Lab Assistant

1. Always promotes the mission of the Knight Cardiovascular Institute through our Professional Standards of timely Customer Service, Reliability, Productivity, Professionalism, Accuracy, Timeliness, Integrity, and Problem-Solving.

2. Responsible for the lifecycle of bio samples while in the CTU from collection to shipping.
This includes but is not limited to:

• Works in collaboration with study coordinator to maintain and file regulatory and study documents of all samples collected for various studies.
• Keeps detailed accounting records of all samples processed, shipped, and stored.
• Creates and maintains a database of all bio samples in cryostorage.
• Processes samples after collection and prepares for shipping.
• Prepare, finalize, and deliver all packages for shipment at days end.
• Maintaining laboratory reporting and signature requests from the PI .

3. Benchtop research for investigator initiated clinical trials, including but not limited to:

• Perform various molecular techniques such as DNA/RNA/library preparation, PCR, Sanger sequencing, and other assays as deemed necessary.
• Gel preparation, loading, and imaging.
• Preparation of reagent solutions needed for molecular research.
• sample processing including DNA, RNA and protein.
• Monitor and maintain consistent laboratory day-to-day operations, assist with purchases of equipment and supplies, and oversee maintenance of equipment.

4. General Laboratory:

• Perform general lab upkeep and record keeping as necessary.
• Provide support to stocking laboratory.
• Provide support in laboratory cleaning and decontamination.
• Provide support and training to new clinical trials staff who are familiarizing themselves with sample processing.

5. Data Collection/Data Analysis/Record Keeping:

• Collect scientific data pertinent to research projects, keep records of information (which may include database searches).
• Maintain integrity of all databases, including sponsor EDC as required.

6. Report Preparation and Literature Research:

• Prepare reports containing analytical, descriptive, and evaluative content that will be submitted for publication, grant applications, progress reports, presentations at national and international meetings, etc.
• Assist the Clinical Trial Managers, coordinators, or Principle Investigator with other research related projects and administrative/office related duties as needed.
• Assist manager and coordinator as needed in supporting sponsor visits (i.e. proctoring visits, monitoring, site initiation, etc.)

• Education: Bachelor's in relevant field OR

• Associate's AND 3 years of relevant experience OR

• 4 years of relevant experience

• Previous work with scientists in an academic environment
• Ability to prioritize multiple tasks at one time
• Must have working knowledge of basic lab functions and general benchtop skills.
• Must have excellent communication, analytical and organizational skills: both written and verbal.
• Ability to work independently and as part of a team while being collaborative in resolving problems.
• Must be proficient with computers running Windows and PC applications e.g. MS Excel, Oracle, Access, Word and PowerPoint).
• Must have demonstrated excellent customer service skills both on the phone and in person.
• Demonstrated ability to work with a variety of diverse individuals and personalities.
• Must possess energy and drive to coordinate multiple projects simultaneously.
• Ability to use tact and diplomacy to maintain effective working relationships.

• Bachelor's degree with coursework in Science

• 3 years of relevant research experience, with demonstrated research or clinical experience in molecular biology and knowledge of cardiology.

• Managing Access database or similar database.

• Microsoft office, medical terminology, analytical skills, trouble shooting skills, and independent laboratory skills.
• Ability to work independently as well as within a team environment.
• BLS