in Basic Life Support, ACLS, PALS, NRP provider, , Safe Medication Administration, Intravenous Cannulation and procedural sedatio</li>
<li>At least two years&rsquo; experience as a nurse</li>
<li>Ability to assess, plan and manage patient care with expertise as per protocols</li>
<li>Familiarity with the involvement in the concept of QINP</li>
<li>Sound clinical knowledge and management competencies.</li>
<li>Excellent interpersonal skills and ability to meet stringent deadlines</li>
<li>Ability to effectively work in shifts as well as independently.</li>
</ul>
Comprehensive employment reference checks will be conducted.<div> 
</div></div><div>
Primary Location: Pakistan-Karachi</div><div>
Organisation: Aga Khan Hospital &amp; Medical College</div><div>
Employee Status: Regular</div><div>
Job Type: Standard</div><div>
Job Posting: 09/04/2026, 7:37:18 AM</div><div>
Closing Date: 19/04/2026, 1:59:00 PM</div></div>

Assistant Head Nurse, Well Baby Nursery, Department of Paediatrics

Arc Inventor

Key Responsibilities<ul><li>Product-Led Content Creation: Write in-depth blog posts, &quot;how-to&quot; guides, and white papers that demonstrate how our SaaS solution solves specific pain points for our target Ideal Customer Profile (ICP).</li><li>Documentation &amp; Knowledge Base: Develop and maintain user-facing documentation, API references, and FAQs to help users self-serve and reduce support ticket volume.</li><li>Cross-Functional Collaboration: Partner with Product Managers and Engineers to understand new features, and with Marketing to align content with SEO and lead-generation goals.</li><li>Simplify Complexity: Translate technical jargon and &quot;engineering-speak&quot; into clear, benefit-driven narratives for both technical (developers) and non-technical (executives) audiences.</li><li>Multi-Channel Strategy: Repurpose long-form technical content into social media snippets (LinkedIn), email newsletters, and video scripts to maximize reach.</li><li>SEO Optimization: Conduct keyword research and implement SEO best practices to ensure our technical content ranks for high-intent search queries.</li></ul>Required Skills &amp; Qualifications<ul><li>Experience: 3+ years of experience in technical writing or content marketing, specifically within a B2B SaaS environment.</li><li>Tool Proficiency: Experience with documentation and CMS tools (e.g., Zendesk, GitBook, WordPress, Confluence) and SEO tools (e.g., Ahrefs, Semrush).</li><li>Strategic Thinking: Understanding of the SaaS marketing funnel (ToFu, MoFu, BoFu) and how content drives trials and renewals.</li><li>Attention to Detail: Impeccable grammar and the ability to maintain a consistent brand voice across all technical materials.</li></ul>Job Type: Full-timeWork Location: In personWork Location: In person

Technical Content Writer (SAAS Based)

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