clinical coordinator Jobs in Karachi Pakistan

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clinical psychologist

Karachi vocational training center

<p><b>Karachi Vocational Training Centre (KVTC)</b> is a prestigious institute dedicated to empowering differently abled individuals. At KVTC, we believe in the potential of every individual to learn, grow, and succeed. Through a wide range of therapeutic and educational services, we provide tailored support to help our students achieve confidence and independence.</p><p>We are looking for a committed and compassionate <b>Clinical Psychologist</b> to join our professional team.</p><p><b>Key Responsibilities</b></p><ul><li>Conduct psychological assessments to evaluate students&rsquo; cognitive, emotional, and social development.</li><li>Assist in designing and implementing individualized therapeutic and intervention plans.</li><li>Provide one-on-one and group counseling sessions to support emotional well-being.</li><li>Collaborate with teachers, therapists, and parents to integrate psychological support into daily routines.</li><li>Monitor, document, and track students&rsquo; progress while adjusting interventions when required.</li><li>Support awareness sessions and workshops for parents and staff on mental health and student well-being.</li><li>Maintain confidentiality and ensure ethical psychological practices at all times.</li></ul><p><b>Requirements &amp; Skills</b></p><ul><li>Proven 3 years of experience as a Psychologist or Clinical Psychologist.</li><li>Strong understanding of child psychology, developmental challenges, and therapeutic interventions.</li><li>A patient, empathetic, and professional personality.</li><li>Excellent communication, counseling, and interpersonal skills.</li><li>Minimum qualification: Master&rsquo;s degree in Clinical Psychology.</li></ul><p><b>Location:</b> DHA Phase 4, Karachi</p><p><b>We Offer</b></p><ul><li>Competitive salary</li><li>EOBI</li><li>Health &amp; Life Insurance</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

Clinical Psychologist

Minerva Research Solutions

<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>vapSso9DaM</p></div>

Clinical Trials Quality Assurance Associate (Night)

Hope Global School

<div><h3 class="jobSectionHeader"><b>Job Description</b></h3>
<div>Senior Medical Officer (SMO) leads clinical services, supervises junior doctors, and ensures adherence to medical protocols. They manage patient assessment, diagnosis, and treatment planning in a hospital or clinic setting. The SMO collaborates with multidisciplinary teams to optimise care quality, implements health guidelines, and contributes to policy development. They mentor staff, oversee clinical audits, and support research, ensuring patient safety and continuous improvement in medical services.</div>
<h3 class="jobSectionHeader"><b>Key Responsibilities</b></h3>
<ul><li>Supervise and mentor junior doctors, ensuring clinical excellence and professional growth.</li>
<li>Conduct patient assessments, diagnose illnesses, and develop treatment plans.</li>
<li>Collaborate with multidisciplinary teams for coordinated patient care.</li>
<li>Implement and enforce hospital medical policies and clinical guidelines.</li>
<li>Review and audit clinical cases to maintain high standards of practice.</li>
<li>Participate in continuing medical education and training initiatives.</li>
<li>Lead quality-improvement projects and ensure patient safety systems.</li>
<li>Provide cover for administrative duties and act as clinical lead when required.</li>
</ul><h3 class="jobSectionHeader"><b>Skill &amp; Experience</b></h3>
<ul><li>Excellent diagnostic and clinical decision-making skills under pressure.</li>
<li>Strong leadership and supervisory abilities with good team management.</li>
<li>Effective communication skills with patients and medical colleagues.</li>
<li>Good knowledge of healthcare regulations, guidelines, and hospital protocols.</li>
<li>Ability to conduct clinical audits, research, and quality-improvement projects.</li>
<li>Time management and organisational skills to handle multiple responsibilities.</li>
</ul>
<p><b>Note:</b> Salary is disbursed in the local currency of the country of employment.</p></div>
<br><div></div><div><ul><li><div><div>Date Posted</div>
<div>November 1, 2025</div>
</div></li><div></div><li><div><div>Location</div>
<div><div>Karachi, Pakistan
</div></div></div></li><div></div><li><div><div>Offered Salary:</div>
 <div>3250000 - 4680000 / year</div>
</div></li><div></div><li><div><div>Expiration date</div>
<div>December 17, 2025
</div></div></li><div></div><li><div><div>Experience</div>
<div>1 Year
</div></div></li><div></div><li><div><div>Gender</div>
<div>Both
</div></div></li><div></div><li><div><div>Qualification</div>
<div>Bachelor Degree</div></div></li></ul></div>

Senior Medical Officer

<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>VqJLaFnOod</p></div>

US Patient Enrollment Coordinator (Evening Shift)

