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research associate

Aga Khan University

<div><div>Research Associate, Department of Oncology - (250002XW)</div><div><div><br>
</div><p><b>Introduction:</b></p><p>
The Aga Khan University was founded in 1983 as Pakistan&rsquo;s first private university, Aga Khan University is a not-for-profit institution and an agency of the Aga Khan Development Network. Starting in 2000, the University expanded to Kenya, Tanzania, Uganda, United Kingdom and Afghanistan. AKU began life as a health-sciences university.</p><p>
The Department of Oncology offers comprehensive cancer care services to all patients. The services are provided through multidisciplinary teams. Infrastructure facilities include a daycare setting dedicated to oncology patients. Outpatient facilities include clinics of Medical, Hematology, Paediatric, Radiation, and Palliative Care.</p><p>
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.</p><p>
Aga Khan University invites applications for the position of Research Associate, Department of Oncology.</p><p><b>
Responsibilities:</b></p><p>
You will be responsible to:</p><ul><li>
provide assistance and support in organising departmental events i.e. conferences/ workshops/ courses/symposium</li><li>
providing assistance to various departmental committees</li><li>
work with other department team members and other stakeholders i.e. Food Services, Finance, Purchase etc</li><li>
organize National and International tumor boards</li><li>
develop and maintain a strategy for clinical, education, fellowship and research related information and activities in the Department of oncology</li><li>
prepare and editing documents for presentation, SPSS and publications and disseminate the same to the stakeholders</li><li>
take continuous follow-ups from the support departments for ensuring the completeness of work on time</li><li>
prepare budget sheets and maintain the GVR for grants</li><li>
take continuous follow-ups from the support departments for ensuring the completeness of work on time</li><li>
make presentations on behalf of the Department, as and when required</li><li>
play a role in research audit and maintaining files and play role in all the quality certifications (ISO, JCIA certification/accreditation) in order to align with the institutional vision/mission</li><li>
review the literature related to assigned topic</li><li>
review the case history of the identified individuals</li><li>
assist in proposal development &amp; manuscript writing</li><li>
perform primary data collection, analyses of data and writing up results</li><li>
conduct assigned qualitative and quantitative analysis</li><li>
prepare weekly and monthly progress report</li><li>
schedule, coordinate and organize the Weekly or Monthly Tumor Boards.</li></ul></div><div></div><div><div><br>
</div><p><b>Requirements:</b></p><p>
You should have:</p><ul><li>
an MBBS degree</li><li>
knowledge and experience related to research will be preferred</li><li>
knowledge and interest in the field of specialty</li><li>
demonstrated skills in data collection and analysis</li><li>
strong academic and scientific writing skills</li><li>
proficiency in use of computer applications</li><li>
good interpersonal skills and communication skills</li><li>
interested in pursuing a career in Pediatric Neuro-oncology and Public Health</li><li>
excellent written and verbal communication skills with ability to plan and execute process improvements related to work management</li><li>
ability to handle correspondence and other assignments independently without being micromanaged</li><li>
strong interpersonal skills.</li></ul><p>
*Comprehensive employment reference checks will be conducted*</p><div><br>
</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: 10/10/2025, 6:38:23 AM</div><div>
Closing Date: 24/10/2025, 1:59:00 PM</div></div>

