CrawlJobs Logo

mRNA Science Intern

beamtx.com Logo

Beam Therapeutics

Location Icon

Location:
United States , Cambridge

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

23.00 - 34.00 USD / Hour

Job Description:

Beam is looking for a highly energetic and motivated summer intern to join our mRNA Science team from June to August of 2026. The intern will assist in producing and screening mRNA—which codes for the base editor protein—with novel sequence designs and chemical modification to enhance the potency and specificity of the mRNA used across multiple programs. Specifically, this role will involve performing and optimizing in vitro transcription (IVT) reactions and running biochemical assays and chromatographic analysis to characterize the mRNA products. The ideal candidate for this role is detail-oriented, persistent, highly organized, and has an innovative mindset toward solving technical challenges. This position will play a central role in advancing our core mRNA technology, while providing individual exposure to one of the most important classes of medication of the 21st century.

Job Responsibility:

  • Produce mRNA with novel sequences and chemistry via IVT reactions
  • Thoroughly analyze the product by capillary electrophoresis, gel electrophoresis, and high-performance liquid-chromatography
  • Work collaboratively with other teams to perform editing experiments in cells
  • Maintain detailed documentation of experiments in the ELN system
  • Adhere to all laboratory safety requirements and procedures

Requirements:

  • Pursuing a BS or MS in biological sciences or a related field (Bioengineering, Biochemistry/Biophysics, Cell Biology/Molecular Biology) with at least 1 year of relevant laboratory experience
  • Knowledge of biochemical & molecular biology methods used in drug discovery and development
  • Proficiency in Excel, PowerPoint, and data analysis
  • Experience maintaining a lab notebook and following written protocols
  • Motivated to learn and detail oriented with excellent organizational and communication skills
  • Currently enrolled in a degree-granting college or university program and maintain student status throughout the internship

Additional Information:

Job Posted:
January 06, 2026

Work Type:
Hybrid work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for mRNA Science Intern

New

Associate Director, Quality Control Technical Services

Beam Therapeutics is a biotechnology company committed to establishing the leadi...
Location
Location
United States , Cambridge
Salary
Salary:
185000.00 - 225000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree (MS, Ph.D) in Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline, with 8+ years of relevant industry experience in Quality Control, Analytical Development, or CMC within biologics, cell therapy, or gene therapy
  • Extensive hands-on experience with ex vivo autologous cell therapies, including CD34+ cell-based products, across late-stage development, validation, and/or commercial readiness
  • Demonstrated technical expertise in cell handling and testing methodologies, including functional and potency assays, flow cytometry, NGS-based assays, and separation sciences. Experience with analytical method automation, qualification, and validation is strongly preferred
  • Proven understanding of analytical method lifecycle management, including method transfer, qualification, validation, performance monitoring, remediation, and comparability, particularly for late-stage and commercial products
  • Strong working knowledge of US and EU regulatory expectations (e.g., FDA/CBER, EMA, ICH, USP) applicable to cell and gene therapy CMC, with the ability to apply guidance in a phase-appropriate and inspection-ready manner
  • Direct experience supporting regulatory submissions (INDs, BLAs, amendments, post-approval changes) for cell and gene therapy products, including specifications, method validation reports, and responses to health authority questions
  • Demonstrated ability to lead and influence cross-functional program teams, partnering effectively with CMC, Manufacturing, Analytical R&D, Quality Assurance, and Regulatory Affairs in a fast-paced, matrixed environment
  • Strong communication and leadership skills, with a track record of clearly articulating technical strategies, aligning stakeholders, and driving decisions across functions and with external partners
  • Documented success in driving complex, program-critical initiatives to completion on time and within budget, including managing dependencies, risks, and priorities across multiple workstreams
  • Highly developed organizational, analytical, and problem-solving skills, with the ability to interpret complex datasets, assess risk, and translate data into actionable QC and CMC strategies
Job Responsibility
Job Responsibility
  • Lead and influence QC CMC strategy in partnership with cross-functional CMC teams for master cell banks (MCBs), plasmids, and mRNA drug substance and critical materials, supporting both ex vivo and in vivo therapy programs across development and commercialization
  • Define and execute the QC testing, method strategy, and technical execution to enable next-generation autologous cell therapy manufacturing processes, including analytical readiness for process validation, comparability, and technology transfer
  • Own and coordinate analytical method transfer, qualification, and validation activities across internal and external QC laboratories, ensuring compliant, phase-appropriate, and inspection-ready execution
  • Establish and maintain analytical control strategies by tracking and trending in-process, release, and stability data, collaborating with statisticians and program teams to define and justify specifications for MCBs, plasmids, mRNA, and autologous cell therapy products
  • Define and oversee stability strategies and programs for MCBs, plasmids, mRNA, and ex vivo cell therapy products, ensuring alignment with regulatory expectations and lifecycle needs
  • Lead analytical method lifecycle management for late-stage and commercial ex vivo portfolio, including method performance monitoring, remediation, comparability activities, and continuous improvement
  • Drive the internalization of validated mRNA analytical methods into Beam's North Carolina Quality Control laboratory, strengthening internal capabilities and supporting long-term commercial supply
  • Author and review Quality System documentation, including SOPs, Change Controls, and CAPAs, to support method implementation, lifecycle changes, and inspection readiness
  • Partner with Regulatory Affairs-CMC to author, review, and coordinate CMC sections of regulatory submissions, including specifications, method validation reports, and responses to agency queries
  • Ensure QC visibility and alignment on regulatory interactions, including tracking agency questions, commitments, post-approval requirements, and method introduction or change strategies
  • Fulltime
Read More
Arrow Right

