JUMP TO CONTENT

Medical Technologist II - Monday-Friday 8a-5p

JR063692

About the role

This vacancy has now expired. Please see similar roles below...

Each individual performing high complexity testing must

1) Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results;

2) Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;

3) Adhere to the laboratory's quality control policies,

4) Document all quality control activities, including instrument and procedural calibrations and maintenance performed;

5) Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance;

6) Be capable of identifying problems that may adversely affect test performance or reporting of test results;

7) Demonstrate knowledge and capacity to either correct the recognized problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director;

8) Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications

Required Experience

Applicant should have at least 4 years of experience in a Clinical Molecular Laboratory that includes:

  • Nucleic acid extraction from blood, bone marrow aspirate, FFPE tissue, plasma
  • Utilization of Next Generation Sequencing (NGS) and PCR-based clinical assay methods and platforms

Applicant should have strong knowledge, skill, and/or abilities in:

  • Good documentation practices
  • College of American Pathologist (CAP) requirements and guidelines
  • Excellent written, verbal, and interpersonal communication skills
  • Proficient use of computers/scanners/copiers/printers, including Word and Excel applications
  • Demonstrated knowledge of operational characteristics of apparatus, equipment, and materials used in a regulated clinical laboratory
  • Sterilization and decontamination techniques, including hazardous waste disposal
  • Commitment to participate as a constructive, contributing team member of a dynamic, clinical diagnostic work group
  • Commitment to compliance with all MolecularMD/ICON safety and regulatory work practice guidelines and procedures as defined in the Quality Management Program, the Chemical Hygiene Plan, confidentiality and HIPAA agreements, and all applicable state and federal regulations and requirements

Education and Work Experience

  • BA/BS in Biology, Molecular Biology, Medical Technology or Molecular Biology, or related science and 4 years of experience in a Clinical Molecular Laboratory
  • or Master's Degree in Biology, Molecular Biology, or related science and 2 years of experience in a Clinical Molecular Laboratory
List #1

Day in the life

Endometriosis yellow ribbon
Shining a Light on Endometriosis Awareness Month

Teaser label

Inside ICON

Content type

Blogs

Publish date

04/18/2024

Summary

Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis

Teaser label

Endometriosis Awareness Month sheds light on this often-misunderstood condition affecting millions worldwide.

Read more
Data visualisation
The Role of Data Management in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

04/18/2024

Summary

Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

Teaser label

This blog examines the critical role of data management in clinical trials.

Read more
Medicine on a shelf
Navigating the Clinical Research Supply Chain

Teaser label

Industry

Content type

Blogs

Publish date

04/12/2024

Summary

Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ

Teaser label

Discover the intricate workings of the clinical research supply chain in this comprehensive guide.

Read more
View all

Who we are

Press play to find out more

Similar jobs at ICON

Clinical Trial Assistant 1

Salary

Location

Warsaw

Department

Clinical Operations Roles

Location

Warsaw

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109680

Expiry date

01/01/0001

Read more Shortlist Save this role
Graduate Pharmacovigilance Associate

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109722

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Project Analyst I

Salary

Location

Mexico, Mexico City

Department

Full Service - Development & Commercialisation Solutions

Location

Sao Paulo

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Project/ Program Management

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

JR118270

Expiry date

01/01/0001

Ana Lucia

Author

Ana Lucia
Ana Lucia

Author

Ana Lucia
Read more Shortlist Save this role
Laboratory Proj Coordinator I

Salary

Location

Mexico, Mexico City

Department

Full Service - Development & Commercialisation Solutions

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Project Management

Job Type

Permanent

Description

JR118149Laboratory Proj. CoordinatorSite: Mexico, Mexico CityOffice BasedAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us

Reference

JR118149

Expiry date

01/01/0001

Fernanda Bezerra Read more Shortlist Save this role
Senior Clinical Trial Associate - Hybrid Office-Based in Waltham, MA

Salary

Location

Boston

Department

Clinical Operations Roles

Location

Boston

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109962

Expiry date

01/01/0001

Read more Shortlist Save this role
Senior CRA

Salary

Location

Poland

Department

Clinical Monitoring

Location

Poland

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109995

Expiry date

01/01/0001

Michal Czyrek

Author

Michal Czyrek
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above