Research Associate, Protein Engineering

Atreca Redwood City , CA 94063

Posted 4 months ago

Who We Are:

Atreca is a dynamic biotechnology company located in Redwood City, California. We apply our Immune Repertoire Capture (IRC) technology to profile the clinically relevant, active B cell responses of patients and build a portfolio of tumor-targeted antibodies. These patient-derived antibodies fuel our discovery of novel targets and development of cancer immunotherapeutics.

Job Description:

We are seeking an outstanding, enthusiastic, and highly motivated Research Associate to join our Protein Engineering group. The successful candidate will become a key member of the research team, supporting production and characterization of antibodies identified from our IRC platform, as well as engineered bispecifics and other antibody-based formats.

Responsibilities:

  • Produce and characterize antibodies and bispecifics

  • Catalog and integrate materials and results into informatics systems

  • Enable faster and higher-throughput cycles of design/build/test/learn

  • Follow laboratory safety guidelines and practices

  • Work with other project team members and communicate results with the team

Requirements:

  • BS/BA or MS in bioengineering, chemical engineering, molecular biology, biochemistry, immunology, or related discipline with lab experience required

  • 0-5 years of relevant career experience

  • Experience with recombinant protein production required (high-throughput preferred)

  • Experience with FPLC, HPLC, SDS-PAGE preferred

  • Experience with HEK293 or CHO cell culture preferred

  • Experience with DNA technologies preferred (cloning, bacterial culture, plasmid preps, and sequence verification)

  • Experience with bispecific antibodies a plus

  • Strong analytical skills, excellent communication skills, and attention to detail

  • Track record of being adaptable, self-motivated, and scientifically rigorous

  • Ability to work in a team, prioritize tasks, and drive projects to completion

Exact title commensurate with experience. Atreca is an equal opportunity employer.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Clinical Research Coordinator Associate

Stanford University

Posted 2 days ago

VIEW JOBS 10/15/2019 12:00:00 AM 2020-01-13T00:00 Stanford University Department of Dermatology is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies. The CRCA will coordinate moderately complex aspects of one or more clinical studies and work under close direction of the principal investigator and/or study coordinator/supervisor. The CRCA will support federal and non-federal clinical research studies including dermatological and investigative work in support of clinical trials, clinical research or biomedical research focusing on "bench to bedside" treatment. Duties include: * Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. * Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. * Coordinate collection of study specimens and processing. * Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. * Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. * Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. * Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff. * Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. * Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements. * Participate in monitor visits and regulatory audits. * - Other duties may also be assigned DESIRED QUALIFICATIONS: * A Bachelor degree with an educational background in medicine and/or scientific field (biological sciences, social sciences, etc.) * Strong oral and written communication skills * Excellent attention to detail * Able to problem solve * Team player * Positive attitude * Adapts to change well * Proficiency in using computers, software, and web-based applications in a previous administrative setting EDUCATION & EXPERIENCE (REQUIRED): Two year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): * Strong interpersonal skills. * Proficiency with Microsoft Office. * Knowledge of medical terminology. CERTIFICATIONS & LICENSES: Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. PHYSICAL REQUIREMENTS*: * Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. * Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds. * Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. * - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. WORKING CONDITIONS: Occasional evening and weekend hours. Based in Redwood City, Discovery Hall, Stanford University WORK STANDARDS: * Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. * Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned. * Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu. Additional Information * Schedule: Full-time * Job Code: 4924 * Employee Status: Regular * Grade: F * Department URL: http://dermatology.stanford.edu * Requisition ID: 83368 Stanford University Redwood City CA

Research Associate, Protein Engineering

Atreca