9 Research Coordinator jobs in Pakistan

We are seeking a Research & Support Analyst to join our team. To be successful in this position, you’ll be a self-starter, capable of delivering brilliant creative ideas, and show amazing attention to detail. We are looking for an individual with experience in record keeping, timesheet and data entry. Key Responsibilities

Carrier company invoices are reviewed in detail. Collect the relevant information, such as BOL number, Pro Numbers, Consignee, and consigner. Process them within the client-directed transaction time. Mark them and assign notations as per each job description. Currently working with over 200+ CASS clients and carriers. Learning the procedures and keeping up to date with fresh product knowledge. Skills & Abilities

Typing: 30-40 WPM Excellent presentation and communication skills regarding technical and non-technical concepts. Strong initiative and self-awareness – a flexible team player. Creative thinker. Demonstrated strength in employee communication. Program planning and facilitation experience. Experience driving engagement, and building and implementing related programs. Requirements

Minimum graduate from a recognized university. Previous experience in the BPO industry. Minimum of 2+ years of experience with data handling and invoice reading capabilities. Strong computer skills including Excel are required. Must be comfortable using filters and tables in Excel. Self-starter and comfortable working in a fast-paced dynamic environment. Strong attention to detail, adaptability, and being very organized. Must have excellent communication, strong interpersonal and problem-solving skills, with the ability to build friendly and collaborative working relationships with clients and colleagues. Must be fluent in English both oral and written. Preferable experience with US Clients. What We Offer

Market Competitive Salary Career Growth Learning & Development Provident Fund EOBI Paid Leaves Life Insurance Location:

NASTP, Lahore Timing:

05:30am – 02:30pm

#J-18808-Ljbffr

At least Bachelor Degree (Any Discipline)

MULTIPLE CANDIDATES ARE REQUIRED. Work for a US based company.
Excellent Growth and Learning Opportunities for the right candidates.

Job Description:

We are looking for a highly motivated and organized individual to work as a research associate, data analyst, Digital Marketing associate and Lead Coordinator for real estate businesses.

Qualifications / Skills:

1. Display excellent skills in internet research, data analysis, preparing excel/word reports and making it presentable.
2. Willingness to learn new tools, systems and technologies.
3. Good understanding of social media marketing and campaigns.
4. Show good organizational and time management skills.
5. Strong teamwork skills.
6. A bachelor's degree (in any discipline) is preferred.
7. Willing to work in evening shifts.

Job Type: Full-time
Job Location: Lahore
Timing: Evening to night Shift
Required Education: At least Bachelor Degree (Any Discipline)

Interested candidates should send their resume at and mention in subject "Real Estate Research Associate/ Digital Marketing Associate/ Data Analyst or Lead Coordinator"

Job Specification Responsibilities:

1. Perform internet research, data analysis, preparing excel/word reports and making it presentable.
2. Manage leads, follow ups, generate offers, manage contracts and take leads to closure.
3. Excellent writing skills to help in process documentation.
4. Good command on using internet/online tools to research and produce content related to real estate processes.
5. Keep track of completed tasks and goals to measure lead conversion ratio and meet performance benchmarks.
6. Daily updates to client with feedback and progress reports.
7. Monitor project progress and handle any issues that arise during process support.

#J-18808-Ljbffr

At least Bachelor Degree (Any Discipline) MULTIPLE CANDIDATES ARE REQUIRED. Work for a US based company. Excellent Growth and Learning Opportunities for the right candidates. Job Description:

We are looking for a highly motivated and organized individual to work as a research associate, data analyst, Digital Marketing associate and Lead Coordinator for real estate businesses. Qualifications / Skills:

Display excellent skills in internet research, data analysis, preparing excel/word reports and making it presentable. Willingness to learn new tools, systems and technologies. Good understanding of social media marketing and campaigns. Show good organizational and time management skills. Strong teamwork skills. A bachelor's degree (in any discipline) is preferred. Willing to work in evening shifts. Job Type: Full-time Job Location: Lahore Timing: Evening to night Shift Required Education: At least Bachelor Degree (Any Discipline) Interested candidates should send their resume at and mention in subject "Real Estate Research Associate/ Digital Marketing Associate/ Data Analyst or Lead Coordinator" Job Specification

Responsibilities:

Perform internet research, data analysis, preparing excel/word reports and making it presentable. Manage leads, follow ups, generate offers, manage contracts and take leads to closure. Excellent writing skills to help in process documentation. Good command on using internet/online tools to research and produce content related to real estate processes. Keep track of completed tasks and goals to measure lead conversion ratio and meet performance benchmarks. Daily updates to client with feedback and progress reports. Monitor project progress and handle any issues that arise during process support.

#J-18808-Ljbffr

Research Associate, Short Term Support Staff Department of Nutritional Science

Applications are invited from Pakistani Nationals, who are not married to a foreign national, for the position in the Department of Food Science under HEC project No. 20-116348/NRPU/R&D/HEC/2021, titled “Potential utilization and value addition of pomegranate peel extract by exploring its therapeutic and antimicrobial potential in bakery products” .

Post Name: Research Associate (1)

Number of Positions: 1

Honorarium: Rs. 11,666/month

Contract Duration: 1 year (extendable)

Qualifications: B.Sc. (Hons.)/BS or equivalent in Nutritional Sciences or relevant field

Experience: Preference for candidates enrolled in MS-HND with knowledge of physicochemical analyses and report writing. Responsibilities include field and lab work, raw material collection, chemical analyses, report and proposal writing, and manuscript preparation.

Post Name: Short Term Support Staff (1)

Number of Positions: 1

Honorarium: Rs. 12,500/month

Contract Duration: 1 year (extendable)

Qualifications: B.Sc. (Hons.)/BS or equivalent in Nutritional Sciences or relevant field

Experience: Candidates with relevant working experience in physicochemical analyses and report writing. Responsibilities include laboratory and field work, chemical analyses, report and manuscript writing.

