Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases. Our next-generation genome-editing technology enables superior precision to develop cell therapies that are armored to potentially improve activity against diseases. We believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases.
Members of the Caribou herd open their minds to new ideas and welcome diverse perspectives. We proudly assert that teams do their best work when their members are personally engaged, their ideas are taken seriously, and contributions are recognized. Members of the herd work from our headquarters in Berkeley, California, or remotely.
Our fun and collaborative Clinical Development team is seeking an innovative and highly motivated Clinical Research Scientist with a background in hematology-oncology and cell therapy to support our clinical development strategy and plans. Reporting to the Associate Director of Clinical Research, you will be responsible for delivery on clinical study designs, high quality trial execution, and preparation of clinical protocols.
Responsibilities:
- Manage clinical studies including planning, execution, completion, and reporting
- Review and analyze clinical data and assist in generating study reports, publications, and regulatory documents
- Conduct data review, analysis, and interpretation of clinical trials data
- Follow safety and data review plans to perform and document regular review of patient safety data and perform review of cumulative safety data
- Draft clinical and safety sections of critical documents
- Support and assist in the development of publications, abstracts, and presentations
- Partner with cross-functional functions (i.e. translational science, data management and clinical operations) as needed to ensure compliance with GCP and quality execution of plans that involve patient samples and analysis
- Develop and maintain professional relationships with internal and external stakeholders
Qualifications:
- PhD/PharmD and 5+ years of experience in clinical development; MA/MS/MSN and 8+ years of experience; BA/BS/BSN and 10+ years of experience
- Experience in hematology-oncology drug development (preferably acute myeloid leukemia)
- Proven scientific writing skills and good communication skills
- Experience with GCP
- Experience with data listing review
- Ability to perform data analysis
Additional Requirements:
- Availability during normal business hours in the employees’ time zone (hybrid or remote position)
- Availability to travel to clinical study centers and to Caribou Biosciences meetings in California as needed
- Must live in a pre-registered state to be eligible for remote role at Caribou Biosciences (CA, WA, AZ, FL, GA, IL, MA, MN, NJ, NC, TX, VA, NY, CO, OR)
Nice-to-haves:
- Experience in a start-up environment
- Experience with product launch activities
- Background in hematology-oncology
Caribou compensation and benefits include:
- Comprehensive compensation package, which includes competitive salary, bonus, and equity for all employees
- Salary Range: $135,000 to $155,000 – This represents the present low and high end of the Company’s pay range for this position. Actual pay will vary based on various factors, including but not limited to location, skill, experience, and performance.
- Generous paid vacation time, in addition to company-observed holidays and floating holidays
- Excellent medical, dental, and vision insurance
- 401(k) retirement savings plan, which includes matching employer contributions
- Employee stock purchase plan (ESPP)
- Tuition reimbursement program
The benefits and stock purchase described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility.
Caribou is an equal opportunity employer and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, or any other basis protected by law. In addition, Caribou prohibits the harassment of any individual on any of the bases listed above or any other characteristics protected under federal, state, or local laws.
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
We do not accept unsolicited resumes or candidate submissions from staffing agencies. All agencies must have a valid written agreement with Caribou Biosciences, Inc.for service in place. Any resume or candidate submitted by a staffing agency without such an agreement in place will be considered unsolicited, and Caribou Biosciences, Inc. will not be obligated to pay any referral or placement fee.