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implementation consultant

associate clinical consultant

CureMD

<div>
 <strong>
  Job Overview:
  <br/>
  <br/>
 </strong>
 Transform patient care through AI and technology as an
 <strong>
  Associate
 </strong>
 <strong>
  Clinical Consultant
 </strong>
 at our cutting-edge EMR and AI healthcare solutions company, where innovation meets clinical expertise. Dive into a dynamic role that blends evidence-based content development, workflow optimization, and collaborative problem-solving&mdash;with the added opportunity to help shape the future of AI-driven healthcare delivery.
 <br/>
 <br/>
 <strong>
  Job Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Develop and maintain clinical content, including treatment pathways, order sets, and documentation templates for various medical specialties.
  </li>
  <li>
   Analyze clinical workflows to identify areas for improvement and implement data-driven, AI-enhanced solutions to boost efficiency and patient care.
  </li>
  <li>
   Collaborate with clinicians, healthcare providers, and other stakeholders to ensure clinical content is evidence-based, up-to-date, and aligned with the latest medical guidelines.
  </li>
  <li>
   Work closely with the EMR and AI development teams to seamlessly integrate clinical content and intelligent workflows into the software ecosystem.
  </li>
  <li>
   Participate in user acceptance testing to ensure clinical content and workflows function as intended within the EMR and AI modules.
  </li>
  <li>
   Provide training and support to clinicians and other end-users on effectively utilizing the clinical content and intelligent workflows within the EMR.
  </li>
  <li>
   Collaborate with top-tier healthcare professionals and our agile tech team to continuously enhance clinical modules.
  </li>
  <li>
   Drive measurable improvements in patient care, decision support, and clinical efficiency through innovative digital health and AI initiatives.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   MBBS degree from a HEC Recognized University.
  </li>
  <li>
   Familiarity with EMR systems, clinical workflows, and healthcare informatics.
  </li>
  <li>
   Knowledge of medical terminologies and coding systems (e.g., ICD-10, CPT, SNOMED CT).
  </li>
  <li>
   Experience in clinical research, data analysis, and content development.
  </li>
  <li>
   Strong understanding of evidence-based medicine and clinical practice guidelines.
  </li>
  <li>
   Excellent analytical and problem-solving skills.
  </li>
  <li>
   Strong communication and interpersonal skills to effectively collaborate with cross-functional teams.
  </li>
  <li>
   Detail-oriented with a commitment to accuracy and quality.
  </li>
  <li>
   Ability to manage multiple projects simultaneously and meet tight deadlines.
  </li>
  <li>
   Minimum of 2-3 years of experience in a similar role, preferably in an EMR or healthcare technology setting.
  </li>
  <li>
   Familiarity with US Healthcare system is preferred.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compensation and Benefits:
  <br/>
  <br/>
 </strong>
 <strong>
  💰 Financial:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive salary and bi-annual bonus.
  </li>
  <li>
   Fast track and uncapped career growth for high performers.
  </li>
  <li>
   Company-sponsored vehicle financing (car and bike).
  </li>
  <li>
   Interest-free loans.
  </li>
  <li>
   Provident Fund: CureMD matches up to 8% of your base salary.
  </li>
  <li>
   Fuel Card.
  </li>
  <li>
   Cellular Allowance.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  🏥 Health and Wellness:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   In-house clinic with a team of certified male and female doctors with 24/7 telemedicine service.
  </li>
  <li>
   Hospital treatment monitoring by company doctors.
  </li>
  <li>
   Comprehensive health coverage for your immediate family (outpatient, inpatient, maternity and parents' inpatient).
  </li>
  <li>
   Exclusive health benefits and discounts at top class clinics and labs.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  🤝🏻 Supportive Workplace:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Pick-up and drop-off services for female employees.
  </li>
  <li>
   In-house daycare facility.
  </li>
  <li>
   In-house gym and recreational area to unwind.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  📚 Continued Learning:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Company-sponsored trainings, workshops, development programs and retreats.
  </li>
  <li>
   Paid specialized trainings/certifications.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  The Difference You&rsquo;ll Make:
  <br/>
  <br/>
 </strong>
 At CureMD, every role, whether senior or junior, plays a pivotal part in transforming healthcare. By joining our innovative team, you&rsquo;ll contribute to groundbreaking technology that directly impacts patient care, enhances healthcare efficiency, and saves lives globally. Your skills and passion will drive meaningful change, helping us deliver solutions that support healthcare professionals in critical, real-time settings. Together, we&rsquo;re not just advancing technology &mdash; we&rsquo;re making a tangible difference in people&rsquo;s lives.
 <strong>
  Together, let&rsquo;s save lives
 </strong>
 .
</div>


