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internship medical billing (night shift)

(night-shift) junior human resource executive Jobs in Karachi

accounting quality controller (audit & financial reporting) Jobs in Karachi

assistant manager: surveillance (night shift) Jobs in Karachi

clinical trials quality assurance associate night

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)
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Clinical Trials Quality Assurance Associate (Night)

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

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

Legendesk

Responsibilities:<ul><li>Ensure all products meet or exceed quality standards and customer expectations.</li><li>Identify and document any defects or issues and ensure they are addressed promptly.</li><li>Perform root cause analysis on identified defects and implement corrective actions.</li><li>Work with cross-functional teams (specially with the international sales team) to develop and implement quality improvement.</li></ul>Requirements:<ul><li>Fresh to 6 months of experience in a quality assurance role.</li><li>Excellent analytical and problem-solving skills.</li><li>Good communication and interpersonal skills.</li><li>Good in report and email writing.</li></ul>Location: Karachi, DHA Phase 6 (on-site)Shift: Night (7 pm to 4 am)Benefits:<ul><li>Pick &amp; drop.</li><li>Foodpanda.</li><li>Provident fund.</li><li>Paid leaves.</li><li>Medical.</li></ul>Job Type: Full-timePay: Rs40,000.00 - Rs50,000.00 per monthApplication Question(s):<ul><li>Available for night shift with pick and drop?</li></ul>Location:<ul><li>Karachi Defence Housing Society (Required)</li></ul>Work Location: In person

QA Executive - Billing

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

Teksoft Solutions

Job Title: Back-End Support Doctors (Clinical Operations) &mdash; Night ShiftLocation: Gulshan-e-Iqbal, Block 4, Karachi (Onsite)Qualification: MBBS requiredAbout the RoleWe support US-based physicians caring for patients in hospitals, Skilled Nursing Facilities (SNF), Assisted Living Facilities (ALF), and home-based/telehealth programs. As a Back-End Support Executive, you will work the night shift to review patient information across multiple EHRs, prepare concise clinical notes, and escalate priority issues to the on-call US doctor in real time (primarily via Google Chat voice/text).Key Responsibilities:<ul><li>Chart Review &amp; Data Abstraction</li><li>Review admission notes, progress notes, vitals, I/O, labs, imaging, and orders across different EHRs.</li><li>Track trends in vitals, labs, and test results (e.g., BP/HR/SpO₂, CBC/CMP, troponin, INR, A1c, renal panel).</li><li>Clinical Documentation</li><li>Draft clear clinical notes in the EHR aligned to patient condition and physician directives.</li><li>Add encounter information and update problem lists/medication lists/allergies after physician visits.</li><li>Maintain accurate time-stamped logs of all actions taken and communications sent/received.</li><li>Triage &amp; Escalation</li><li>Prioritize and escalate abnormal findings to the US physician according to the escalation matrix (e.g., critical labs, significant vitals deviation, rapid clinical changes).</li><li>Summarize cases succinctly (chief issue &rarr; pertinent findings &rarr; objective data &rarr; current status &rarr; requested action).</li><li>Communication</li><li>Work directly with US physicians via Google Chat (voice notes + text); capture and implement instructions precisely.</li><li>Coordinate with internal teams to resolve EHR access issues, missing data, or documentation gaps.</li><li>Compliance &amp; Quality</li><li>Adhere to HIPAA/PHI confidentiality, organizational SOPs, and documentation standards.</li><li>Meet SLAs and quality targets for accuracy, completeness, and turnaround time.</li></ul>Required Qualifications &amp; Skills<ul><li>MBBS (mandatory).</li><li>Comfortable working night shifts aligned to US hours.</li><li>Strong grasp of medical terminology, clinical reasoning, and basic interpretation of vitals/labs.</li><li>Excellent written and verbal communication in English; crisp, structured clinical summaries.</li><li>High attention to detail, reliability, and sound decision-making under time constraints.</li><li>Hands-on with EHR systems (any), Google Workspace (Docs/Sheets), and Google Chat.</li><li>Fast, accurate typing; disciplined task tracking and follow-through.</li></ul>Nice to Have<ul><li>Prior experience in clinical operations, hospitalist programs, RPM/CCM, or back-office physician support.</li><li>Familiarity with US payer/clinical workflows and common EHRs (e.g., Epic, PCC, Athena, eCW, Elation, etc.).</li></ul>Shift, Employment Type &amp; Location<ul><li>Shift: Night (US hours) &mdash; exact schedule shared during interviews.</li><li>Type: Full-time, onsite.</li><li>Office: Gulshan-e-Iqbal, Block 4, Karachi.</li></ul>Performance KPIs (what success looks like)<ul><li>Documentation accuracy &amp; completeness.</li><li>Turnaround time from data review to escalation.</li><li>Adherence to escalation matrix and SOPs.</li><li>Communication clarity and responsiveness.</li><li>Compliance (HIPAA/PHI) and zero data-handling incidents.</li></ul>What We Offer<ul><li>Structured onboarding with SOPs, escalation matrix, and EHR workflows.</li><li>Continuous coaching and clear growth paths in clinical operations.</li><li>Market Competitive Salary</li><li>Health Insurance</li><li>Door to Door Pick and Drop for female candidates.</li></ul>How to ApplySend your CV and a short note on relevant experience to career@teksoft.net with subject:<ul><li>Back-End Support Executive (Night Shift) &mdash; MBBS.</li></ul>Or apply directly on IndeedPay: Rs80,000.00 - Rs120,000.00 per monthApplication Question(s):<ul><li>Expected Salary?</li><li>Any notice period?</li><li>Comfortable with night shifts? 5PM to 2AM or 6PM to 3AM?</li></ul>Work Location: In person