Aga Khan Health Services

<div><div><div><div><b>Posted date</b></div> <div>14th November, 2025</div> <div><b>Last date to apply</b></div> <div>23rd November, 2025</div>
</div><br>
<div><div><b>Country</b></div> <div>Pakistan</div> <div><b>Locations</b></div> <div>Karachi</div>
</div><br>
<div><div><b>Category</b></div> <div>Medical Transcription
</div></div><br>
<div><div><b>Type</b></div> <div>Contractual</div> <div><b>Position</b></div> <div>1</div></div></div></div><div></div>
<br><p></p><div><p><b>Aga Khan Health Service, Pakistan (AKHS, P)</b> &mdash; a leading not-for-profit healthcare organization &mdash; is seeking a dynamic and results-oriented professional for the position of <b>Clinical Coordinator</b>.</p>
<p><b>
Position Summary:</b></p>
<p>
The <b>Clinical Coordinator</b> will play a pivotal role in ensuring that all AKHS, P health facilities in Sindh province deliver high-quality, standardized, and patient-centered care. The position focuses on implementing clinical protocols, supporting staff capacity building, achieving regulatory compliance, and fostering a culture of continuous improvement and accountability.</p>
<p>
The incumbent will work closely with nursing and medical staff, quality assurance teams, and management to align daily clinical practices with AKHS&rsquo;s quality and safety standards while supporting the organization&rsquo;s commitment to sustainability and operational excellence.</p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li><b>Elevate Quality:</b> Transform community health centers into models of safe, patient-centered, and reliable care.</li>
<li><b>Standardize Practices:</b> Keep clinical and nursing protocols updated, practical, and aligned with national and international best practices.</li>
<li><b>Capacity Building:</b> Lead and facilitate technical training, mentorship, and coaching programs to strengthen clinical skills, decision-making, and teamwork.</li>
<li><b>Certification &amp; Compliance:</b></li>
<li>Ensure all facilities maintain compliance with AKHS standards and local regulatory/licensing requirements.</li>
<li>Lead and coordinate certification or accreditation efforts across sites.</li>
<li><b>Patient Feedback &amp; Experience:</b> Design and oversee systems to capture, analyze, and act on patient feedback, ensuring prompt resolution of complaints and continuous service improvement.</li>
<li><b>Monitoring &amp; Audits:</b> Lead clinical audits, root-cause analyses, and continuous improvement initiatives, working closely with nurses, consulting doctors, and leadership teams.</li>
</ul>
<p><b>Key Milestones in the First Six Months</b></p>
<ul>
<li>Clinical guidelines are updated and implemented across all sites within six months.</li>
<li>Nursing and doctor teams feel confident, supported, and empowered to deliver excellent care.</li>
<li>Patient feedback systems are functional and responsive.</li>
<li>Clinics are on track for or have achieved certification milestones.</li>
<li>Facilities maintain full compliance with all licensing and regulatory requirements.</li>
<li>A data-driven culture of continuous quality improvement is embedded across the region.</li>
<li>Clear steps are underway toward reducing environmental impact.</li>
</ul>
<p><b>Qualification &amp; Experience</b></p>
<ul>
<li>BScN or MScN.</li>
<li>Minimum 2 years of relevant experience in clinical coordination, quality improvement, or healthcare operations.</li>
<li>Passionate about clinical excellence, patient safety, and quality standards.</li>
<li>Ability to translate clinical guidelines into action through coaching and supervision of nurses and consulting doctors.</li>
<li>Solid understanding of regulatory frameworks and licensing requirements within Sindh.</li>
<li>Strong leadership, communication, and team collaboration skills across multidisciplinary teams.</li>
<li>Analytical, proactive, and committed to continuous learning and improvement.</li>
<li>Demonstrates integrity, empathy, and precision in decision-making and operations.</li>
</ul>
<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 are expected to take part in making this a reality. The Clinical Coordinator, accompanied with his/her Line Manager(s) 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><b>
Note: Only shortlisted candidates will be contacted for an interview.</b></p></div><p></p>

