CrawlJobs Logo

Assistant Editor - Life Sciences

mdpi.com Logo

MDPI

Location Icon

Location:
Switzerland , Basel

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

Kickstart your career in academic publishing! Join MDPI in Basel as an Assistant Editor, support global researchers, and help make science accessible. Recent graduates in Life Sciences welcome! To grow and strengthen our Editorial team at the Headquarter of MDPI, we are looking for recent graduates who are eager to stay engaged with academia and contribute to making scientific research widely accessible by helping researchers worldwide publish their latest results.

Job Responsibility:

  • Support the editorial process for academic research journals in your domain of expertise
  • Organize the peer review process for submitted manuscripts and coordinate editorial decisions
  • Be in charge of formatting manuscripts according to our in-house standards
  • Handle email communication between all parties involved in the publication process
  • Ensure that scholarly articles are accurately edited and published with a high degree of consistency and within the deadlines
  • Serve as key point of contact between the Editorial Office and external authors and readers

Requirements:

  • A Master’s, or PhD degree in one of the following fields: Molecular Science, Biodiversity, Biology, Microbiology, Medicine, Pharmacy, Ecology and Life Science
  • Excellent written and spoken English skills
  • Advanced knowledge of MS Office applications (Word, Excel, PowerPoint)
  • Passion for scientific research and academic publishing
  • Team player with the capability to work in a dynamic, international environment
  • Detail-oriented with the capacity to see the big picture
  • Strong organizational and time management skills
  • Very good communication and coordination skills

Nice to have:

  • Fluent German would be plus
  • Professional experience with scholarship publishing is an advantage
  • Experience in creating presentations and writing is an asset
  • A familiarity with the academic editorial process is an advantage
What we offer:
  • The opportunity to contribute to the academic/scientific community
  • Flexible working hours
  • Team bond strengthening through team-building events
  • Professional growth opportunities with our global training system
  • Working in a collaborative and socially responsible team
  • Company retreat facility
  • Full-coverage insurance for accidents/daily sickness
  • Prime location near Basel train station and city center

Additional Information:

Job Posted:
December 10, 2025

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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

Briefcase Icon

Similar Jobs for Assistant Editor - Life Sciences

Assistant Editor - Medical Sciences

Kick-start your career in academic publishing: join MDPI in Basel as an Assistan...
Location
Location
Switzerland , Basel
Salary
Salary:
Not provided
mdpi.com Logo
MDPI
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s or PhD degree in one of the following fields: Medicine, Clinical Sciences, Pharmacy, Biomedical Sciences, or related health- and life-science fields
  • Excellent written and spoken English skills
  • Advanced knowledge of MS Office applications (Word, Excel, PowerPoint)
  • Passion for scientific research and academic publishing
  • Team player with the capability to work in a dynamic, international environment
  • Detail-oriented with the capacity to see the big picture
  • Strong organizational and time management skills
  • Very good communication and coordination skills
Job Responsibility
Job Responsibility
  • Support the editorial process for academic research journals in your domain of expertise
  • Organize the peer review process for submitted manuscripts and coordinate editorial decisions
  • Be in charge of formatting manuscripts according to our in-house standards
  • Handle email communication between all parties involved in the publication process
  • Ensure that scholarly articles are accurately edited and published with a high degree of consistency and within the deadlines
  • Serve as key point of contact between the Editorial Office and external authors and readers
What we offer
What we offer
  • Flexible working hours
  • Team bond strengthening through team-building events
  • Professional growth opportunities with our global training system
  • Working in a collaborative, diverse, and socially responsible team
  • Company retreat facility
  • Full-coverage insurance for accidents/daily sickness
  • Prime location near Basel train station and city center
  • Fulltime
Read More
Arrow Right

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...
Location
Location
United States
Salary
Salary:
142100.00 - 159500.00 USD / Year
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
  • Experience writing, reviewing, or editing protocols and clinical study reports required
  • Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
  • Experience writing, reviewing, or editing regulatory briefing books preferred
  • Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
  • Ability to interpret and create complex tabular and graphical clinical data presentations
  • Advanced applied knowledge of basic clinical laboratory tests
  • Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
  • Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
  • Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection
Job Responsibility
Job Responsibility
  • Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
  • Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
  • Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
  • Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
  • Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
  • Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
  • Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
  • Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
  • Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
  • Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
What we offer
What we offer
  • Discretionary annual bonus
  • Discretionary stock-based long-term incentives (eligibility may vary based on role)
  • Paid time off
  • Company-sponsored medical, dental, vision, and life insurance plans
  • Fulltime
Read More
Arrow Right