Associate Clinical Consultant

<div><div>Job Overview:</div><div></div><div>
Transform patient care through AI and technology as an Associate Clinical Consultant at our cutting-edge EMR and AI healthcare solutions company, where innovation meets clinical expertise. Dive into a dynamic role that blends evidence-based content development, workflow optimization, and collaborative problem-solving&mdash;with the added opportunity to help shape the future of AI-driven healthcare delivery.</div><div><br>
Job Responsibilities:</div><div></div><ul><li>Develop and maintain clinical content, including treatment pathways, order sets, and documentation templates for various medical specialties.</li><li>Analyze clinical workflows to identify areas for improvement and implement data-driven, AI-enhanced solutions to boost efficiency and patient care.</li><li>Collaborate with clinicians, healthcare providers, and other stakeholders to ensure clinical content is evidence-based, up-to-date, and aligned with the latest medical guidelines.</li><li>Work closely with the EMR and AI development teams to seamlessly integrate clinical content and intelligent workflows into the software ecosystem.</li><li>Participate in user acceptance testing to ensure clinical content and workflows function as intended within the EMR and AI modules.</li><li>Provide training and support to clinicians and other end-users on effectively utilizing the clinical content and intelligent workflows within the EMR.</li><li>Collaborate with top-tier healthcare professionals and our agile tech team to continuously enhance clinical modules.</li><li>Drive measurable improvements in patient care, decision support, and clinical efficiency through innovative digital health and AI initiatives.</li></ul><div></div><div>
Qualifications:</div><div></div><ul><li>MBBS degree from a HEC Recognized University.</li><li>Familiarity with EMR systems, clinical workflows, and healthcare informatics.</li><li>Knowledge of medical terminologies and coding systems (e.g., ICD-10, CPT, SNOMED CT).</li><li>Experience in clinical research, data analysis, and content development.</li><li>Strong understanding of evidence-based medicine and clinical practice guidelines.</li><li>Excellent analytical and problem-solving skills.</li><li>Strong communication and interpersonal skills to effectively collaborate with cross-functional teams.</li><li>Detail-oriented with a commitment to accuracy and quality.</li><li>Ability to manage multiple projects simultaneously and meet tight deadlines.</li><li>Minimum of 2-3 years of experience in a similar role, preferably in an EMR or healthcare technology setting.</li></ul>
. Familiarity with US Healthcare system is preferred.<div></div><div>
Compensation and Benefits:</div><div><br>
   Financial:</div><div><ul><li><br>
Competitive salary and bi-annual bonus.</li><li>Fast track and uncapped career growth for high performers.</li><li>Company-sponsored vehicle financing (car and bike).</li><li>Interest-free loans.</li><li>Provident Fund: CureMD matches up to 8% of your base salary.</li><li>Fuel Card.</li><li>Cellular Allowance.</li></ul></div><div><br>
   Health and Wellness:</div><div><ul><li><br>
In-house clinic with a team of certified male and female doctors with 24/7 telemedicine service.</li><li>Hospital treatment monitoring by company doctors.</li><li>Comprehensive health coverage for your immediate family (outpatient, inpatient, maternity and parents' inpatient).</li><li>Exclusive health benefits and discounts at top class clinics and labs.</li></ul></div><div><br>
     Supportive Workplace:</div><div><ul><li><br>
Pick-up and drop-off services for female employees.</li><li>In-house daycare facility.</li><li>In-house gym and recreational area to unwind.</li></ul></div><div><br>
   Continued Learning:</div><div><ul><li><br>
Company-sponsored trainings, workshops, development programs and retreats.</li><li>Paid specialized trainings/certifications.</li></ul></div><div></div><div>
The Difference You&rsquo;ll Make:</div><div></div><div>
At CureMD, every role, whether senior or junior, plays a pivotal part in transforming healthcare. By joining our innovative team, you&rsquo;ll contribute to groundbreaking technology that directly impacts patient care, enhances healthcare efficiency, and saves lives globally. Your skills and passion will drive meaningful change, helping us deliver solutions that support healthcare professionals in critical, real-time settings. Together, we&rsquo;re not just advancing technology &mdash; we&rsquo;re making a tangible difference in people&rsquo;s lives. Together, let&rsquo;s save lives.</div></div>

