Biospecimen Coordinator

Responsibilities

• Receive, sort, and perform accurate data entry for all specimens entering the laboratory.
• Verify information on requisition forms with collection containers for accuracy.
• Capture and enter specimen information into computer database systems such as LIMS and Bioinventory.
• Document within the electronic master file, including uploading/completing documents and using document exchange portals.
• Keep up with multiple project protocols and requirements.
• Examine specimens for adequacy and label and measure volumes for samples.
• Meet key production metrics and quality measures to ensure timely and accurate sample processing.
• Take pictures of data on specimen containers for quality control.
• Pack and ship specimens to appropriate facilities when required.
• Properly store specimen samples as needed.
• Aid clients and project managers with inquiries about specimen requirements and test turnaround times.
• Identify and document situations that may impact sample integrity, notifying management and project managers.
• Handle and dispose of medical and chemical waste responsibly.
• Sort and prepare paperwork for scanning.
• Answer the loading dock door for incoming shipments and couriers.
• Perform administrative duties including filing paperwork and answering phones.
• Sanitize work stations regularly.
• Work collaboratively with all team members and demonstrate respect for all colleagues.
• Comply with applicable laws, regulations, and company procedures and policies.

Essential Skills

• Bachelor's Degree in the Sciences (Biology Preferred)
• Strong data entry skills with proficiency in typing
• Previous experience in a clinical laboratory or related work environment
• Proficient with MS Office and Teams
• Outstanding communication skills, both written and verbal
• Outstanding organizational skills
• Ability to handle biological materials and perform high-level accuracy tasks
• Comfortable handling human biological specimens including blood, urine, and tissue samples
• Ability to lift up to 40lbs, work in protective equipment, and sit/stand for long periods
• Ability to work both independently and in a team environment
• High level of attention to detail with problem-solving skills
• Ability to work overtime when needed

Additional Skills & Qualifications

• Clinical Trial Experience is preferred
• Previous medical/laboratory experience is a plus
• Medical tech background or medical assistant experience is advantageous
• Science background or knowledge is beneficial
• Experience with specimen collection, processing, handling, and labeling is valuable

Work Environment

You will be working in a biobanking, bioprocessing, and analytics environment, with a focus on handling incoming samples such as saliva, DNA, blood, stool, and urine. This role requires the ability to lift up to 40lbs, work in protective equipment, and sit/stand for long periods. You will be contributing to important health initiatives, making a significant impact during the health crisis.

Job Type & Location

This is a Contract position based out of Piscataway, NJ.

Pay And Benefits

The pay range for this position is $22.00 - $22.00/hr.

Requirements

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.