CrawlJobs Logo

Senior Medical Editor

pharmagenesis.com Logo

Oxford PharmaGenesis

Location Icon

Location:
United Kingdom , Oxford

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

Oxford PharmaGenesis is looking for a meticulous Senior Medical Editor to join our editing team on a 12-month fixed-term contract. This is a hybrid role based in our Oxfordshire office. You will ideally have previous experience of editing scientific publications and will be comfortable working with both print and digital deliverables. This is a great opportunity to join a close-knit, supportive editorial team and to work with talented writing, account management and artwork colleagues on a wide variety of project types.

Job Responsibility:

  • Edit a diverse range of scientific materials, including patient-focused materials, manuscripts, abstracts, presentations, posters and digital outputs, in adherence with the relevant style guides
  • Conduct thorough proofreading, including detailed checks of typeset layouts and figure redraws, as well as journal proofs
  • Create and update account-specific style guides as needed
  • Collaborate closely with colleagues to help ensure that projects are delivered on time and to budget
  • Attend project and team meetings, helping to shape workflows, promote best practice and adapt to client needs

Requirements:

  • Science, English or related bachelor’s degree
  • Previous experience in healthcare communications or journal publishing
  • Proficiency in Microsoft Word and PowerPoint, Adobe Acrobat and reference management software, such as EndNote (not essential)
  • Exceptional eye for detail and a strong command of English
  • Service-oriented approach, with the ability to work on multiple projects simultaneously
  • Strong time management and communication skills
What we offer:
  • Exceptional learning opportunities
  • Truly inclusive environment
  • Matched charitable fundraising
  • Support for charities working towards the betterment of health, society and/or people
  • Hybrid working approach

Additional Information:

Job Posted:
March 18, 2026

Employment Type:
Fulltime
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 Senior Medical Editor

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

Associate Creative Director, Copy

We are looking for an Associate Creative Director (Copy) who is a master of lang...
Location
Location
United States , Cary; New York; Philadelphia
Salary
Salary:
130000.00 - 155000.00 USD / Year
inizioevoke.com Logo
Inizio Evoke
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master copywriter with proven ability to craft impactful and compliant messaging across multiple channels
  • Inspiring leader and mentor passionate about fostering talent
  • Strategic thinker who understands how copy influences brand positioning, engagement, and behavior change
  • Highly skilled in adapting tone and voice for various audiences including healthcare professionals, patients, and caregivers
  • Meticulous editor ensuring clarity, accuracy, and alignment with regulatory and brand guidelines
  • Collaborative partner who enjoys working with designers, strategists, and account leads
  • Continuous learner staying updated on industry trends, regulations, and best practices
  • Professional, with integrity, and enthusiasm
Job Responsibility
Job Responsibility
  • Be the brand voice expert ensuring consistency across all written materials
  • Mentor a team of Copywriters and Senior Copywriters
  • Create and refine messaging strategies
  • Collaborate closely with Art, Strategy, and Medical teams
  • Oversee development of messaging platforms across digital, print, social, and video
  • Navigate and apply regulatory requirements
  • Present and defend creative work to clients, regulatory teams, and internal stakeholders
  • Stay ahead of industry trends
What we offer
What we offer
  • Fully remote work environment
  • Competitive compensation
  • Company-paid medical
  • Company-paid dental
  • 401(k)
  • Tuition reimbursement
  • Flexible time off
  • Fulltime
Read More
Arrow Right

Senior Full-Stack Engineer

Building infrastructure for machine learning training data quality. Platform han...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
encord.com Logo
Encord
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in building complex UIs
  • Experience developing and maintaining multiple systems from scratch
  • Knowledge of trade-offs in building reliable, performant software
  • Open to learning new technologies
  • Passionate and eager to learn
Job Responsibility
Job Responsibility
  • Build out editor interface for visualising and annotating data
  • Handle wide range of data modalities (image, video, audio, text, PDFs, medical images, LIDAR)
  • Render complex 3D/4D scenes with thousands of objects
  • Combine data from several modalities while maintaining high browser performance
  • Take end-to-end ownership of projects from product, design and architectural decisions to deployment, monitoring and measuring impact
  • Work across the stack
What we offer
What we offer
  • Competitive salary and equity
  • 25 days annual leave + public holidays
  • Opportunities for growth in hyper growth business
  • Work at cutting edge of computer vision and deep learning
  • Explore enterprise AI use cases across multiple industries
  • Fulltime
Read More
Arrow Right