Back End Support Doctors

Human Capital HR Solutions

Associate Project Manager &ndash; Agile &amp; QALocation: Karachi, Pakistan Industry: IT Sector (Canadian-Based Client) Employment Type: Full-TimeHuman Capital is hiring on behalf of its Canadian-based client in the IT industry. We are seeking a detail-oriented and proactive Associate Project Manager who can effectively coordinate with engineering teams while also supporting quality assurance and release processes.Role OverviewThis role combines project coordination, Agile execution, and hands-on quality assurance. The ideal candidate will play a key role in ensuring timely delivery and maintaining high product quality across web and mobile applications.Key Responsibilities<ul><li>Plan, track, and manage project timelines, tasks, and deliverables</li><li>Assist in sprint planning, daily stand-ups, reviews, and retrospectives (Agile)</li><li>Coordinate effectively between developers, QA teams, and stakeholders</li><li>Identify project risks and blockers, ensuring timely resolution</li><li>Perform manual testing of web and mobile applications</li><li>Design, create, and execute test cases and test scenarios</li><li>Log, track, and document bugs with clarity and detail</li><li>Validate bug fixes and support release readiness</li><li>Maintain proper documentation and ensure alignment across tasks and teams</li></ul>Requirements<ul><li>1&ndash;2 years of experience in Project Management, QA, or coordination roles</li><li>Strong understanding of Agile methodologies (Scrum/Kanban)</li><li>Hands-on experience with manual testing</li><li>Experience testing web and mobile applications</li><li>Strong communication, coordination, and organizational skills</li><li>Ability to manage multiple tasks and meet deadlines</li><li>Experience working closely with engineering teams</li></ul>How to Apply:<ul><li>Send your CV to: careers1.hc@gmail.com</li><li>CC: careers@humancapitalintl.com</li><li>Subject Line: &ldquo;Associate Project Manager &ndash; Agile &amp; QA&rdquo;</li><li>Follow our social accounts for the latest job opportunities:</li><li>	Instagram: https://www.instagram.com/humancapitalhrsolutions/</li><li>	LinkedIn: https://www.linkedin.com/company/human-capital-hr-solution/</li><li>	Facebook: https://www.facebook.com/humancapitalhrsolution/</li></ul>Job Type: Full-timeWork Location: In person

Associate Project Manager – Agile & QA

Explore 1185+ Clinical trials quality assurance associate night in Karachi this May. Find roles across top companies and apply now to boost your career.