Research Associate, Department of Oncology

<div><div>Research Associate (Statistician), Paediatrics &amp; Child Health - (2500032Q)</div><div><div><br>
</div><p><b>Introduction:</b></p><p>
The Outreach and Research Programme of the Department of Paediatrics and Child Health has ten community-based field sites across Pakistan (including four in Karachi) and focuses on research for betterment of women and child health. The Department has a Nutritional Research Laboratory as well as an Infectious Disease Research Laboratory that cater to the needs of its research projects. It has well-acclaimed work to its credit both at the national and international level.</p><p>
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.</p><p><b>
Responsibilities:</b></p><p>
You will be responsible to analyse and interpret data from research projects; prepare descriptive tables; check data for inaccuracies; data cleaning and management and report results of statistical analyses. Specific responsibilities will be to:</p><ul><li><div>
provide statistical and analytical support to the research team</div></li><li><div>
coordinate with the project teams and independently manage all complex statistical aspects of research</div></li><li><div>
projects.</div></li><li><div>
analyze and evaluate statistical results, prepare derived datasets for the analysis using statistical</div></li><li><div>
packages like Stata, R and python</div></li><li><div>
provide Expertise in data management, data mining and prepare statistical reports with interpretation</div><div>
for manuscript publications.</div></li><li><div>
collaborate with funding agencies such as WHO and BMGF on analysis of multi-site studies</div></li><li><div>
prepare statistical contribution to Integrated Study Report;</div></li><li><div>
develop project analysis plan, including computer-generated table specifications, statistical analysis</div></li><li><div>
plan, and research report format;</div></li><li><div>
use statistical techniques and models to forecast results, trends and needs;</div></li><li><div>
prepare project summaries for weekly/monthly status meetings;</div></li><li><div>
prepare any other official assignments given by the supervisor(s)</div></li><li><div>
analyse and interpret data from research projects and prepare descriptive tables;</div></li><li><div>
check data for inaccuracies, Data Cleaning &amp; Management;</div></li><li><div>
report results of statistical analyses, including information in the form of graphs, charts, and tables;Requirements.</div></li></ul></div><div></div><div><div><br>
</div><p><b>Requirements:</b></p><p>
You should have:</p><ul><li><div>
minimum 1-2 years of experience;</div></li><li><div>
experience in the field of Research &amp; public health will be an added advantage</div></li><li><div>
4 years graduation or Masters in Statistics</div></li><li><div>
excellent Command on SPSS/Stata and other Statistical Packages;</div></li><li><div>
proficient in Spread sheets and power point presentation;</div></li><li><div>
sound knowledge of Databases and programming;</div></li><li><div>
strong verbal and written communication skills.</div></li></ul><p>
Comprehensive employment reference checks will be conducted.</p><p><b>
Disclaimer:</b></p><p>
The Aga Khan University is committed to the principles of equal employment opportunity for all employees and to providing employees with a work environment which is free from discrimination and harassment. All employment decisions at AKU are based on business needs, job requirements and individual&rsquo;s qualifications and experience, without regard to race, colour, caste or creed, national, social or ethnic origin, gender (except where gender is a bona fide occupational qualification). AKU does not discriminate among the job candidates on account of any of these characteristics.</p><div><br>
</div></div><div>
Primary Location: Pakistan-Karachi</div><div>
Organisation: Aga Khan University Pakistan</div><div>
Employee Status: Contractual</div><div>
Job Type: Experienced</div><div>
Job Posting: 24/10/2025, 4:48:30 AM</div><div>
Closing Date: 31/10/2025, 1:59:00 PM</div></div>

