Reviewer - Biology Job at Atomi

Scientific Coding Research Specialist

We are hiring highly analytical and computationally proficient researchers acros...

Location

India , Noida

Salary:

Not provided

AquSag Technologies

Expiration Date

Until further notice

Requirements

PhD or PhD candidate in Computational Physics
At least one peer-reviewed publication
Advanced proficiency in Python for scientific coding
PhD or PhD candidate in Computational Biology or Bioinformatics
At least one peer-reviewed publication
Advanced Python skills for modelling or biological computation
PhD or PhD candidate in Computational Mathematics
At least one peer-reviewed publication
Advanced Python skills for numerical methods or algorithmic computation
PhD or PhD candidate in Computational Chemistry

Job Responsibility

Develop original, research-grade or graduate-level scientific problems in your domain
Use Python for scientific coding, modelling, simulation or analytical computation
Define problem categories, secondary tags and difficulty levels clearly
Solve all formulated problems rigorously, ensuring methodological precision, reliability and coherent reasoning
Participate in two-tier review cycles to evaluate accuracy of problems and solutions
Review peer submissions with a focus on scientific correctness and internal consistency
Incorporate feedback promptly and refine content to maintain high quality standards
Work closely with reviewers and team leads to uphold overall technical excellence

Assistant Editor

Help researchers worldwide publish their findings! Join us as an Assistant Edito...

Location

Singapore , Singapore

Salary:

Not provided

MDPI

Expiration Date

Until further notice

Requirements

Master's degree in Biology, Chemistry, Engineering, Physics, Computer Science, Materials Science, Agriculture, Medicine and Pharmacy, Ecology and Environmental Sciences, Social Sciences, Humanities, Linguistics, Education Science etc.
Advanced knowledge of MS office applications (Word, Excel, PowerPoint)
Strong English skills in written and spoken language
Ability to multi-task, attention to detail
Organizational and time management skills
Strong communication and coordination skills
Prior research and/or lab experience in relevant academic fields

Job Responsibility

Support the editorial process for academic research journals in your domain of expertise
Organize peer review for submitted manuscripts and coordinate editorial decisions
Handle email communication between the parties involved in the publication process
Collaborate with other members of the editorial team and production team
Ensure that scholarly articles are accurately edited and published according to tight deadlines with a high degree of consistency

What we offer

Professional and personal development
International work environment
Flexible working hours in the limits of a full-time job
Trips to the other MDPI offices
Attending Scientific Conferences
Competitive salary, benefits

Fulltime

Plant Health Researcher Assistant

Would you be interested in joining the European Food Safety Authority (EFSA) as ...

Location

Italy , Parma

Salary:

28000.00 - 34000.00 EUR / Year

Randstad

Expiration Date

January 27, 2026

Requirements

Excellent knowledge of English (at least C1 level)
Previous experience in literature research and reviews
Academic background in Plants Health, Plants Biology and/or related areas
Behavioural competencies: working with others, analysis and problem solving, drive for results, good level of autonomy

Job Responsibility

Update pest reports
Conduct literature searches focusing on: Plant pests
Host plants of the pests
Available detection methods and identification methods survey cards
Integrate acquired knowledge into official documentation

Fulltime

Clinical Genomics Scientist, Oncology

BillionToOne is looking for a Clinical Genomics Scientist, Oncology to help driv...

Location

United States , Menlo Park

Salary:

158401.00 - 179521.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Ph.D. in Human Genetics, M.S. in Genetic Counseling, or related field
2+ years of experience in somatic variant interpretation based on ACMG/AMP guidelines in a clinical setting (alternatively, 1+ years of germline variant interpretation and 1+ years of somatic variant interpretation experience)
Hands-on experience working with human mutation databases (COSMIC, ClinVar, OncoKB), functional annotation sources (dbSNP), and genome browsers (UCSC)
Familiarity with IGV and BAM file analysis and data-minded willingness to learn to use basic bioinformatics tools, with technically minded insights
Knowledge of cancer somatic mutation and signaling pathways (e.g., which mutations have FDA approved drugs, Phase II/III clinical trials, which mutations are considered “hot targets” for drug development, etc.)
Exceptional attention to detail to follow highly detailed SOPs and strong organizational skills to track and manage clinical reporting and product improvement projects
Excellent communication skills and ability to work collaboratively with cross-functional teams
Operationally-defined flexible schedule, including weekends, as dictated by clinical reporting needs