Analyst, Quality Control, Chemistry & Stability

The Role: Joining Moderna offers the unique opportunity to be part of a pioneeri...
Location
Location
Australia , Melbourne
Salary
Salary:
Not provided
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BSc in a relevant scientific discipline (Chemistry preferred) with 5 years Quality Control experience in a cGMP organization with a focus in Analytical Chemistry
  • Hands on experience with analytical chemistry techniques including, but not limited to, HPLC, UPLC, particle analysis and plate reader-based assays
  • Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred
  • Working experience in a GMP environment
  • Ability to collaborate effectively in a dynamic, cross-functional matrix environment
  • Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment
  • Proven ability to conduct investigations
Job Responsibility
Job Responsibility
  • Perform GMP QC Chemistry methods including HPLC, UPLC, UV, and Particle Analysis via Dynamic Light Scattering
  • Execute HPLC (AEX) and NaOH plate reader-based assays to support process stat testing
  • Support method transfer projects internally and externally in collaboration with Analytical Sciences & Technology (AS&T) teams
  • Execute general lab operational tasks aligned with cGMP, including reagent preparation, equipment maintenance, and good documentation practices
  • Provide audit support for both internal and regulatory inspections
  • Create, review, and revise SOPs, protocols, and reports aligned with evolving quality standards and compliance frameworks
  • Support all stability program operations: perform sample set downs, pulls, inventory checks, labeling, and data entry in LIMS and inventory systems
  • Maintain and trend stability data using statistical analysis
  • produce stability tables, charts, protocols, and final reports
  • Troubleshoot assay methods and lab equipment as needed
What we offer
What we offer
  • Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right

2026 Co-Op, Drug Product Development

Location
Location
United States , Norwood
Salary
Salary:
20.00 USD / Hour
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Current student enrolled in a Bachelor’s or Master’s program in Chemical Engineering, Biochemical Engineering, Bioengineering, Biomolecular Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics, Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related field
  • Strong fundamental scientific and engineering skills for the evaluation of experimental data
  • Laboratory skills applicable to bioprocess development and analytical methods
  • Candidates must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship.
Job Responsibility
Job Responsibility
  • Work with a team of highly skilled experts to come up to speed on technology and techniques
  • Use laboratory, technical and communication skills to generate experimental results, perform data analysis, and document in formal reports including conclusions and recommended next steps
  • Perform process scale-up, support technology transfer, and provide manufacturing support at internal Moderna, and external contract manufacturing sites
  • Participate in planning, design, execution, analysis of experiments and formal risk assessments to establish critical process parameters, and overall process control strategies
  • Optimize the impact of formulation and processing conditions on the stability of mRNA drug products and process intermediates
  • Review and share relevant academic literature and establish new collaborations with internal research and manufacturing groups
  • Create scaled-down models, and high-throughput experimental setups for unit operations
  • Characterize mRNA and lipid nanoparticles through collaboration with the analytical team
  • Design and execute stability studies, including in-use, hold-time, and compatibility studies, to assess drug product robustness under clinically relevant conditions
  • Prepare technical reports and present findings in cross-functional meetings.
What we offer
What we offer
  • Free premium access to meditation and mindfulness classes
  • Subsidized commuter benefits
  • Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown
  • Location-specific perks and extras
  • Eligible for an annual discretionary bonus, other incentive compensation, or equity award.
  • Fulltime
Read More
Arrow Right