DRK Pharma Solutions

<p><b>Education</b></p><ul><li>PharmD /Bachelor&rsquo;s degree in life sciences from HEC / International Approved University</li></ul><p><b>Experience</b></p><ul><li>2-3 years</li></ul><p><b>Requisites for the Role</b></p><ul><li>Fluency in English.</li><li>Strong spoken and written communication skills, including grammatical/technical writing.</li><li>High proficiency with full Microsoft applications</li></ul><p><b>Roles and Responsibilities </b></p><ul><li>To function as a member of the project team to contribute to the efficient management of trials.</li><li>To negotiate investigator budgets and assist in executing site contracts with support from the legal department.</li><li>To participate in the recruitment of potential Investigators, preparation of Independent Ethics Committee/Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, organization of meetings, and other tasks as directed by the Clinical Research Associate &ndash; III or Lead Clinical Research Associate/Associate Project Lead/Project Lead.</li><li>To communicate with Investigators and other trial staff, ensuring compliance with protocol requirements, local regulations, ICH-GCP, and DRK Pharma Solutions SOPs.</li><li>To conduct initiation visits, training Investigators and trial staff in the protocol and data collection methods to ensure accurate and complete patient data collection.</li><li>To conduct monitoring visits, ensuring adherence to protocol, accurate data collection, and accountability of investigational products/biological samples/supplies.</li><li>To effectively communicate with site personnel, including the Principal Investigator (PI), and DRK management to address protocol/study deviations and implement corrective actions.</li><li>To update the Clinical Study Management System (CSMS) on time.</li><li>To monitor and update data in an Electronic Data Capture (EDC) system according to study guidelines.</li></ul><p><b>Deadline To Apply</b></p><p>November 16, 2025</p><p>Job Type: Full-time</p><p>Pay: From Rs75,000.00 per month</p><p>Work Location: In person</p>

Clinical Research Assistant

My City  Hospital

<p><b>My City Hospital </b>is a trust based, multi-specialty hospital offering all medical services to their patients under one roof, continuously engaged in the serving of humanity with quality care. We are looking for qualified and experienced Doctors for Part time <b>Consultancy services</b> on <b>percentage / sharing </b>basis in <b>different time</b> <b>slots.</b></p><p>Job Types: Part-time, Contract</p><p>Contract length: 12 months</p><p>Expected hours: 2 &ndash; 3 hours per day</p><p><b>Job Title:</b> Consultant Doctor (OPD) - Part-Time</p><p><b>Department:</b> Outpatient / Inpatient Services</p><p><b>Reports To:</b> Hospital Administrator, Medical Director</p><p><b>Job Summary:</b></p><p>This position is for a part-time Consultant Doctor to provide high-quality outpatient medical services to patients within a specified clinic or department. The incumbent will be responsible for patient assessment, diagnosis, treatment planning, and follow-up care.</p><p><b>Key Responsibilities:</b></p><p>1) Patient Care</p><p>2) Clinical Operations</p><p>3) Professional Development</p><p><b>Qualifications:</b></p><p>* Education: MBBS, MCPS / FCPS or equivalent medical degree from a recognized university or CPSP.</p><p>* Licensure/Certification: Valid medical license to practice in the relevant jurisdiction.</p><p>* Experience: 03 years of experience in outpatient clinical settings.</p><p><b>Specialization: </b></p><p><b>1. Sonologist (Female) (Afternoon Timings)</b></p><p><b>2.General Physician (Afternoon Timings)</b></p><p><b>3. Endocrinologist / Diabetologist (Afternoon/Evening Timings)</b></p><p><b>4. Paediatrician / Child Specialist (Afternoon/Evening Timings)</b></p><p><b>5. ENT Specialist (Male) (Afternoon/Evening Timings)</b></p><p><b>6. Neurologist (Female) (Evening Timings)</b></p><p><b>7. Psychiatrist (Afternoon/Evening Timings)</b></p><p><b>8. Dental Surgeon (Male) (Morning Timings)</b></p><p><b>9. Dermatologist (Afternoon/Evening Timings)</b></p><p><b>10.Pulmonologist (Afternoon/Evening Timings)</b></p><p><b>11.Nephrologist (Evening Timings)</b></p><p><b>Skills:</b></p><p>* Excellent communication, interpersonal and patient-centered care skills.</p><p>* Strong diagnostic and clinical judgment skills.</p><p>* Ability to work independently and as part of a multidisciplinary team.</p><p>* Excellent time management and organizational skills.</p><p><b>To Apply:</b></p><p>Interested Doctors may send their resume at <b>info@mycityhospital.pk.</b> May Drop your resume on given below address:</p><p><b>Location: </b>HR Department B-174 Block-5 Karachi Administration Employees Housing Society near Haq Chamber Karachi.</p><p>Job Type: Part-time</p><p>Pay: Rs1,000.00 - Rs5,000.00 per month</p><p>Expected hours: 1 &ndash; 3 per week</p><p>Work Location: In person</p>