Senior Art Director

The Senior Art Director is responsible for partnering with internal teams and cl...
Location
Location
United States , West Chester
Salary
Salary:
Not provided
synchronygroup.com Logo
Synchrony Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in Visual Communication, Graphic Arts, or a related course of study is preferred
  • Minimum of 5 years of advertising agency experience, preferably in Pharmaceuticals
  • In-depth knowledge of Adobe Creative Cloud, Sketch, Figma and Microsoft Office Suite
  • Strong understanding of printing process (spec sheets, dieline reviews, mechanicals, printers proofs) and ability to own the layout of a print piece until completion
  • Working knowledge of interactive programming to allow for thoughtful digital UX/UI design best practices
  • Skilled to think in abstract terms
  • can make connections between unrelated ideas
  • can formulate innovative concepts
  • Ability to tell compelling stories through visuals that connect with audiences across multiple channels and drives customer engagement in support of brand strategy
  • Strong creative design, conceptual skills, and knowledge in website design systems
Job Responsibility
Job Responsibility
  • Engage with clients to understand their brand(s), key messages, and creative vision to turn complex insights, data, and messages into compelling stories for a variety of audiences, including patients and healthcare professionals
  • Collaborate with internal departments, such as creative, accounts, project management, medical, and editorial
  • Obtain an understanding of the therapeutic area, competitive landscape and target audience of the products they manage
  • Conceptualize and brainstorm innovative brand experiences and maintain the consistency of brands across all marketing materials
  • Assist Account Services in the creation of the Strategic Alignment Brief and ensure that all projects under this brief are consistently upholding the strategy
  • Develop brand style guidelines and ensure internal teams and external partners stay compliant
  • Collaborate and manage outside vendors (printers, photographers, video editors, writers, designers, PowerPoint specialists and illustrators) to ensure quality deliverables and adherence to timeline
  • Design solutions that go beyond what is expected
  • Partner with copywriters to establish or evolve ideas, create sketches or storyboards that convey relevant concepts
  • Track and synthesize competitive brand creative, share and utilize best practice examples
What we offer
What we offer
  • competitive salaries
  • generous paid time off
  • excellent health insurance
  • family leave
  • a 401(k) plan with employer matching
  • Fulltime
Read More
Arrow Right
New

Title Clerk

We are looking for a highly organized and service-driven individual with strong ...
Location
Location
United States , Fort Lauderdale
Salary
Salary:
Not provided
https://www.roberthalf.com Logo
Robert Half
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Previous experience in a title company, escrow office, real estate legal setting, or similar closing environment is preferred
  • Hands-on familiarity with Qualia is strongly preferred
  • Proficiency with Microsoft Outlook and standard office applications is required
  • Strong attention to detail with the ability to organize and prioritize a high volume of active files
  • Ability to manage several transactions at once while meeting deadlines in a fast-paced environment
  • Effective verbal and written communication skills with a client-focused approach
  • Detail-oriented, reliable, and collaborative work style
  • Bilingual fluency in English and Spanish is required
Job Responsibility
Job Responsibility
  • Manage title and closing files from initial intake through post-closing completion, keeping documentation accurate and up to date
  • Request and follow up on payoffs, estoppel letters, lien searches, recording packages, and other items needed to move transactions forward
  • Communicate with lenders, real estate agents, attorneys, buyers, sellers, and association representatives to coordinate file progress and resolve outstanding matters
  • Review title commitments and related documentation, then assist in addressing conditions or issues that could delay closing
  • Support post-closing activities by handling disbursements, submitting documents for recording, and monitoring final file completion
  • Track deadlines and recording status to help ensure each transaction is finalized correctly and within expected timeframes
  • Provide scheduling assistance, client updates, and general administrative support to maintain an efficient office workflow
  • Maintain well-organized digital records and transaction files to support compliance, accuracy, and easy retrieval of information
What we offer
What we offer
  • medical
  • vision
  • dental
  • life and disability insurance
  • 401(k) plan
  • free online training
  • Fulltime
Read More
Arrow Right
New

Temporary File Digitization Project Assistant

A company transitioning to a paperless environment is seeking a detail-oriented ...
Location
Location
United States , Miami Beach
Salary
Salary:
Not provided
https://www.roberthalf.com Logo
Robert Half
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Previous administrative, clerical, or data entry experience preferred
  • Strong attention to detail and organization skills
  • Comfortable working with scanners, computers, and Microsoft Office
  • Ability to work in a fast-paced environment and meet deadlines
  • Reliable and able to start immediately
Job Responsibility
Job Responsibility
  • Scan and digitize paper files and documents
  • Organize electronic records and folders accurately
  • Upload and index files into the company database/system
  • Review documents for completeness and quality control
  • Maintain confidentiality of sensitive information
  • Assist with general clerical and administrative support as needed
What we offer
What we offer
  • medical
  • vision
  • dental
  • life and disability insurance
  • 401(k) plan
Read More
Arrow Right
New

Pharmacy Intern

You’ve invested a lot of time and energy in your education. Now you want the cha...
Location
Location
United States , Fort Lauderdale
Salary
Salary:
Not provided
https://www.cvshealth.com/ Logo
CVS Health
Expiration Date
May 28, 2026
Flip Icon
Requirements
Requirements
  • Accepted into, or actively enrolled in, an ACPE accredited college or school of pharmacy
  • Must possess, or be in the process of obtaining, valid intern and/or technician licensure as required
Job Responsibility
Job Responsibility
  • Completion of a comprehensive training roadmap, focusing on Key Learning Experiences (KLEs) that build aptitude
  • Living our purpose by following all company SOPs at each workstation
  • Following pharmacy workflow procedures at each pharmacy workstation for safe and accurate prescription fulfillment
  • Contributing to positive patient experiences showing empathy and genuine care
  • Offering to counsel, fielding medical questions, and soliciting information on a patient’s medical history
  • Taking telephonic prescriptions from the prescriber, and calling the prescriber to clarify prescriptions
  • Maintaining the highest level of self-awareness and providing in-the-moment coaching, training, and mentoring to pharmacy team members
  • Completing basic inventory activities
  • Contributing to a high-performing team
  • Remaining flexible for both scheduling and business needs
  • Fulltime
Read More
Arrow Right