Clinical Coordinator

Teksoft Solutions

<p><b>Job Title:</b> Back-End Support Executive (Clinical Operations) &mdash; Night Shift</p><p><b>Location:</b> Gulshan-e-Iqbal, Block 4, Karachi (Onsite)</p><p><b>Qualification:</b> <b>MBBS required</b></p><p>About the Role</p><p>We support US-based physicians caring for patients in <b>hospitals, Skilled Nursing Facilities (SNF), Assisted Living Facilities (ALF), and home-based/telehealth</b> programs. As a Back-End Support Executive, you will work the <b>night shift</b> to review patient information across multiple EHRs, prepare concise clinical notes, and <b>escalate priority issues</b> to the on-call US doctor in real time (primarily via <b>Google Chat</b> voice/text).</p><p>Key Responsibilities</p><ul><li><b>Chart Review &amp; Data Abstraction</b></li><li><b>Review admission notes, progress notes, vitals, I/O, labs, imaging, and orders across different EHRs.</b></li><li>Track trends in <b>vitals, labs, and test results</b> (e.g., BP/HR/SpO&#8322;, CBC/CMP, troponin, INR, A1c, renal panel).</li><li><b>Clinical Documentation</b></li><li><b>Draft clear clinical notes</b> in the EHR aligned to patient condition and physician directives.</li><li><b>Add encounter information</b> and update problem lists/medication lists/allergies after physician visits.</li><li>Maintain accurate <b>time-stamped logs</b> of all actions taken and communications sent/received.</li><li><b>Triage &amp; Escalation</b></li><li><b>Prioritize and escalate</b> 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><b>Communication</b></li><li><b>Work directly with US physicians via Google Chat (voice notes + text)</b>; capture and implement instructions precisely.</li><li>Coordinate with internal teams to resolve EHR access issues, missing data, or documentation gaps.</li><li><b>Compliance &amp; Quality</b></li><li><b>Adhere to HIPAA/PHI confidentiality, organizational SOPs, and documentation standards.</b></li><li>Meet SLAs and quality targets for <b>accuracy, completeness, and turnaround time</b>.</li></ul><p>Required Qualifications &amp; Skills</p><ul><li><b>MBBS</b> (mandatory).</li><li>Comfortable working <b>night shifts</b> aligned to US hours.</li><li>Strong grasp of <b>medical terminology</b>, clinical reasoning, and basic interpretation of vitals/labs.</li><li>Excellent <b>written and verbal communication</b> in English; crisp, structured clinical summaries.</li><li>High <b>attention to detail</b>, reliability, and sound <b>decision-making</b> under time constraints.</li><li>Hands-on with <b>EHR systems</b> (any), Google Workspace (Docs/Sheets), and <b>Google Chat</b>.</li><li>Fast, accurate typing; disciplined task tracking and follow-through.</li></ul><p><b>Nice to Have</b></p><ul><li>Prior experience in <b>clinical operations, hospitalist programs, RPM/CCM</b>, 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><p>Shift, Employment Type &amp; Location</p><ul><li><b>Shift:</b> Night (US hours) &mdash; exact schedule shared during interviews.</li><li><b>Type:</b> Full-time, onsite.</li><li><b>Office:</b> <b>Gulshan-e-Iqbal, Block 4, Karachi.</b></li></ul><p>Performance KPIs (what success looks like)</p><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><p>What We Offer</p><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><p>How to Apply</p><p>Send your <b>CV</b> and a short note on relevant experience to <b>career@teksoft.net</b> with subject:</p><ul><li><b>Back-End Support Executive (Night Shift) &mdash; MBBS</b>.</li></ul><p>Job Type: Full-time</p><p>Application Question(s):</p><ul><li>Expected Salary?</li><li>Comfortable with night shifts? 5PM to 2AM or 6PM to 3AM?</li><li>Any notice period?</li></ul><p>Work Location: In person</p><p>Expected Start Date: 15/11/2025</p>

Back-End Support Executive (Clinical Operations) — Night Shift

HRCONSOL

<p><b>Key ResponsibilitiesClinical Oversight &amp; Quality Assurance</b></p><ul><li>Conduct regular audits of medical officers&rsquo; performance, SOAP notes, and case documentation.</li><li>Conduct at least two physical audits per doctor annually.</li><li>Monitor compliance with clinical protocols, guidelines, and ethical standards.</li><li>Review and analyze EMR data for accuracy, completeness, and effective utilization.</li><li>Identify performance gaps and recommend corrective actions for improvement.</li></ul><p><b>Training &amp; Capacity Building</b></p><ul><li>Develop, organize, and conduct Continuing Medical Education (CME) sessions and refresher trainings for medical staff.</li><li>Evaluate training needs based on audit findings and clinical performance trends.</li><li>Ensure all CME content aligns with current medical standards and organizational goals.</li><li>Develop and implement comprehensive orientation programs for doctors, ensuring smooth onboarding and familiarization with policies, protocols, EMR systems, and workflows.</li></ul><p><b>Operational Management</b></p><ul><li>Oversee and manage doctors&rsquo; schedules, rotations, and leave plans to ensure uninterrupted service delivery.</li><li>Coordinate with HR and Operations teams for staffing and coverage requirements.</li><li>Support the development of clinical presentations, reports, and dashboards for internal and external stakeholders.</li></ul><p><b>Policy &amp; Protocol Development</b></p><ul><li>Review and update clinical SOPs, protocols, and policies to ensure compliance and relevance.</li><li>Collaborate with the management team to implement evidence-based practices.</li><li>Ensure all documentation and operational activities comply with organizational and regulatory standards.</li></ul><p><b>Monitoring, Reporting &amp; Coordination</b></p><ul><li>Prepare regular performance and compliance reports for management review.</li><li>Coordinate with technical and operational teams to streamline documentation and reporting.</li><li>Provide administrative support in audits, program evaluations, and donor compliance reviews.</li></ul><p><b>Requirements</b></p><ul><li>MBBS / MCPS (or equivalent).</li><li>4&ndash;6 years of experience in healthcare administration, clinical management, or supervision.</li><li>Strong understanding of clinical workflows, EMR systems, and quality assurance mechanisms.</li><li>Excellent leadership, analytical, and communication skills.</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

Medical Administrator

Explore 52+ Clinical psychologist in Karachi Pakistan this November. Find roles across top companies and apply now to boost your career.