Lab Technologist

Stago Group; Mount Olive (NJ); On-site; USD 70,000 - 85,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k

PTO

Life insurance

Disability insurance

Comprehensive leave program

Job summary

Stago Group in Mount Olive, NJ is seeking a skilled professional to oversee clinical trials and support product launches in Hematology and Hemostasis. This role demands a solid background in hematology and experience with instrument validation, ensuring study protocols are effectively executed.

The position offers a comprehensive benefits package including medical, dental, and 401k, with salaries ranging from $70,000 to $85,000 based on qualifications.

Qualifications

• Minimum five years experience in Hematology and Coagulation.
• Experience with instrument validations and training lab staff.

Responsibilities

• Provide input to clinical trial designs and execution.
• Verify technical conditions prior to the start of a study.
• Manage Laboratory equipment service contracts.

Skills

Instrument validation

Hematology knowledge

Coagulation experience

Clinical trial regulations

Education

B.S. in Medical Technology/Clinical Laboratory Science

MT(ASCP) Certification

Job description

DSI Warehouse/Office
330 Waterloo Valley Road
Mount Olive, NJ 07828, USA

• Stays current with instrument capabilities and clinical trial regulations in order to provide input to clinical trial designs and execution.
• Interacts with groups, such as, but not limited to CLSI, CLIA and CAP in order to ensure Stago is at the forefront of the market's evolution.
• Works closely with French counterparts to help conduct and support R&D activities as well as clinical trials in the US in facilitation of new Hematology and Hemostasis product launches.
• Participates in the development of study protocols and ensures study designs are appropriate for execution in the lab.
• Verify technical conditions prior to the start of a study, ensure instruments are in pristine working order and maintenance of equipment is up to date to ensure successful study conditions.
• Utilizing local members of the service operations, create good logistical conditions for clinical studies to include but are not limited to delivery of reagents and/or instrument, specimens, exchange of correspondence, contracts and administrative documents.
• Ensures full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizational time lines.
• Works closely with the NCRA for all necessary study follow-up in accordance with defined procedure including but not limited to the checklist for site initiation and monitoring visits, etc.
• Ensure corrective actions are followed for proper conduct to freeze databases of results in accordance with the studies initial objectives.
• Check completeness of records (all forms of media: paper and electronic), ensures centralization and formatting of data from studies, as well as ensuring traceability of data.
• Uses knowledge and experience with instrument validation, interference, on-board stability, Limit of Blank, Limit of Detection, Limit of quantification to perform Linearity and Method Comparison testing.
• Maintain laboratory equipment following daily, weekly and monthly maintenance schedules as well as required quality control for all laboratory analyzers.
• Participates in validation of new equipment as appropriate.
• Assists the NCRA’s in the development and maintenance of clinical study binders and utilization of eCRF.
• Manages the Laboratory equipment service contracts and documentary elements of clinical trial activities;
• Completes necessary clinical trial documentation from the site's perspective, in preparation of study start up.
• Give scientific presentations as required.
• Offer support on new product launches as needed.

Education and/or Experience:

• B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required.
• MT(ASCP) Certification or equivalent preferred.
• Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation.

Travel may be required for this position up to 10%, must be able to travel internationally.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

We offer an extensive benefit and compensation package that includes medical, dental, vision, FSA, 401k, PTO, life and disability insurance, as well as a comprehensive leave program. Pay anticipated for this position in New Jersey is from $70,000-$85,000, depending on a number of factors. This role is also anticipated to be eligible to participate in a bonus plan and an automobile plan which are associated with this position. In the ordinary course of business, compensation and benefits programs may change based upon the Company’s needs.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.