CONSULTANT Doctors Required for OPD on PERCENTAGE Basis (Part Time)

Hameed Latif Hospital

<div>
 <p>
  <strong>
   Company Description
  </strong>
 </p>
 <p>
  Hameed Latif Hospital | HLH &ndash; Serve the People provides comprehensive 24-hour emergency services supported by 14 state-of-the-art operation theaters, 2 angioplasty and angiography units, delivery rooms, medical ICUs, neonatal ICUs, and well-equipped clinical indoor departments. The hospital offers specialized care in various fields including cardiac surgery, neurosurgery, neurointervention, orthopaedic surgery, and obstetrics &amp; gynaecology. The hospital features an 8-bed dialysis center, a fully equipped blood bank, advanced diagnostic facilities, and is staffed by over 1000 healthcare professionals to ensure high-quality patient care. Additionally, the hospital provides around-the-clock pharmacy and ambulance services for all patients.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Role Description
  </strong>
 </p>
 <p>
  This is a full-time/ Part-time, on-site role for a Consultant Radiologist based in Lahore. The Consultant Radiologist will be responsible for interpreting medical images such as X-rays, MRIs, CT scans, and ultrasounds, collaborating with physicians and specialists to diagnose patient conditions, and recommending appropriate treatment plans. The Consultant Radiologist will also contribute to the monitoring and improvement of radiology department operations, ensure the accuracy and quality of diagnostic imaging, and participate in case discussions and meetings.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    MBBS, FRCR / FCPS Radiology / Diplomate American Board or Equivalent qualification.
   </strong>
  </li>
  <li>
   Minimum 4-5 years of experience in Radiology Department in a Reputable  hospital or Healthcare Setting.
  </li>
 </ul>
</div>


Consultant Radiologist(Full-time/ Part-Time)

