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Tuesday, October 11, 2022

[New post] Pfizer Hiring for Clinical Research Laboratory /Senior Analytical Technician

Site logo image SWARNALATHA B posted: " Pfizer Hiring 2022. Pfizer Notification full details below. Interested and eligible candidates can Apply Now.Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential t" Pharma Job Alert

Pfizer Hiring for Clinical Research Laboratory /Senior Analytical Technician

SWARNALATHA B

Oct 12

Pfizer Hiring 2022. Pfizer Notification full details below. Interested and eligible candidates can Apply Now.Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place. 

Vacancy details:

  • Post Name: Clinical Research Laboratory /Senior Analytical Technician
  • Qualification: Minimum of a Diploma/Bachelor degree Medical Biology or equivalently
  • Experienced: Excellent communication skills Minimum of 3 years of Laboratory experience

Job Description: Greeting from Pfizer !!!!

Important Details :

  • Post of date:12/10/2022
  • Location: Belgium - Anderlecht
  • Selection Process: The selection will be on the basis of Interview.

Roles and Responsibilities

Your responsibilities:

  • The Clinical Research Laboratory Senior analytical Technician's main responsibility includes proper sample management, storage and all analytical work  on a day-to-day level.
  • Involved in different various activities in the laboratory.
  • Training of new colleagues and updating the training materials
  • Inventory management and controls for the laboratory
  • Optimize Operational Control and Effectiveness
  • Fosters positive community attitudes and volunteer trust through professional behavior and ongoing communication.

The Clinical Research Laboratory Senior Technician is responsible for the day-to-day Laboratory work.

  • Ensure the control of the laboratory environment, safety specification, the maintenance and calibration of laboratory material required to conduct clinical trials.
  • Responsible for orders of the laboratory (identification of supplier, making contact, order tracking, …)
  • Must be able to follow written and oral instructions and comply with safety and laboratory procedures.
  • Creation/review and update SOP's of the laboratory when it is necessary

Sample Management

  • Responsible to ensurequality throughout sample processes and beyond
  • Manage all necessary preparations in regard to the laboratory for adequate execution of a protocol in a timely manner
  • Ensure proper lab samples handling (documents for staff use: trolley sheet, centrifugation sheet, urine collection sheet, order Lab supplies, etc…)
  • Support setting up of EDCMS as appropriate
  • Ensure proper inventory management in Eworkbook

Analytical

  • Perform all routine and special clinical chemistry, hematological, coagulation, and urinalysis, immunological and other tests according to the Standard Operating Procedures.
  • Implement and validate new assays. May assist with assay development. Coordinates with the guidance of the Managers new methods validation and instruments implementation.
  • Perform all quality control checks (monitor trends) on instruments, reagents, and techniques, maintain quality control and calibration data.
  • Prepare and check reagents and supplies. Perform calculations for work solutions or other calculations as required during experimental procedures.
  • Perform and document required routine maintenance and calibration of laboratory instruments.
  • Maintain the inventory of and order laboratory supplies including notifying instrument key operators of upcoming reagent/supply needs.
  • Process samples for analysis or storage.  Utilize PIMS/LIMS computer system for the processing of samples.
  • Assist the Laboratory Quality Coordinator with preparation for Internal audits and BELAC audits.
  • Identify new lab equipment if necessary
  • Support new lab technique (biomarkers, material, etc…)
  • Assisting in the validation of methods when it is necessary

Other

  • Provide ongoing and accurate information and support Volunteers/Patients regarding clinical trials to facilitate subject compliance
  • Monitor and document study subject compliance
  • Maintain accuracy, accessibility, and confidentiality in volunteer/patient records
  • Record and communicate or  resolve any discrepancy to study protocols in regards to laboratory
  • Facilitate positive attitude and trust by the volunteer/patient population toward participation in clinical research
  • Ensure development of new procedures required by the protocol as "superuser" and train staff accordingly
  • Perform safety inspection of laboratories and surrounding office area as assigned and prepare a report
  • May Participate in protocol reviews and provid specialized oversight and technical assistance in regards to the laboratory and liaise with the PI and the Clinical Project Manager
  • May be assigned to be mentor/sponsor for a new colleague

Training

  • Participate in training courses as appropriate
  • Organize and assist in the training of PCRU staff and contractors with less experience and expertise
  • May Ensure Lab training requirements are fully achieved  for protocol execution and for all protocol related procedures
  • Responsible for complying with Pfizer Standards, ethical standards, ICH, regulatory and legal requirements, national and European laws on health and safety at work, fire prevention and other appropriate legislation

Your Skills:

  • Minimum of a Diploma/Bachelor degree Medical Biology or equivalenty
  • Superior written and verbal skills are essential;including the ability to communicate complicated research priniciples in easily understandable language.
  • Must be available for various shifts (weekends/evenings/nights/public holiday)
  • English language skills is highly recommended, your second language would be French or Dutch
  • Excellent communication skills Minimum of 3 years of Laboratory experience

Clinical skills

  • Successful study conduct of all Clinical Research Unit studies in accordance with ethical, legal, and moral standards, Good Clinical Practices (GCPs) and Good Clinical Laboratory Practices (GCLPs), WRD management requests and drug development goals

Computer skills

  • Working knowledge of computers and ability to adapt rapidly and easily to clinical research data systems and associated issues/risks

Teamwork:

  • Demonstrates effective communication with management group and internal/external customers
  • Group members are able to perform and collaborate in teams to problem solve for increased team productivity
  • Must be proactive, showing initiative and positive team spirit
  • Accountability

Flexibility

  • Demonstrate ability and flexibility to work alternative or additional hours internally and externally (weekends/evenings/nights/public holiday) to provide study activity coverage

Language skills

  • Written and reading English skills is a must
  • Verbal French and dutch skills is an asset

Click here for notification and Apply

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