The project duration is 24 months. Positions are temporary, and incumbents will sign a bond for the project duration.

How to apply: Submit a one-page application with a short CV to the Principal Investigator at the Department of Nutritional Sciences, GCU Faisalabad, by January 18, 2024 .

Dr. Aftab Ahmed
Principal Investigator
HEC project 16348/NRPU/R&D/HEC/2021
Associate Professor
Department of Nutritional Science
Government College University, Faisalabad

#J-18808-Ljbffr

Clinical Research Manager
BioVance Research International, Pakistan

BioVance Research International is seeking Clinical Research Monitors.

The designee will be responsible for managing the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Plans, oversees, and executes bioequivalence studies and PK studies. Oversees adherence to SOPs, Good Clinical Practice, and FDA/MHRA/EMA regulations.

The position reports directly to top management.

Package

Attractive gross salary offered.
Plus company medical scheme for self and family, company maintained car, and mobile SIM with monthly limit (all benefits after confirmation).
Probationary period: 3 months.

Job Specification

Requires a master's degree or PhD and at least 5 years of experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures. Will need to rely on extensive experience and judgment to plan and accomplish goals. A degree of creativity and latitude is required and expected. Will perform a variety of tasks and lead and direct the work of others.

Information Technology and Services - Karachi, Pakistan

#J-18808-Ljbffr

Clinical Research Manager BioVance Research International, Pakistan

BioVance Research International is seeking Clinical Research Monitors.

The designee will be responsible for managing the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Plans, oversees, and executes bioequivalence studies and PK studies. Oversees adherence to SOPs, Good Clinical Practice, and FDA/MHRA/EMA regulations.

The position reports directly to top management. Package

Attractive gross salary offered. Plus company medical scheme for self and family, company maintained car, and mobile SIM with monthly limit (all benefits after confirmation). Probationary period: 3 months. Job Specification

Requires a master's degree or PhD and at least 5 years of experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures. Will need to rely on extensive experience and judgment to plan and accomplish goals. A degree of creativity and latitude is required and expected. Will perform a variety of tasks and lead and direct the work of others. Information Technology and Services - Karachi, Pakistan

#J-18808-Ljbffr

Research Associate, Clinical Trials Unit Entity

Medical College

Location Introduction

Aga Khan University was established in 1983 as an international university with an objective to promote human welfare in general, and the welfare of the people in the countries in which it operates, by disseminating knowledge and providing instruction, training, research and service in the health sciences, education and such other branches of learning as the University may determine.

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 & internationally. The Department promotes AKU’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:

• liaise and coordinate study requirements with relevant units and departments of the institution, in line with AKU institutional policies
• organize and/or administer the informed consent process in conjunction with the Principal Investigator
• coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures
• disburse investigational product upon written authorization from the PI and provide relevant teaching with respect to its administration
• maintain study documentation as per protocol and GCP requirements (screening, subject recruitment, investigational drug accountability, enrolment, monitoring and study visit, adverse/serious adverse events etc.)
• review/monitor patients for changes such as in health status, response to investigational product, adverse events, compliance in use of investigational product, concomitant medication use, protocol compliance
• provide laboratory support services including phlebotomy and collection/handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques
• review clinical trials protocols and shared feedback with supervisors for approval
• facilitate internal and external audits of the unit
• draft and report SAE, annual/periodic reports to regulatory bodies and sponsor

Requirements

You should have:

• a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field
• must have a current registration & be in good standing with their professional association
• at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other
• possess excellent clinical skills
• ability to work in independently and versatility to work in a variety of roles
• excellent written and verbal communication skills in English
• integrity and strong research ethics
• efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel).

• a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field
• must have a current registration & be in good standing with their professional association
• at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other
• possess excellent clinical skills
• ability to work in independently and versatility to work in a variety of roles
• excellent written and verbal communication skills in English
• integrity and strong research ethics
• efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel).

Comprehensive employment reference checks will be conducted.To Apply

Interested candidates should send their detailed CVs to and mark the subject line with position number "10011569".

Only shortlisted candidates will be contacted.

Applications should be submitted latest by September 16, 2024

#J-18808-Ljbffr

Research Associate, Clinical Trials Unit

Entity

Medical College Location

Introduction

Aga Khan University was established in 1983 as an international university with an objective to promote human welfare in general, and the welfare of the people in the countries in which it operates, by disseminating knowledge and providing instruction, training, research and service in the health sciences, education and such other branches of learning as the University may determine. 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 & internationally. The Department promotes AKU’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: liaise and coordinate study requirements with relevant units and departments of the institution, in line with AKU institutional policies organize and/or administer the informed consent process in conjunction with the Principal Investigator coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures disburse investigational product upon written authorization from the PI and provide relevant teaching with respect to its administration maintain study documentation as per protocol and GCP requirements (screening, subject recruitment, investigational drug accountability, enrolment, monitoring and study visit, adverse/serious adverse events etc.) review/monitor patients for changes such as in health status, response to investigational product, adverse events, compliance in use of investigational product, concomitant medication use, protocol compliance provide laboratory support services including phlebotomy and collection/handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques review clinical trials protocols and shared feedback with supervisors for approval facilitate internal and external audits of the unit draft and report SAE, annual/periodic reports to regulatory bodies and sponsor Requirements

You should have: a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). Comprehensive employment reference checks will be conducted. To Apply

Interested candidates should send their detailed CVs to and mark the subject line with position number "10011569". Only shortlisted candidates will be contacted. Applications should be submitted latest by

September 16, 2024

#J-18808-Ljbffr