National Market Access Lead

Joining Moderna offers the unique opportunity to be part of a pioneering team th...
Location
Location
Germany , Munich
Salary
Salary:
Not provided
modernatx.com Logo
Moderna
Expiration Date
June 08, 2026
Flip Icon
Requirements
Requirements
  • University degree in science, economics, public health or related field
  • advanced degree (MBA, PhD) preferred.
  • 8+ years of experience in pharmaceutical market access, pricing, HEOR, public health or related roles, ideally with exposure to vaccines.
  • Deep expertise in German access pathways and reimbursement systems, including proven experience engaging with national HTA and public health stakeholders.
  • Demonstrated leadership experience in shaping or driving national market access strategies.
  • Strong analytical capabilities with hands-on expertise in real-world evidence and claims data analysis.
  • Proven expertise in German vaccine access pathways and national reimbursement environments.
  • Hands-on experience with pricing strategy development and innovative access models.
  • Track record supporting or leading dossier development (AMNOG (§35a SGB V)).
  • Demonstrated success in cross-functional leadership and stakeholder management at senior levels.
Job Responsibility
Job Responsibility
  • Lead the development and execution of national market access strategies across vaccines and pipeline therapeutics.
  • Own pricing and contracting approaches aligned with global and regional frameworks, tailored to German policy.
  • Shape national HTA and reimbursement positioning, including readiness for evolving policy requirements.
  • Oversee national dossier development and submission processes (e.g., AMNOG/§35a SGB V), ensuring robust, evidence-based access narratives.
  • Serve as Moderna’s lead representative to key national health institutions and payers, including G-BA, RKI, GKV-SV, and STIKO (in support of the medical team).
  • Drive claims and RWE (real-world evidence) analyses to inform pricing, reimbursement, and contracting strategies.
  • Define local evidence needs in partnership with global and local HEOR, including burden-of-disease, epidemiology, and payer-relevant data.
  • Translate scientific and real-world datasets into compelling payer value stories and clear evidence frameworks.
  • Coordinate cross-functional teams (Market Access, HEOR, Medical, Commercial, external experts) for strategy execution.
  • Act as an internal consultant to align local market insights with global product and platform plans.
What we offer
What we offer
  • Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right

Manager, Regional Regulatory Strategist

As a Manager, Regional Regulatory Strategist, you will play a critical role in a...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in Life Science or related discipline, advanced degree preferred (PharmD, MSc, PhD)
  • 5+ years of experience in the pharmaceutical industry. 3+ years of experience in Regulatory strategy
  • Strong experience with CTD format and content of regulatory filings
  • Knowledge of and broad experience with regulatory procedures and legislation for drug development, product registration, line extension and license maintenance in the EU and/or relevant International markets
  • Ability to work independently to manage multiple projects in a fast-paced environment
  • Ability to effectively collaborate effectively in a dynamic, cross-functional matrix environment
  • Outstanding communication skills (verbal and written)
  • A desire to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative
Job Responsibility
Job Responsibility
  • Supporting the development and execution of regulatory strategy for assigned programs in the EU and international markets in collaboration with Global Regulatory Leads, Regional Regulatory Strategists, and Country Regulatory Leads
  • Preparing and contributing to regulatory submissions including Scientific Advice meeting requests, briefing documents, clinical trial applications, orphan drug designations, pediatric plans, expedited pathway applications, DSURs, and marketing authorization applications (MAA)
  • Coordinating aspects of regulatory submissions relevant to the assigned program(s), ensuring alignment with global strategy and timelines
  • Supporting regulatory interactions with the EMA and other international health authorities
  • Engaging with cross-functional regulatory teams to ensure consistency, compliance, and strategy execution
  • Identifying, assessing, and managing regulatory risks associated with assigned program(s)
  • Tracking, following up, and archiving correspondence, regulatory commitments, and queries from EMA and international agencies
  • Working independently and collaboratively in matrixed project teams to achieve program goals
  • Applying critical thinking to anticipate potential regulatory hurdles and proactively address challenges specific to mRNA as a novel modality
  • Contributing to continuous improvement and innovation within regulatory processes
What we offer
What we offer
  • Best-in-class healthcare, plus voluntary benefit programs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right

