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Precision Biosciences Jobs (NOW HIRING)

$69 - $101/hr

Rancho BioSciences is a globally recognized leader in providing advanced services and products ... precision medicine . Our mission is to bridge science and healthcare, helping to transform data ...

VP, CMC

Waltham, MA · On-site

$300 - $340/hr

VP, CMC Korsana Biosciences, Inc. Waltham, Massachusetts, United States About this positionAbout Us ... Our mission is to advance precision-engineered therapies, designed to address some of the biggest ...

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Precision Biosciences information

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How much do precision biosciences jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for precision biosciences in the United States is $16.59, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $16.83 per hour, depending on experience, location, and employer.

What is Precision Biosciences?

Precision Biosciences is a biotechnology company that specializes in developing genome editing technologies, with a focus on creating gene therapies for serious genetic diseases and cancer. Their proprietary ARCUS® genome editing platform allows for precise DNA editing, which can be used to develop innovative treatments. The company is involved in both in vivo gene editing programs and allogeneic cell therapies, aiming to address unmet medical needs and improve patient outcomes.

What are the key skills and qualifications needed to thrive as a Precision Biosciences scientist?

To thrive as a scientist at Precision Biosciences, you typically need a strong background in molecular biology, gene editing, and cellular biology, supported by an advanced degree in a relevant scientific field. Experience with gene editing platforms like ARCUS, CRISPR, next-generation sequencing, and data analysis software is highly valued. Key soft skills include problem-solving, attention to detail, and effective teamwork and communication. These competencies are crucial for advancing innovative therapies, maintaining research accuracy, and collaborating efficiently in a fast-evolving biotechnology environment.

What are some common challenges faced by employees working at Precision Biosciences, and how does the company support professional growth?

Employees at Precision Biosciences often work at the forefront of gene editing technology, which can involve fast-paced projects and the need to adapt quickly to new scientific developments. Balancing innovation with regulatory compliance is a key challenge, as is collaborating across multidisciplinary teams. To support professional growth, Precision Biosciences offers opportunities for ongoing learning, mentorship, and clear pathways for advancement within both scientific and operational tracks. The company fosters a collaborative environment that encourages cross-functional teamwork and knowledge sharing.

What is the difference between Precision Biosciences vs CRISPR Research Scientist?

AspectPrecision BiosciencesCRISPR Research Scientist
Primary RoleDevelops gene editing therapies using proprietary platformsConducts research and experiments using CRISPR technology
Work EnvironmentBiotech companies, laboratories, research institutionsAcademic labs, biotech firms, research institutions
Required CredentialsAdvanced degrees in molecular biology, genetics, or related fieldsMaster's or PhD in biology, genetics, or related disciplines
Industry UsageBiotech, pharmaceutical, gene therapy companiesResearch institutions, biotech startups, pharma companies

While both roles involve gene editing technologies, Precision Biosciences focuses on developing proprietary platforms for therapeutic applications, whereas CRISPR Research Scientists primarily conduct experiments and research using CRISPR tools. The roles often overlap in credentials and work environments, but their objectives differ—one is product development, the other research-focused.

More about Precision Biosciences jobs

What states have the most Precision Biosciences jobs?

States with the most job openings for Precision Biosciences jobs include:

Infographic showing various Precision Biosciences job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, 12% Part Time, 3% Contract, and 2% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $34,500 per year, or $16.6 per hour.

Sr. Director/Vice President of Clinical Development

Merida Biosciences

Cambridge, MA • On-site

Full-time

Re-posted 17 days ago


Job description

Description:Sr. Director/Vice President of Clinical Development


At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and completely eliminate the root causes of autoimmune and allergic diseases, and to achieve deep, durable responses while preserving essential immunity. We are looking for passionate individuals to join our mission to transform treatment paradigms across the spectrum of antibody-driven diseases.  


Merida Biosciences is seeking an experienced and strategic Sr. Director/Vice President of Clinical Development to lead the clinical strategy and execution across two innovative development programs. This individual will play a critical leadership role in shaping and advancing early- and mid-stage clinical development plans, driving cross-functional collaboration, and serving as a key contributor to the overall development strategy of the company.


The ideal candidate will bring deep expertise in allergy, immunology, autoimmune, and antibody-mediated diseases, along with a strong track record of advancing novel therapeutics through clinical development. This role requires both strategic vision and operational excellence in a fast-paced biotechnology environment.


Key Responsibilities

· Lead clinical development strategy and execution for two Merida Biosciences therapeutic programs from IND through proof-of-concept and beyond

· Serve as the clinical leader and subject matter expert in allergy and antibody-driven diseases, helping shape indication strategy and development priorities

· Serve as clinical development lead for 2 cross-functional Program Teams focused on providing strategic input into target product profiles, indication prioritization, competitive positioning, and lifecycle planning across allergic and autoimmune indications; facilitate alignment of Program Strategy across the clinical organization

· Responsible for clinical development deliverables for each Program, including design and oversight of clinical development plans, protocols, study endpoints, and clinical trial execution in collaboration with Clinical Operations, Regulatory, Translational Sciences, Biometrics, and Medical Affairs

· Serve as the medical and scientific lead for assigned programs internally and externally, including interactions with investigators, advisors, partners, and regulatory agencies

· Collaborate closely with translational and research teams to integrate biomarker and mechanistic insights into clinical strategy

· Contribute to regulatory submissions and represent Clinical Development in interactions with FDA and global health authorities

· Build and maintain relationships with key opinion leaders, clinical investigators, and patient advocacy organizations within the allergy and immunology communities

· Partner cross-functionally to ensure alignment on timelines, budgets, and development milestones

· Support data interpretation, safety reviews, and presentation of clinical findings to leadership, boards, and external stakeholders

· Mentor and help build a high-performing clinical development organization as the company grows

Requirements:


· MD, MD/PhD, or equivalent advanced medical/scientific degree required

· 12+ years of biotechnology or pharmaceutical industry experience, including significant clinical development leadership experience

· Deep expertise in allergy and immunology required, including experience in allergic diseases, antibody-mediated disorders, or related inflammatory conditions

· Demonstrated success advancing clinical-stage therapeutics through Phase 1 and Phase 2 development

· Experience with biologics, antibody therapeutics, Fc-engineering platforms, or precision medicine approaches highly desirable

· Strong understanding of clinical trial design and endpoints in allergy and immunology indications

· Deep understanding of regulatory strategy, safety assessment, and translational medicine

· Proven ability to lead cross-functional teams and influence across organizations

· Strong communication and presentation skills with experience interacting with executive leadership and external stakeholders

· Entrepreneurial mindset with the ability to thrive in a dynamic, fast-moving biotech environment


Compensation: We understand that compensation is an important part of considering a new opportunity. Our goal is to be transparent so there are no surprises at the end of the process, and you can feel confident that your offer is both fair and equitable. To support that, we’re sharing our hiring range for this role upfront: typically for the Senior Director level we target $245,000 to $300,000. The final offer will take into account a number of factors, including your skills, experience, location, market data, and internal equity. Along with a competitive salary, we’re proud to offer a comprehensive benefits package designed to support you both personally and professionally.


Merida Biosciences is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.