ROZEE.PK

<div><div><div><div><b>1.</b> <b>Purpose
</b></div><div>The objective of this consultancy is to develop a mechanism to revise antimicrobials listed in National Essential Medicines List (NEML) of Pakistan and a Pakistan-specific Access, Watch, Reserve (AWaRe) list of antibiotics in NEML based on the antimicrobial resistance (AMR) and antimicrobial use (AMU) trend. The list will be developed and finalized with the involvement of key stakeholders and accompanied by a practical implementation framework for integration into national antimicrobial governance mechanisms, including prescribing, procurement, stewardship, and regulatory controls..</div><br>
<div></div>
<div><b>
2.</b> <b>Background</b></div>
<div>
AMR is recognized globally and within Pakistan as a critical public health challenge. The WHO&rsquo;s AWaRe classification categorizes antibiotics based on resistance potential, utilization, and spectrum of activity, aiming to guide appropriate antibiotic use. The AWaRe list in low-and-middle income countries (LMICs) guides evidence-based AMR policies in monitoring antibiotic use, regulating over the counter sales and improve prescription-based access to essential antibiotics.
</div><div>The National Institute of Health (NIH) is the National AMR focal point and collects and reports AMR data from sentinel sites, reporting to national and global platforms for evidence-based policies. The Drug Regulatory Authority of Pakistan (DRAP) is AMU focal point to regulate and monitor AMU under national drug regulatory legislation in coordinating with provincial stakeholders.
</div><div>In 2023, DRAP had a consultation with engagement of national experts in the field, and a consultant was engaged to formulate a comprehensive desk review and collect AMR data with the support of NIH from federal and provincial levels, with representation from both the public and private sectors.</div>
<div>
WHO Pakistan is providing technical support to NIH and DRAP for AWaRe classification of antibiotics included in NEML and in the systematic development of Pakistan&rsquo;s first AWaRe list of essential antibiotics with active engagement of stakeholders. The AWaRe list will be used a tool for monitoring antibiotic consumption, defining targets and monitoring the effects of stewardship policies that aim to optimize antibiotic use and curb AMR.</div><br>
<div></div>
<div><b>
3.</b> <b>Work to be performed.</b></div>
<div>
WHO, DRAP and NIH will develop a core group of key stakeholders to oversee the national adaptation and implementation of the WHO AWaRe classification in Pakistan. The consultant will develop an inception report plan and lead the adaptation process, which will involve a contextual review using WHO&rsquo;s methodology, followed by a comprehensive action plan with timeline to integrate the adapted list into Pakistan&rsquo;s health system, through regulatory, prescribing, procurement, and monitoring measures.</div><br>
<div>
</div><div>The consultant is expected to coordinate with WHO, NIH and DRAP focal points team regularly for the refinement and collection of the required information. The methodology will be in alignment with DRAP, NIH guidance for the tasks and approaches mentioned below and consultant will take the lead in reporting against the deliverable.WHO will facilitate a two-day consultation of Technical Working Group (TWG) of relevant experts (federal/provincial) to support national contextualization of the AWaRe classification and guide its integration into the health system through a tailored implementation plan.</div><br>
<div></div>
<div><b>
Output 1: </b><b>Desk review and </b><b>inception report for WHO AWaRe adaptation and implementation planning with timelines.
</b></div><div>l Deliverable 1.1: Conduct a desk review of current global and national guidelines on AWaRe classification. Prepare an inception report detailing the methodology of national adaptation and implementation, with stakeholder mapping and establishing timelines.</div>
<div>
l Deliverable 1.2: Develop a draft AWaRe list adapted to Pakistan&rsquo;s context using the WHO-recommended methodology and available AMR/AMU data, along with comprehensive technical recommendations and guidance for its integration into the health system.</div>
<div>
l Deliverable 1.3: Disseminate the draft list and implementation plan with stakeholders, including DRAP, NIH, and WHO and incorporate their feedback.</div><br>
<div><b>
</b></div><div><b>Output 2: Finalize </b><b>AWaRe list</b><b> through national consultation and </b><b>prepare a comprehensive report</b> <b>with </b><b>clear recommendations and guidelines.</b></div>
<div>
l <b>Deliverable 2.1:</b><b> </b>Conduct an online survey among healthcare professionals across all provinces to get feedback and build consensus on the list.</div>
<div>
l <b>Deliverable 2.2</b><b>:</b> Develop the concept note, agenda and facilitate a two-day Technical Working Group (TWG) consultation with federal and provincial experts, to review the results from survey and review and validate the adapted AWaRe list and incorporate inputs for implementation.
</div><div>l <b>Deliverable 2.3: </b>Finalize the adapted AWaRe list and finalize the comprehensive implementation plan to integrate into Pakistan&rsquo;s health system, covering regulatory alignment, prescribing practices, procurement processes, and monitoring mechanisms based on the TWG consultation.</div>
<div>
l <b>Deliverable 2.3:</b> Submit a report summarising consultative feedback and recommendations.</div><br>
<div>
</div><div><b>4.</b> <b>Technical Supervision</b></div>
<div>
The selected Consultant will work on the supervision of:</div>
<div>
Responsible Officer: Team Lead, HSD</div>
<div>
Manager: Head of WHO Office</div><br>
<div></div>
<div><b>
5.</b> <b>Duration: 30 working days spread over two month.</b></div><br>
<div><b>
</b></div><div><b>6.</b> <b>Specific requirements</b></div>
<div>
Essential qualifications:</div>
<div>
Advanced university degree (Master&rsquo;s level or above) in public health, health systems, microbiology, infectious diseases, medicines, and/or pharmacy sciences.</div><br>
<div></div>
<div>
Experience required (essential): 7 to 10 years of progressive experience in public health, infectious diseases, clinical microbiology, or clinical pharmacy, with demonstrated involvement in antimicrobial stewardship initiatives.</div>
<div>
Experience working with the WHO AWaRe classification system, including its application in hospital or community settings to optimize antibiotic use.</div><br>
<div></div>
<div>
Experience (desirable): Preferably working on patient safety, preferably with work in low- and middle-income countries.</div><br>
<div>
</div><div>Technical skills and knowledge:</div>
<ul>
<li>Demonstrated skills in complex document review, organizational development, and stakeholder engagement including multidisciplinary teams.</li>
<li>Superior editing and analytical skills.</li></ul><br>
<div></div>
<div>
Language requirements:</div>
<div>
Excellent command of both English and the local language.</div><br>
<div></div>
<div><b>
7.</b> <b>Place of assignment:</b> Remote<br>
</div><br>
<br>
</div><div></div><div><h4 class="jobSectionHeader"><b>TOTAL POSITIONS</b></h4>
<p>1</p>
<h4 class="jobSectionHeader"><b>POSTED ON</b></h4>
<p>October 22, 2025</p>
<h4 class="jobSectionHeader"><b>EXPIRY DATE</b></h4>
<p>October 29, 2025</p>
<h4 class="jobSectionHeader"><b>BUSINESS</b></h4>
<p>WHO</p>
<h4 class="jobSectionHeader"><b>CATEGORY</b></h4>
<p>Health &amp; Medicine</p>
<h4 class="jobSectionHeader"><b>JOB TYPE</b></h4>
<p>Consultant</p>
<h4 class="jobSectionHeader"><b>MINIMUM EDUCATION</b></h4>
<p>Masters
</p><h4 class="jobSectionHeader"><b>CAREER LEVEL</b></h4>
<p>Consultant
</p><h4 class="jobSectionHeader"><b>MINIMUM EXPERIENCE</b></h4>
<p>7 Years(Please refer to Job Description section for details)</p></div></div></div>