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...
Location
Location
United States , San Rafael
Salary
Salary:
116000.00 - 159500.00 USD / Year
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
  • Experience writing, reviewing, or editing protocols and clinical study reports required
  • Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
  • Experience writing, reviewing, or editing regulatory briefing books preferred
  • Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
  • Ability to interpret and create complex tabular and graphical clinical data presentations
  • Advanced applied knowledge of basic clinical laboratory tests
  • Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
  • Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
  • Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection
Job Responsibility
Job Responsibility
  • Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
  • Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
  • Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
  • Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
  • Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
  • Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
  • Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
  • Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
  • Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
  • Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
What we offer
What we offer
  • Discretionary annual bonus
  • Discretionary stock-based long-term incentives
  • Paid time off
  • Company-sponsored medical, dental, vision, and life insurance plans
  • Fulltime
Read More
Arrow Right

Medical Writer

The Medical Writer applies basic to intermediate documentation preparation and d...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or higher degree preferred
  • scientific focus desirable
  • University-level medical or technical writing course(s) or equivalent experience in science/technical writing
  • Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
  • Up to 2 years as a medical writer in the pharmaceutical industry or at least 5 years of medical or scientific writing experience as a primary job responsibility
  • Familiar with drug development process (discovery to market)
  • Basic understanding of biostatistical and clinical research concepts
  • Basic applied knowledge of documentation required for the conduct of clinical studies, protocol design, study results reporting
  • Writing high-quality documents that support corporate goals and objectives
  • Experience writing, reviewing, or editing protocols and clinical study reports preferred
Job Responsibility
Job Responsibility
  • Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
  • Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
  • Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
  • Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
  • Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
  • Assists in developing and reviewing standard processes and templates within Global Medical Writing
  • Works effectively with cross-functional groups within BioMarin
  • Other tasks as assigned
  • Fulltime
Read More
Arrow Right

Medical Writer

The Medical Writer 1 applies basic to intermediate documentation preparation and...
Location
Location
United States , San Rafael
Salary
Salary:
74100.00 - 100000.00 USD / Year
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or higher degree preferred
  • scientific focus desirable
  • University-level medical or technical writing course(s) or equivalent experience in science/technical writing
  • Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association
  • Up to 2 years as a medical writer in the pharmaceutical industry OR At least 5 years of medical or scientific writing experience as a primary job responsibility
  • Familiar with drug development process (discovery to market)
  • Basic understanding of biostatistical and clinical research concepts
  • Basic applied knowledge of documentation required for the conduct of clinical studies
  • Basic applied knowledge of protocol design
  • Basic applied knowledge of study results reporting
Job Responsibility
Job Responsibility
  • Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
  • Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
  • Aids in managing study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
  • Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
  • Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
  • Assists in developing and reviewing standard processes and templates within Global Medical Writing
  • Works effectively with cross-functional groups within BioMarin
  • Other tasks as assigned
What we offer
What we offer
  • discretionary annual bonus
  • discretionary stock-based long-term incentives
  • paid time off
  • company-sponsored medical, dental, vision, and life insurance plans
  • Fulltime
Read More
Arrow Right
New

Assistant Project Manager I

The Assistant Project Manager I (APM I) supports project managers in coordinatin...
Location
Location
United States , New Orleans
Salary
Salary:
Not provided
cecoconcrete.com Logo
Ceco Concrete Construction, LLC
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelors or Associates degree in Engineering, Construction Management, related degree, or its equivalent and a minimum of 1-2 years of work experience successfully supporting similar primary responsibilities meeting and exceeding performance expectations
  • Excellent communication and interpersonal skills with the ability to communicate effectively with all levels of the organization, as well as with customers and vendors
  • Detail oriented with the ability to efficiently analyze and organize significant amounts of information regarding plan layouts, material deliveries and jobsite productivities
  • Proficient with Microsoft Office Suite (Word, Excel, and Outlook)
  • Advanced knowledge of safety and relevant OSHA requirements and regulations
  • Ability to travel and work for extended period of time on projects outside of office area
Job Responsibility
Job Responsibility
  • Coordinates the planning and implementation of concrete frame and formwork projects
  • Performs jobsite inspections/audits of shoring, rebar/pt installation, safety, and quality
  • Responsible for assisting the managing of project productivity, costs, quality and safety consistent with company policies and practices
  • Develops and maintains customer relationships to enhance company's ability to procure projects, reduce risk, and ensure operational efficiency
  • Creates and coordinates material and equipment schedules and promotes their efficient use
  • Coordinates all subcontractor and vendor contracts and associated processes and procedures
  • Performs special projects and completes all other duties as assigned or requested for the general support of the organization
What we offer
What we offer
  • Inclusive Medical, Dental, Vision, Accident, and Illness insurance
  • Company paid Disability and Life insurance
  • Health Savings Account contribution of up to $1,000 per year
  • 401(k) retirement savings program with a company match
  • Employee Assistance Program including discounts with major vendors & products
  • Mental and physical wellness programs
  • Competitive time off package including vacation, sick, and holiday pay
  • Career advancement opportunities with a stable well-established organization
  • Tuition reimbursement program and access to LinkedIn Learning course
  • Fulltime
Read More
Arrow Right
New