Research Associate (Statistician), Paediatrics & Child Health

<div><div>Research Associate, Paediatrics &amp; Child Health -MC - (2500032M)</div><div><div><br>
</div><p><b>Introduction:</b></p><p>
The Outreach and Research Programme of the Department of Paediatrics and Child Health has ten community-based field sites across Pakistan (including four in Karachi) and focuses on research for betterment of women and child health. The Department has a Nutritional Research Laboratory as well as an Infectious Disease Research Laboratory that cater to the needs of its research projects. It has well-acclaimed work to its credit both at the national and international level.</p><p>
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.</p><p><b>
Responsibilities:</b></p><p>
You will be responsible to supervise all project related activities from field management to data collection, quality control of data collection and maintain good working relationship among staff &amp; community. Specific responsibilities will be to:</p><ul><li><div>
monitor the data collection process in the field, evaluating and ensuring the accuracy of the data</div></li><li><div>
write a weekly report</div></li><li><div>
coordinate with the project supervisors to discuss field related activities</div></li><li><div>
provide training to the staff as per the protocols and guidelines of study</div></li><li><div>
oversee the project, simultaneously, ensuring smooth and efficient day-to-day operation of research related activities</div></li><li><div>
ensure all research related auditable materials are always up to date</div></li><li><div>
conduct In depth interviews and FGDs</div></li><li><div>
monitor all components of the project in the field, evaluating, and ensuring the accuracy of the data.</div></li><li><div>
translate and transcription of data from Urdu to English.</div></li></ul></div><div></div><div><div><br>
</div><p><b>Requirements:</b></p><p>
You should have:</p><ul><li><div>
Master&rsquo;s or equivalent or MBBS background will be preferred</div></li><li><div>
one &ndash; two years of relevant work experience</div></li><li><div>
strong communication and interpersonal skills</div></li><li><div>
team player.</div></li><li><div>
good writing skills.</div></li><li><div>
basic Knowledge of survey and other research designs</div></li><li><div>
data collection, analysis and interpretation in terms of report writing and biostatics</div></li><li><div>
strong interpersonal skills and communication</div></li><li><div>
integrity and strong research ethics;</div></li><li><div>
excellent written and verbal communication skills in English;</div></li><li><div>
comfort with working in challenging field-based settings.</div></li><li><div>
proven mixed methods research skills;</div></li><li><div>
strong people management skills, particularly in challenging field environment</div></li></ul><p>
Comprehensive employment reference checks will be conducted.</p><p><b>
Disclaimer:</b></p><p>
The Aga Khan University is committed to the principles of equal employment opportunity for all employees and to providing employees with a work environment which is free from discrimination and harassment. All employment decisions at AKU are based on business needs, job requirements and individual&rsquo;s qualifications and experience, without regard to race, colour, caste or creed, national, social or ethnic origin, gender (except where gender is a bona fide occupational qualification). AKU does not discriminate among the job candidates on account of any of these characteristics.</p><p></p><div><br>
</div></div><div>
Primary Location: Pakistan-Karachi</div><div>
Organisation: Aga Khan University Pakistan</div><div>
Employee Status: Contractual</div><div>
Job Type: Experienced</div><div>
Job Posting: 24/10/2025, 1:07:01 AM</div><div>
Closing Date: 31/10/2025, 1:59:00 PM</div></div>

Research Associate, Paediatrics & Child Health -MC

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

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>TuBXaWOaue</p></div>

Clinical Trials Quality Assurance Associate (Night)

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


TECHNEXIA

<p>Technexia is a full-service digital agency where data meets creativity. We're looking for a Research Analyst with strong academic writing and analytical skills to support research-driven projects across various domains.</p><p>Responsibilities :</p><p>* Conduct in-depth literature reviews &amp; data collection.</p><p>* Write structured, clear academic reports and technical papers.</p><p>* Analyze data using tools like SPSS, R, or Python.</p><p>* Design methodologies for surveys, case studies, or experiments.</p><p>* Ensure academic integrity and proper referencing (APA/MLA/Chicago)</p><p>Requirements :</p><p>* Experience in academic/technical writing.</p><p>* Proficiency in research tools and statistical analysis.</p><p>* A Bachelors or Master&rsquo;s degree in a related field such as Biotechnology, Biomedical Physics, Engineering, Social Sciences, Literature, or any other relevant domain.</p><p>* 6 Months to 2 years research or publication experience is a plus.</p><p>Timings : 8:30 AM to 4:30 PM</p><p>Type: Full-time (in-house)</p><p>Apply: people@technexia.com</p><p>Location: Block-F, North Nazimabad - opposite to the North Walk Karachi.</p><p>https://lnkd.in/dJwEskSj</p><p>Job Type: Full-time</p><p>Pay: Rs40,000.00 - Rs70,000.00 per month</p><p>Work Location: In person</p>

Research Analyst

Explore 466+ Research associate in Karachi this October. Find roles across top companies and apply now to boost your career.

466 research associate jobs IN Karachi

Research Associate, Department of Oncology

Research Associate (Statistician), Paediatrics & Child Health

Research Associate, Paediatrics & Child Health -MC

Clinical Research Assistant

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

Research Analyst