126 Clinical Supply jobs in Pakistan

JOB DESCRIPTION:

Minerva Research Solutions is a clinical trial management service provider.We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.

We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.

Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data. Responsibilities: Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness. Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations. Perform quality control checks; identify and track source documentation errors and non-conformances with requirements. Provide ongoing compliance support including but not limited to: 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. 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). Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities. Assist in preparing for all Sponsor and FDA audits. Assist in conducting internal audits to review key processes. Provide appropriate support to assigned cross-functional workgroups. 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. Query resolution and data entry and questionnaire preparation regarding the respective studies. Other related Quality Assurance projects as assigned. The QA Associate will report to the Quality Assurance Lead Knowledge, Education, and Experience: Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc)with a keen interest in Clinical Research are strongly encouraged to apply. In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials. Knowledge of IRB requirements. 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred. Experience including external clinical/regulatory and document auditing will be a plus Skills and Abilities: Good communication skills (interpersonal, written, verbal) Strong attention to detail and good time management skills Flexible attitude concerning work assignments Ability to manage multiple and varied tasks in a fast-moving environment Ability to interact professionally at all levels within the organization. Knowledge of the HIPAA Privacy Act and its application to clinical research. Benefits:

Competitive salary and performance-based bonuses. Medical health insurance coverage. Employees Old-age benefits coverage. Flexible work hours and remote work options. Professional learning and developmentsupport. Generous vacation and paid time off. Employee assistance programs for mental health. Company-sponsored events and team-building activities. Diverse, professional, and inclusive work environment. Opportunities for career growth. Cutting-edge technology and tools. Family-friendly policies, including parental leave. Commuter benefits or transportation assistance. Social responsibility and community involvement programs. Openings:

04 positions Full-time On-site job

Work Schedule Timings: Monday to Friday Evening Shift (06 PM to 02 AM) (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)

#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

This is a full-time, on-site role for a Supply Chain Director located in Lahore. The Supply Chain Director will be responsible for overseeing and managing the entire supply chain process, including procurement, production planning, and supply chain operations. The role involves analyzing and optimizing supply chain strategies to enhance efficiency and reduce costs, as well as ensuring timely delivery of products and services.

Company Description

We suggest you enter details here

Role Description

This is a full-time, on-site role for a Supply Chain Director located in Lahore. The Supply Chain Director will be responsible for overseeing and managing the entire supply chain process, including procurement, production planning, and supply chain operations. The role involves analyzing and optimizing supply chain strategies to enhance efficiency and reduce costs, as well as ensuring timely delivery of products and services.

Qualifications

• Experience in supply chain management and operations
• Skills in procurement and production planning
• Strong analytical skills for analyzing and optimizing supply chain processes
• Excellent leadership and decision-making abilities
• Effective communication and interpersonal skills
• Ability to work collaboratively with cross-functional teams
• Proven track record in managing and leading supply chain teams
• Bachelor's degree in Supply Chain Management, Business Administration, or related field

Seniority level

• Seniority level Director

Employment type

• Employment type Full-time

Job function

• Job function Management and Manufacturing
• Industries Industrial Machinery Manufacturing

Referrals increase your chances of interviewing at Dkn4Engineering by 2x

Sign in to set job alerts for “Supply Chain Director” roles.

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

#J-18808-Ljbffr

Are you an effective and passionate communicator with the drive to succeed? If so, this is a great opportunity for you to join our growing team.
We are expanding the business globally, you will help us to manage our customer’s supply chains.
This is your opportunity work at innovative and growing business. Our procurement division in Pakistan is a key for our growth plan to offer a high level of service to both existing and new clients.

Key Responsibilities:

1. Communicate closely with your internal customers (sales, engineering, project management etc.), ensure the quotation enquiry and purchase request can be efficiently transferred into PO, and track the PO to ensure on time delivery to meet our overseas manufacturing plan.
2. Communicate closely with overseas suppliers to maintain communication channels for technical information sharing, quotation negotiation and purchase order tracking, ensure clear understanding of what is in the demand pipeline from technical, timeline and cost target aspects.
3. Implementing a proactive risk management approach to prevent delivery delay, cost overcharges and quality non-conformance and understand the importance of seeking support before issues cause irreversible consequences.
4. Be on the search for new suppliers through different ways to prepare for potential future business demand.

Requirements:

1. Have 3 to 5 years working experience in a manufacturing company, covering the responsibility of sourcing or procurement, fan industry or related ones would be an advantage.
2. Proficient in ways to look for suppliers globally and evaluate their capability to fulfill our demand.
3. Understand the normal workflow within a factory from receiving sales order, planning, purchasing, manufacturing, quality assurance to final delivery to customer.
4. Have the skills for cost analysis and negotiation.
5. Ability to use MS Suite (Excel & Word), ERP (SAP) user experience would be an advantage.
6. Excellent English written and spoken skills are mandatory.
7. Bachelors degree in supply chain or related area is preferred.