Long Term Supply Teacher

Inspire the leaders of tomorrow by joining our dynamic teaching community dedica...
Location
Location
United Kingdom , Gatwick
Salary
Salary:
Not provided
https://www.randstad.com Logo
Randstad
Expiration Date
May 22, 2026
Flip Icon
Requirements
Requirements
  • Full teaching responsibilities within your placement
  • Flexibility - placements need not always be 5 working days
  • job shares considered
  • Comprehensive working history and two recent working references
  • Marking, planning, and teaching throughout extended periods
  • Payment to scale for placements surpassing 6 weeks
  • Full-time availability dedicated to teaching
  • QTS/PGCE qualification required
  • driving preferred for varied school locations
  • Two work references
Job Responsibility
Job Responsibility
  • Full teaching responsibilities within your placement
  • Marking, planning, and teaching throughout extended periods
What we offer
What we offer
  • Refer a friend bonus scheme
  • Unlock a £300 Refer a Friend bonus for additional rewards
  • Weekly pay with competitive daily rates
  • Simple hour submissions through our user-friendly app
  • A dedicated consultant deeply rooted within schools
  • Personalised assistance for compliance and seamless onboarding
  • Fulltime
Read More
Arrow Right
New

Program Specialist - Identity Operations & Insights

Operations & Insights manages day-to-day performance and delivery—driving qualit...
Location
Location
Taiwan (ROC) , Taipei City
Salary
Salary:
Not provided
uber.com Logo
Uber
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 2 years of experience in operations management and managing cross-functional projects
  • Experience working in Google Sheets / Excel. Advanced technical experience working with spreadsheets, Dashboards and graphs, pivot tables to identify qualitative and quantitative insights, and break down information into clear, actionable recommendations
  • comfortable interpreting reports and using tools like Excel/Google Sheets, Tableau, or similar platforms to support decision-making
  • Strong organizational and planning skills in order to manage several tasks
  • Ability to prioritize, create plans and complete tasks on your own. Demonstrated ability to operate independently, prioritize effectively, and push initiatives forward without needing day-to-day oversight.
Job Responsibility
Job Responsibility
  • Support and monitor the document operations for global and APAC
  • making sure multiple teams have all tools and information required to meet quality and productivity targets. Monitor our Identity scorecards, dashboards, and audit cadences to track operations and drive accountability
  • Analyze data, with the help of our dashboards and queries, you will monitor Docs operations, understand the main challenges and look for ways to improve it (policies, processes, agent training, tooling, etc)
  • Execute cross-functional project plans that help us improve our quality and efficiency ensuring deadlines are mean, designing the SOPs to make sure we are supporting Identity Program requirements
  • Create or improve existing processes through data analytics, footprint migrations, processes and policy updates and roll outs, reporting improvements, process standardization and keeping track of plans, quality and timelines for such activities
  • Own the feedback loop across teams for Docs Operations in EMEA with the regional BPOs/COEs, designing effective ways to identify roadblocks or issues in the rollout and implementation of policies and processes as well as provide solutions to address those
  • Estimate work efforts, define milestones and manage resources accordingly, while driving adherence and compliance with deadlines on deliverables
  • Track progress, understand dependencies, communicate status to upper management and stakeholders, and facilitate and coordinate schedules for different local or regional requests
  • Proactively work to remove obstacles and enable forward momentum and progress. Manage issue escalations and provide support to teams balancing competing priorities
  • You will also need analytical skills to be able to solve problems that may come up during a typical workday. You will be analyzing data and making decisions regarding operations and processes on a regular basis.
  • Fulltime
Read More
Arrow Right