Qualified Person

Joining Moderna offers the unique opportunity to be part of a pioneering team th...
Location
Location
United Kingdom , Oxford
Salary
Salary:
Not provided
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A Life Science degree and/or relevant postgraduate qualification, with a minimum of 10 years’ experience in quality roles within the biotechnology and/or pharmaceutical industry
  • Eligibility to act as a Qualified Person (QP), with demonstrable knowledge of biologics and sterile manufacturing sufficient to be named on the site’s licences issued by the MHRA
  • Commitment to maintaining QP status through ongoing Continuing Professional Development
  • Experience working in GMP-regulated pharmaceutical / biological manufacturing environments
  • Expert knowledge of Pharmaceutical Quality Management Systems, including their application across the product lifecycle
  • Extensive understanding of GxP requirements for both early-phase clinical trial materials and commercial products, including interpretation and application of EU GMP and associated MHRA guidance
  • Demonstrated, in-depth understanding of broader GMP principles, industry standards, and current trends shaping the regulatory landscape
  • Experience as a qualified pharmaceutical auditor (internal and/or external)
  • Proven experience hosting and participating in regulatory inspections (e.g., MHRA, FDA, EMA)
  • Demonstrated ability to influence cross-functional teams, provide leadership and drive organisational change.
Job Responsibility
Job Responsibility
  • Acting as the named Qualified Person (QP) on Moderna’s site licence(s)
  • Certifying and authorising batch releases in full compliance with The Human Medicines Regulations 2012, EU GMP (Annex 16, and where applicable, Annex 13), and MHRA guidance
  • Ensuring sterile drug product batches meet cGMP, approved specifications, and the conditions of the Marketing or Clinical Trial Authorisation
  • Maintaining oversight of the PQS as it pertains to QP responsibilities, ensuring it is fit for purpose
  • Escalating GMP or product quality concerns related to safety and efficacy to senior leadership
  • Participating as a member of the site and country Quality teams, promoting strong quality culture and QRM principles
  • Attending and reporting at the Quality Management Review Forum
  • Overseeing delegated activities and ensuring proper training of personnel or third parties
  • Leading or participating in self-inspections, external audits, and Quality Risk Assessments
  • Serving as the QP point of contact for Technical/Quality Agreement reviews and approvals
What we offer
What we offer
  • Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Fulltime
Read More
Arrow Right