Job Responsibility

Somatic variant interpretation and data review: Perform somatic-based variant interpretation, diving into the literature and databases to classify variants and match treatments for reporting, performing verification as required with BAM file analysis
Clinical report drafting: Carefully draft reports for each requisition primarily using in-house reporting API, working closely with the engineering and QA teams on reporting, and the laboratory directors on report language
Somatic mutation interpretation and reporting policy development: Work closely with lab directors, R&D, medical, and other related functions to develop and modify the somatic interpretation SOPs in accordance with ACMG/AMP guidelines, and the latest published literature
Content curation: Contribute to curation of gene-level content such as domain and critical residue curation
Molecular tumor board: Serve as a subject matter expert in consulting with the medical science liaison team, and presenting in molecular tumor boards to facilitate knowledge sharing
Contribute to oncology R&D: Work closely with the R&D team to help with somatic oncology based projects, providing expertise on variant interpretation, biological pathways/mechanisms, and other gene/variant-level reviews and analyses

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Senior–Principal Botanist

We have an opportunity for a Senior to Principal level Botanist to join our Biol...

Location

Australia , O’Connor, WA

Salary:

Not provided

Focused Vision Consulting

Expiration Date

Until further notice

Requirements

Bachelor degree (minimum) in botany, ecology, biological science, environmental science or equivalent
5+ years’ relevant experience (in flora and vegetation assessments, preferably in Western Australia)
demonstrated familiarity with current Technical Guidance for flora and vegetation surveys
willingness to travel for field assessments, including to remote locations
experience in the preparation of, or contributions to technical biological assessment reports
the ability to lead and manage teams and projects
current Western Australian C-class driver’s licence
proven experience in managing client relationships
excellent verbal and written communication skills
a proactive attitude and commitment to delivering exceptional results in a team-focused environment

Job Responsibility

Lead and contribute to botanical and ecological projects
Study scoping and design
Leading field surveys, including in remote and exciting locations
Vegetation/GIS mapping and related spatial data management
Technical reporting of biological assessments and monitoring
desktop and field results
Report technical review
Aid in maintaining and strengthening client relationships
Collaborate with technical specialists in our Environmental Assessments and Management team
Play a vital role in developing and navigating strategic pathways of the business

What we offer

Competitive salary packages based on experience
Reward and recognition that goes well-beyond salary, including an established Employee Benefit Package
Opportunities to work on impactful projects
An outstanding, collaborative and supportive workplace culture, dedicated to quality, integrity and fun!
Professional development and career progression pathways

New

QA Clinical Supplies Specialist

Piper Companies is currently looking for an experienced QA Clinical Supplies Spe...

Location

United States , West Point

Salary:

38.00 - 43.00 USD / Hour

Piper Companies

Expiration Date

Until further notice

Requirements

2+ years of relevant experience in pharmaceutical/biotech industry or supply chain
Quality mindset with background in GMP record review
Self-driven, and capable of working independently
Experience within biologics and/or vaccines
Strong understanding of SAP, Trackwise, Midas, Veeva, and QMAS is preferred
Bachelor’s degree in related field preferred

Job Responsibility

Electronic batch record review of finished clinical goods to ensure clinical supplies are incompliance with cGMP and SOPs
Check clinical supplier specifications, labeling, storage, etc.
Review of Electronic records for regulatory submissions (IND or CTA)
Areas of focus will include biologics, vaccines, combination products, etc.

