Scientific Medical Writer Job at Randstad (Hyderabad)

Medical Writer, Scientific Communications

The Medical Writer, Scientific Communications is responsible for writing strateg...

Location

United States

Salary:

70000.00 - 85000.00 USD / Year

Vaniam Group

Expiration Date

Until further notice

Requirements

PhD in life sciences, MD, or PharmD
At least 1 year of work experience in an agency, the pharmaceutical industry, or a related scientific or medical writing position
Working knowledge of digital marketing
Commitment to ethical and transparent data dissemination standards
Demonstrated ability to work collaboratively in a dynamic team environment
Excellent interpersonal, organization, verbal, and written communication skills
Excellent quantitative and analytical skills and ability to synthesize complex or diverse information
Excellent problem-solving skills
Strong attention to detail and listening skills
Ability to meet tight deadlines and have excellent time management skills

Job Responsibility

Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials
Develop materials that are grammatically accurate and audience appropriate
Gain an understanding of the treatment landscape and strategic positioning of client products to help produce strategically aligned materials
Assess project needs and challenges
identify and implement solutions to meet productivity, quality, and client goals while maintaining compliance standards
Participate in client meetings and answer questions about projects when necessary
Build strong partnerships with and understand the importance of meeting the needs of internal teams
Work on multiple projects concurrently, prioritizing appropriately
Collaborate with team to execute project and meet deadlines
Emerging ability to assess areas for opportunity and improvement

What we offer

100% remote environment with opportunities for local meet-ups
Positive, diverse, and supportive culture
Investment in you with opportunities for professional growth and personal development through Vaniam Group University
Health benefits – medical, dental, vision
Generous parental leave benefit
Focused on your financial future with a 401(k) Plan and company match
Work-Life Balance and Flexibility
Flexible Time Off policy for rest and relaxation
Volunteer Time Off for community involvement
Emphasis on Personal Wellness

Fulltime

Scientific and Medical Writer

Job opportunity for a Scientific and Medical Writer M/F. Permanent position base...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Post-graduate science degree in a biomedical field
previous medical or scientific writing experience
ability to analyse and summarise data from a diverse range of indications
advanced scientific writing skills
experience in the preparation of marketing authorisation applications and regulatory responses would be advantageous
fluency in written and spoken English

Job Responsibility

medical writing of all types of regulatory and clinical study documentation including Investigators’ Brochures, clinical study reports and protocols
preparation of regulatory responses to health authorities
preparation of marketing authorisation applications (eCTD module 2)
simultaneously manage several projects and meet tight deadlines

What we offer

salary package to define according to skills and experience

Fulltime

Medical Writer

The healthcare industry requires that we abide by regulations from all around th...

Location

Malta , Marsa

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

BS or MS in scientific or clinical discipline with excellent writing skills
2 years of on-the-job experience in scientific/medical writing (e.g., clinical trial and regulatory documents) preferred but not mandatory
Knowledge of computer software Microsoft Word and Adobe Acrobat products
Microsoft Project and Visio are a plus
Experience in scientific and/or medical writing
Experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
Strong organizational skills and meticulous attention to detail
Familiarity with clinical trial-related and regulatory clinical submission templates and documents
Apply global regulatory authority regulations and/or guidance
Manage multiple projects with competing priorities

Job Responsibility

Develops high quality clinical documents ensuring scientific excellence and regulatory compliance
Writing, interpreting and summarizing clinical and non-clinical data
Compiling information and ensuring delivery within timelines
Ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
Collaborate with cross-functional team members and serve as MW representative at study team meetings
Prepare document timelines, with guidance from manager
Develop knowledge of one or more Baxter therapeutic areas

Medical Writer

We are currently looking for a Medical Writer or Senior Medical Writer to be at ...

Location

United Kingdom , Manchester / Macclesfield / London

Salary:

Not provided

Bioscript Group

Expiration Date

Until further notice

Requirements

Minimum 15 months medical writing experience in an MedComms agency
Evident writing skills and a passion for communicating complex ideas backed up with strong customer focus
Meticulous attention to detail and the ability to distil complex information for diverse audiences
A proactive approach to learning and staying informed about industry trends
Enthusiasm for working in a collaborative and dynamic environment

Job Responsibility

Translating complex scientific data into clear, concise, and accessible content
Collaborating with cross-functional teams to create compelling narratives to push the boundaries of medical science
Ensuring adherence to industry guidelines and regulatory standards
Conducting thorough research to stay abreast of the latest medical advancements
Developing educational materials and promotional content that help to bring the next generation of medicines to patients around the world

What we offer

25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
Enhanced sick and compassionate leave
Enhanced maternity, paternity & adoption leave
Birthday charity donation to a charity of your choice
Bonus Day off to be spent giving back to the community
Life Insurance and Critical Illness cover
Private Medical (Vitality for UK based colleagues)
Health cash plan or wellbeing allowance
International Employee Assistance Program

Medical Writer

We are looking for individuals to write and edit clinical documents to support r...

Location

Malta , Marsa

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

BS or MS in scientific or clinical discipline with excellent writing skills
2 years of on-the-job experience in scientific/medical writing preferred but not mandatory
knowledge of computer software Microsoft Word and Adobe Acrobat products
Microsoft Project and Visio are a plus
experience in scientific and/or medical writing
experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
strong organizational skills and meticulous attention to detail
familiarity with clinical trial-related and regulatory clinical submission templates and documents
apply global regulatory authority regulations and/or guidance
manage multiple projects with competing priorities

Job Responsibility

Develop high quality clinical documents ensuring scientific excellence and regulatory compliance
write, interpret and summarize clinical and non-clinical data
compile information and ensure delivery within timelines
ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
collaborate with cross functional team members and serve as MW representative at study team meetings
prepare document timelines, with guidance from manager, as needed
develop knowledge of one or more Baxter therapeutic areas.

Quality Assurance Specialist, Medical Communications

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experienced Medical Writer (1-2 years)
Scientific background and degree (PharmD, MD, PhD or Masters)
Knowledge of IT and digital solutions
Strong attention to detail and accuracy
Ability to manage and prioritize multiple, detailed activities
Results-orientated with fast and focused execution
Good communication, coordination and time management skills
Ability to work within a team or across multiple teams (including remotely) as well as independently
Fluent in oral and written English with high level of communication skills
Values teamwork, collaboration, and innovation

Job Responsibility

Cross check scientific information against cited references and ensure medical accuracy (fact check)
Ensure consistency with product label where applicable
Verify presence of essential information
Correct interpretation of scientific data from reference/sources
Alignment/formatting of content as per style guides/journal guidelines/congress guidelines
Ensure consistency of scientific content across different sections (including text, figures, tables)
Accurate bibliography/in-text citation and alignment of figures/graphs as per branding guidelines
Confirm that every sentence is source annotated, and each source annotation matches with respective reference and vice versa
Ensure that information is presented in a neutral manner without any interpretations and/or author’s conclusion
Track work and communicate with client team on job reviews, prioritization etc., through emails and teleconferencing if needed