Director, Clinical Pharmacology

The role is positioned in the Clinical Pharmacology group, Clinical and Quantita...
Location
Location
United States , Cambridge
Salary
Salary:
167000.00 - 300700.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD and/or PharmD in Clinical Pharmacology, Pharmacometrics, Pharmaceutics, Statistics, Engineering, or a related field with a minimum of 8-10 years of industry experience in clinical pharmacology
  • In depth knowledge of clinical pharmacology, PK/PD principles, modeling and simulation, ADME and quantitative translational sciences
  • Hands-on quantitative skills, modeling expertise and familiarity with clinical operations and translational sciences
  • Sound knowledge of drug regulatory authority biopharmaceutics and clinical pharmacology requirements to support the clinical development and marketing of new drug products
  • Drug development experience in oncology and rare diseases preferred
  • expertise in immune therapeutics and/or infectious diseases is a plus
  • Platform expertise in mRNA therapeutics, and/or experience with biologics and new modalities preferred
  • Demonstrated ability to work independently, lead functional initiatives, adapt quickly and collaborate effectively in a highly dynamic environment and influence cross-functional teams
  • Proficient in using pharmacokinetic, modeling and data visualization software (e.g. Phoenix WinNonlin, R, Monolix, NONMEM, etc)
  • Outstanding verbal and written communication skills, with the ability to distill complex data for diverse audiences
Job Responsibility
Job Responsibility
  • Develop a fit-for-purpose Clinical Pharmacology development plan, including dose selection and optimization, evaluation plan for special populations, PK/PD and immunogenicity assessment, and pediatric development
  • Collaborate with program teams to develop dose selection strategy and support decision makings for first-in-human studies and IND submissions
  • Represent CQP in a highly matrixed team setting to drive study execution and operational excellence toward product development goals
  • Lead the development of CQP related sections in regulatory documents (e.g., clinical protocols, INDs, regulatory meeting briefing books, summary documents for BLAs, responses to regulatory authorities) and represent clinical pharmacology in regulatory interactions
  • Lead/oversee the Clin Pharm data analysis, interpretation, and reporting to inform clinical implications and development decisions
  • Advocate and represent clinical pharmacology and MIDD strategies with internal and external stakeholders
  • Mentor junior team members to contribute to the development of a high-performing Clinical Pharmacology team
  • Leverage literature data and collaborate with external consultants, CRO partners and academic sites to problem solve and develop solutions to clinical pharmacology issues and grow organizational knowledge on mRNA platform
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Annual discretionary bonus, other incentive compensation, or equity award
  • Fulltime
Read More
Arrow Right

Senior Director, Clinical Development, Oncology

Moderna is seeking an experienced oncology drug developer lead Clinical Developm...
Location
Location
United States , Cambridge, Massachusetts; Princeton, New Jersey
Salary
Salary:
210900.00 - 379200.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with relevant hematology and/or oncology in an academic or hospital environment
  • Experience in oncology drug development demonstrated by at least 3 years in the biopharmaceutical industry
  • In exceptional cases, at least 5 years of experience as an early-phase clinical trialist in academia would be considered
  • Medical oncology and/or hematology fellowship training is preferred
  • Experience in oncology and/or hematology immunotherapeutics is preferred
  • Experience in conducting translationally rich oncology and/or hematology clinical trials is highly valued
  • Demonstrated track record in leading cross-functional teams and work streams (e.g., translational medicine, biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences)
  • Outstanding verbal and written communication skills, in addition to excellent organizational skills
  • Understanding of the entire drug development process, including clinical and non-clinical study design and execution
  • Thorough understanding of clinical research methodology and biostatistics principles, to facilitate innovative and efficient clinical trial design, and clinical development plans with clear data-driven decision rules
Job Responsibility
Job Responsibility
  • Collaborate in the development and execution of the Clinical Development Plan (CDP) for assigned oncology assets
  • Integrates scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP
  • Generates data and evidence required to determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe
  • Establishes expeditious clinical development timelines, incorporating key decision points and Go/No Go criteria for the CDP
  • Collaborate effectively with program counterparts in Translational Medicine, Pharmacometrics, Research, Biostatistics, Clinical Operations, Regulatory, Commercial, and other functional areas as needed
  • Contributes to and partners with the development of strategic initiatives, such as organizational initiatives within Clinical Development
  • Plays an active role in the technical and leadership development of Clinical Scientists
  • Employs visioning and strategic thinking to provide expert leadership of disease/therapeutic area specific strategy for a drug(s) or program(s)
  • Leads selected clinical development projects for products/franchise of compounds
  • Able to lead and influence across a diverse range of scientific external experts (e.g. regulators, payors, CROs, consultants, investigators) in order to deliver integrated clinical development strategy, which align to the business strategy and achieves mutual goals related to patient need
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Eligible for an annual discretionary bonus, other incentive compensation, or equity award
  • Fulltime
Read More
Arrow Right