CONSULTANT (AWARE)

<p><b>Education</b></p><ul><li>Associate degree in Life Sciences</li></ul><p><b>Experience</b></p><ul><li>0-6months</li></ul><p><b>Requisites for the Role</b></p><ul><li>Strong analytical skills</li><li>Basic understanding of clinical trials</li><li>Good documentation management</li><li>Excellent communication</li><li>Resilient and adaptable</li></ul><p><b>Roles and Responsibilities </b></p><ul><li>Perform as a member of the project team with the goal to contribute towards efficient management of trials.</li><li>Communicates effectively with site personnel and DRK supervisor to update the study tracker with latest study status.</li><li>To update the study tracker with latest safety updates from allocated sites.</li><li>Liaises with site to resolve data discrepancies and ensures all study goals are met as per supervisor&rsquo;s instruction.</li><li>Initiates payment requests for investigators (If required).</li><li>Performs other duties as assigned by management.</li><li>Logistics support to CRM and CRAs.</li><li>Maintain the study files as per supervisor&rsquo;s instructions.</li><li>Assist with the preparation, distribution, and tracking of study documents such as protocols, informed consent forms, investigator brochures, and study manuals. Maintain Trial Master File (TMF) and ensure completeness and audit readiness according to SOPs and ICH-GCP guidelines.</li><li>Support site start-up activities, including collection and review of essential documents and coordinating ethics submissions.</li><li>Schedule and coordinate meetings, prepare agendas, take minutes, and track action items.</li><li>Update and maintain clinical trial management systems (CTMS), electronic Trial Master File (eTMF), and other study databases.</li><li>Assist in the tracking of study metrics, enrollment, and timelines.</li><li>Liaise with clinical research associates (CRAs), sites, and vendors to ensure timely communication and resolution of issues.</li><li>Support clinical supply management, including tracking and distribution of investigational product (IP) and study materials.</li><li>Assist in preparation for audits and regulatory inspections</li><li>Perform other duties as assigned by management.</li></ul><p><b>Deadline To Apply</b></p><p>November 30 , 2025</p><p>Job Type: Full-time</p><p>Pay: From Rs45,000.00 per month</p><p>Work Location: In person</p>

Clinical Trial Assistant

Explore 529+ Associate clinical consultant in Pakistan this November. Find roles across top companies and apply now to boost your career.

529 associate clinical consultant jobs IN Pakistan

Associate Clinical Consultant

Associate Clinical Consultant

Clinical Research Assistant

CONSULTANT Doctors Required for OPD on PERCENTAGE Basis (Part Time)

Consultant Radiologist(Full-time/ Part-Time)

CONSULTANT (AWARE)

Clinical Trial Assistant