What we offer

Medical, Dental, Vision, 401K, PTO

Fulltime

Sr. Director, Clinical Scientist

The Sr. Director, Clinical Scientist plays a pivotal role in shaping the clinica...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Advanced degree (MS, Ph.D., Pharm.D., M.D., or equivalent) in a relevant scientific discipline preferred
7+ years of clinical development experience within biotech, pharmaceutical, or academic settings, with demonstrated leadership in advancing programs through early and late-stage development
Cell and gene therapy experience—particularly in CAR-T or T-cell–based modalities—strongly preferred
autoimmune disease experience highly desirable
Deep understanding of T-cell biology, immunology, and translational science principles relevant to cellular therapy
Proven ability to author and critically review clinical protocols, study reports, and regulatory documents, ensuring scientific integrity and compliance with ICH-GCP and global regulatory standards
Demonstrated skill in analyzing complex clinical data, conducting literature reviews, and synthesizing insights to inform program strategy
Exceptional scientific judgment, attention to detail, and analytical rigor
Strong communication and collaboration skills, with the ability to influence and partner effectively across cross-functional teams, investigators, and external experts
Highly organized with the ability to manage multiple priorities in a fast-paced, evolving environment.

Job Responsibility

Serve as the clinical science lead for assigned CAR-T programs, partnering with the Medical Director on the design, execution, and interpretation of clinical studies across all phases of development
Author and oversee key clinical documents — including protocols, amendments, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions (e.g., INDs, CTAs, DSURs, BLAs/MAAs)
Review, analyze, and interpret emerging clinical data (safety, efficacy, PK/PD) to identify trends and issues, ensuring timely resolution through cross-functional collaboration
Conduct literature and competitive landscape reviews to inform study design, data interpretation, and program strategy
Provide ongoing data review to ensure study conduct aligns with protocol, patient safety standards, and data integrity expectations
Collaborate with the Medical Monitor to ensure awareness of key safety and efficacy findings, supporting SAE review, narrative development, and safety governance activities
Lead or support governance activities, including preparation and presentation of materials for Development, Executive, and Scientific Steering Committees, as well as oversight of external boards (e.g., DSMB, adjudication committees)
Contribute to and present scientific and clinical data internally and externally (e.g., investigator meetings, scientific conferences, regulatory interactions)
Serve as the clinical science representative on cross-functional development and study teams, providing scientific and strategic input to ensure cohesive execution
Mentor study team members and contribute to vendor oversight to ensure consistency, quality, and scientific rigor across all clinical deliverables

What we offer

health and retirement, PTO, and stock option plans

Analytical Lab Manager

Maintain efficient operation as well as perform environmental monitoring, bacter...

Location

Salary:

Not provided

Avanos

Expiration Date

Until further notice

Requirements

Bachelor’s degree in laboratory technology, Microbiology, Biotechnology, Chemistry or related field
Advanced English level
Previous experience in microbiological testing, environmental monitoring or endotoxin testing (preferably within the medical device industry)
Knowledge of regulatory standards: ISO 13485 and FDA 21 CFR Part 820
Ability to follow standard operating procedures and interpret technical documents
Advanced knowledge of MS Office tools (Excel, Word and lab software)

Job Responsibility

Responsible to coordinate all environmental control activities for the facility, including certifications, and the periodic review of environmental monitoring results, as well as any tasks related environmental impact, change control and biological tests
Responsible to perform and maintenance the Biocontamination assessments for the product families
Ensure compliance with Standard Operating Procedures (SOPs)
Maintain required environmental and control conditions
Manage inventory of reagents, consumables, and equipment
Schedule and coordinate test execution
Supervise, train, and evaluate laboratory technical staff
Promote continuous training and a culture of compliance
Review and approve test records and reports
Investigate deviations or out-of-specification (OOS) results

Reviewer - Biology

Atomi

Location:
Australia

Category:
Education

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 22, 2025

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

Similar Jobs for Reviewer - Biology

Scientific Coding Research Specialist

Assistant Editor

Plant Health Researcher Assistant

Clinical Genomics Scientist, Oncology

Senior–Principal Botanist

QA Clinical Supplies Specialist

Sr. Director, Clinical Scientist

Analytical Lab Manager

Reviewer - Biology

Atomi

Location:Australia

Category:Education

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:December 22, 2025

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

Similar Jobs for Reviewer - Biology

Scientific Coding Research Specialist

Assistant Editor

Plant Health Researcher Assistant

Clinical Genomics Scientist, Oncology

Senior–Principal Botanist

QA Clinical Supplies Specialist

Sr. Director, Clinical Scientist

Analytical Lab Manager

Location:
Australia

Category:
Education

Contract Type:
Not provided

Job Posted:
December 22, 2025