Wh y join Greybeard?

1. Market competitive salary
2. International client’s exposure
3. Access to state-of-the-art tools and technologies
4. Positive work culture & collaborative environment
5. Team building activities.
6. Competitive compensation & benefits.

Benefits:

1. Educational Assistance
2. Medical Insurance
3. Life Insurance
4. EOBI
5. Off day Working
6. Much More.
   

#J-18808-Ljbffr

Get AI-powered advice on this job and more exclusive features.

Brand Edge Marketing is an integrated marketing agency dedicated to giving your brand a competitive edge required to succeed in the marketplace. We combine cutting-edge technology and creativity to create breakthrough experiences that engage audiences, delivering unprecedented value on your marketing investments.

Role Description

This is a full-time, on-site role for a Supply Chain Manager located in Karāchi. The Supply Chain Manager's responsibilities include coordinating and managing all activities related to supply chain operations. Daily tasks involve demand planning, overseeing inventory management, and procurement processes to ensure timely delivery and supply availability. Additionally, the role requires analyzing supply chain data and performance to enhance efficiency and reduce costs.

Qualifications

• Skills in Demand Planning and Supply Management
• Strong Analytical Skills
• Proficiency in Inventory Management
• Experience in Procurement
• Excellent organizational and problem-solving skills
• Ability to work effectively in a team environment
• Experience in the marketing industry is a plus
• Bachelor's degree in Supply Chain Management, Business Administration, or related field

Apply at

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Management and Manufacturing

Industries

• Advertising Services

Referrals increase your chances of interviewing at Brand Edge Marketing by 2x

Sign in to set job alerts for “Supply Chain Manager” roles.

Karachi Division, Sindh, Pakistan 2 days ago

Karachi Division, Sindh, Pakistan 4 months ago

Karachi Division, Sindh, Pakistan 4 months ago

Karachi Division, Sindh, Pakistan 2 months ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

#J-18808-Ljbffr

- Experience in supply chain management functions.

- The job will involve identifying, selecting, and building relationships with potential suppliers beneficial to the company.

- Conducting data analyses, cost analyses, and other value chain analyses for cost reduction and margin improvement.

- Sourcing and developing import products on a product-wise basis.

- Managing and overseeing overall supply chain operations.

- Making recommendations to improve productivity, quality, and efficiency of supply chain operations.

Job Specification

Candidate must have 3 to 4 years of experience in all functions of supply chain management.

Location: Information Technology and Services - Karachi, Pakistan

#J-18808-Ljbffr

1.Develop the system of supply chain in shape of proper policies, procedures and relevant supporting documents for all the sub-domains of supply chain department which can be use for ERP Development.
2.Plans and implements activities related to the timely, cost-effective inventory control
3.Establish proper vendor selection criteria and Make sure the procurement is being made through suppliers who have cleared the company established vendor selection criteria.
4.Ensure that inventory is managed through proper KAIZEN Management System and proper inventory levels are maintained.
5.Assist top management in forecasting and planning of production and assign the production targets (as per orders) to Dy. Production Manager.
6.Get report on Production from Dy. Production Manager in order to make sure the on time delivery of produced goods for further processing.
7.Make Sure that the finished goods are order wise delivered to destination with a proper coordination of warehouse and export department.
8.Ensure 100% Quality Assurance of products by actively supervising the QA staff.
9.Actively conduct unannounced internal meetings with the divisional Incharges in Supply chain department.
10.As a line manager, responsible to manage all the staff issues of Supply Chain Department.
11.Quarterly perform the performance appraisal of immediate staff with the support of HR Department
12.Any other tasks related to Supply Chain assigned by Top Management.

Job Specification

Qualification: BBA / MBA (majors in Supply Chain) with Diploma in Supply Chain Management or any Master Level Degree in Supply Chain.
Experience: 5 to 6 Years
Skills: Analytical & Managerial
Ability to interface with all levels of internal management and supplier management
Strong analytical abilities and ability to plan, control and direct activities and resources related to planning and scheduling
Strong presentation and organizational skills

Management Consulting - Lahore, Pakistan

#J-18808-Ljbffr

Setting up and managing international supply chains. Development of collaborative relationships with international partners.

Job Specification

Minimum BSc in Engineering along with a Master's Degree. 5+ years experience in Supply Chain Management. Must have experience in setting up and managing international supply chains. Broad business background, with experience in an automotive or engineering business. Experience in the development of collaborative relationships with international partners. Must be able to travel nationally and internationally as required.

Information Technology and Services - Lahore, Pakistan

About Us

Welcome to AEDesign, the premier engineering design and consultancy company in Pakistan. We specialise in engineering and analytical services for the mass automotive and industrial machine industries.

#J-18808-Ljbffr