Lab Technician / Lab Associate (CRO Project - IVD Industry)

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. 

Position Overview:

We are seeking a highly qualified Lab Technician/Lab Associate to join our team for a Contract Research Organization (CRO) project focused on clinical lab work and invitro diagnostic (IVD) development. The ideal candidate will have a background in clinical laboratories and at least 3 years of relevant experience in the IVD industry, whether in clinical trials or R&D. The role requires collaboration across disciplines, including regulatory, R&D, and clinical research. You will be involved in various aspects of the project lifecycle, from protocol development to reporting, and must be adaptable to changing duties as the project evolves.

Job Type: Full time  
Job Title: Lab Technician
Location: Onsite - San Diego

Salary Range: $20.00-$24.00

Key Responsibilities:

Perform laboratory procedures and experiments in accordance with clinical protocols.

Develop and review clinical study protocols under supervisor guidance.

Maintain accurate records of experiments and studies, documenting results and updates.

Prepare weekly reports and presentations (PowerPoint) on progress for management and team meetings.

Collaborate with R&D, regulatory, and clinical teams to ensure smooth project execution.

Communicate effectively with clients and cross-functional teams to prepare materials and testing kits for delivery.

Assist with the preparation and shipment of testing kits for clinical sites.

Follow Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).

Engage in regular communication with international colleagues, particularly those in China, and adapt to diverse cultural perspectives.

Requirements

• Bachelor’s degree in Biochemistry, Chemistry, or a related field is required.
• Minimum of 3 years in the IVD industry, either in clinical trials or related R&D roles.
• Strong background in clinical laboratory settings, with an understanding of regulatory requirements and protocols.
• Excellent communication skills, both written and verbal, with the ability to work well in a team.
• Experience with data recording and reporting, including proficiency in creating presentations and briefings for management.
• Ability to work in a multidisciplinary environment that includes regulatory, R&D, and clinical research functions. - Familiarity with the IVD product lifecycle and clinical trial processes.
• Key Competencies:
• Strong attention to detail and organizational skills.
• Adaptability and willingness to take on varied duties as required by project needs.
• Ability to work independently and follow procedures while collaborating with a larger global team.
• Problem-solving and critical-thinking skills in laboratory and clinical research environments.
• Ability to meet deadlines and work efficiently under pressure.

Benefits

Benefits

• Medical Insurance Plan
• Retirement Plan
• Paid Time Off
• Training & Development
  
  We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service