In Vivo Research Lead - CNS
Date: Apr 3, 2021
Location: Camden, NJ, US
Company: Spark Therapeutics
Join the Spark Team
We were born of innovation, springing from the curiosity, imagination and dedication of remarkable scientists and healthcare visionaries. Our shared mission is to challenge the inevitability of genetic disease by discovering, developing, and delivering treatments in ways unimaginable – until now.
We don’t follow footsteps. We create the path.
*Please Note: This position will have responsibilities at both the Rowan/Camden facility as well as the Pipersville location.**
The CNS In Vivo Lead will be responsible for scheduling, training and performing In Vivo studies in support of the CNS therapeutic areas and other therapeutic areas of the Non-Clinical department, if needed.
Additional responsibilities include but are not limited to:
- Oversee CNS In Vivo studies.
- Mentor and train In Vivo staff in CNS procedures.
- Schedule and follow multiple concurrent studies according to experimental design.
- Perform In Vivo studies, as needed.
- Review and ensure compliance with IACUC Protocols/amendments and EHS procedures.
- Oversee mouse breeding colonies.
- Perform ICV/Intrathecal/Intraparenchymal/IV/IP/PO/SC injections in mice and rats, monitor animal health, collect blood samples/CSF, and complete necropsies.
- Perform behavioral studies, brain surgeries as required.
- Ensure accurate data recording.
- Animal, general supplies, and reagent ordering.
- Interact with CNS team scientists and In Vivo Lead and provide constant feedback.
- Work cross-functionally with Liver and Ocular teams and provide support to other R&D In Vivo needs.
Responsibilities
% of Time |
Job Function and Description |
40% |
Oversee scheduling and execution of CNS procedures from team members. Assure IACUC compliance, proper procedure documentation and maintain accurate records of procedures. Communicate results/comments to study directors |
20% |
Perform and train team members in In Vivo techniques and animal monitoring according to applicable regulations in support of the CNS team and other therapeutic areas. |
20% |
Provide work assignments to the team on a regular basis. Review and approve the work performed by other team members. Ensure work is done in a compliant manner. |
20% |
|
Education and Experience Requirements
- Bachelor’s degree in relevant field required; Master’s degree, Ph.D. preferred.
- Generally has 5+ years of hands on relevant experience with rodents and managing people.
- Advanced skills on handling, restraining, dosing (IP, IM, and IV) and performing a variety of procedures on study animals required.
- Experience with managing transgenic mouse colonies required.
- Keep accurate records, follow instructions and comply with company policies.
- Ability to manage large mouse colonies required.
- Excellent organizational, communication and collaboration skills.
- Keep accurate records, follow instructions and comply with company policies.
- Experience with Gene Therapy is a plus.
- Previous experience in team leading is preferred.
- Experience with IACUC is a plus.
Key Skills, Abilities, and Competencies
- Strong organizational skills.
- Detail oriented
- Demonstrated ability to effectively manage multiple programs. Excellent record keeping.
- Excellent writing and verbal communication skills.
- Experience in training and supervising preferred.
- Experience in managing and working cross-functionally.
Complexity and Problem Solving
- Demonstrate independent problem-solving skills of technical issues.
- Develop solutions to a variety of moderate to complex problems; Discuss with supervisor and refer to policies/practices for guidance.
- Must be comfortable in the fast-paced, biotech start-up environment and interact with multi-disciplinary research teams at Spark.
- Exercise judgment within defined procedures and practices to determine appropriate action.
Internal and External Contacts
- CNS In Vivo Lead is accountable to the In Vivo Lead and serves as a key collaborator and peer to the In Vivo Therapeutic area Research teams.
- Will be in contact with Quality Assurance, Non-Clinical Operations, Clinical Operations, Pharm/Tox, Discovery, Assay Validation, R&D Operations, Technical Operations, Regulatory Affairs
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