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Writer jobs in Germany

Principal Medical Writer, Publications - Sponsor Dedicated - Immunology Experience (Home-based, US o

Principal Medical Writer, Publications - Sponsor Dedicated - Immunology Experience (Home-based, US o
Syneos Health Careers
Farnborough
USD 95,000 - 176,000
Urgently required
7 days ago
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Content Writer (Working Smarter with AI)

Content Writer (Working Smarter with AI)
Corndel.
London
GBP 35,000 - 50,000
Urgently required
7 days ago

Senior Writer, Science Frontiers - WIRED

Senior Writer, Science Frontiers - WIRED
CONDE NAST
London
GBP 30,000 - 50,000
Urgently required
7 days ago

GMP Data Reviewer & Technical Writer

GMP Data Reviewer & Technical Writer
ZipRecruiter
England
GBP 40,000 - 65,000
Urgently required
7 days ago

Technical Author

Technical Author
Blatchford
Basingstoke
GBP 40,000 - 50,000
Urgently required
3 days ago
Discover more opportunities than anywhere else.
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iGCSE English Language - Content Author

iGCSE English Language - Content Author
Medirest Signature
London
GBP 30,000 - 40,000
Urgently required
4 days ago

Scientific Editor: Cell Reports Medicine and the Research Integrity and Author Experience team

Scientific Editor: Cell Reports Medicine and the Research Integrity and Author Experience team
RELX INC
London
GBP 60,000 - 80,000
Urgently required
5 days ago

Technical Author

Technical Author
Adecco
Crewe
GBP 60,000 - 80,000
Urgently required
6 days ago
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Technical Author

Technical Author
PWHytek Ltd
Warrington
GBP 45,000 - 60,000
Urgently required
6 days ago

Technical Author - Adobe Indesign - F56377

Technical Author - Adobe Indesign - F56377
Caresoft Global Limited
Basildon
GBP 60,000 - 80,000
Urgently required
6 days ago

Technical Author

Technical Author
Akkodis
Stevenage
GBP 35,000 - 50,000
Urgently required
7 days ago

Associate Technical Author/ Copywriter

Associate Technical Author/ Copywriter
One Retail Group
London
GBP 28,000 - 35,000
Urgently required
7 days ago

Tester- Polaris Product Writer

Tester- Polaris Product Writer
Lorien
City Of London
GBP 45,000 - 65,000

Senior Bid Writer

Senior Bid Writer
Bid Solutions
London
GBP 45,000 - 60,000

Senior Bid Writer - Commercial Officer

Senior Bid Writer - Commercial Officer
Vector Recruitment
Cambridgeshire and Peterborough
GBP 45,000 - 53,000

Senior Bid Writer - Commercial Officer

Senior Bid Writer - Commercial Officer
Vector Recruitment
Bedford
GBP 45,000 - 53,000

Senior Writer, Science Frontiers - WIRED

Senior Writer, Science Frontiers - WIRED
Conde Nast
London
GBP 40,000 - 60,000

Principal Medical Writer

Principal Medical Writer
Ogilvy Health UK
London
GBP 45,000 - 65,000

Researcher / Writer

Researcher / Writer
Electrify Video Partners
United Kingdom
Remote
GBP 30,000 - 45,000

Senior/Principal Medical Writer

Senior/Principal Medical Writer
ICON Strategic Solutions
United Kingdom
Remote
GBP 50,000 - 75,000

Senior/Principal Medical Writer

Senior/Principal Medical Writer
ICON plc
United Kingdom
Remote
GBP 50,000 - 70,000

Technical Writer

Technical Writer
AeroCloud
St Albans
GBP 30,000 - 45,000

Associate Bid Writer

Associate Bid Writer
Serco Limited
London
GBP 30,000 - 40,000

Bid Writer

Bid Writer
Rockfield Specialist Recruitment
Ross-on-Wye
GBP 30,000 - 45,000

Technical Writer

Technical Writer
ZipRecruiter
Manchester
GBP 30,000 - 50,000

Principal Medical Writer, Publications - Sponsor Dedicated - Immunology Experience (Home-based, US o

Be among the first applicants.
Syneos Health Careers
Farnborough
USD 95,000 - 176,000
Be among the first applicants.
7 days ago
Job description
Description
Principal Medical Writer, Publications - Sponsor Dedicated - Immunology Experience (Home-based, US or Canada)

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.
Job Responsibilities

• Mentors and leads less experienced medical writers on complex projects, as necessary.

• Represents the Medical Writing department on clinical study teams, at conferences, meetings and for presentations to the client regarding a writing project.

• Advises clients and study teams on data presentation and production strategies and on data to ensure that client objectives/expectations are met and quality standards are maintained.

• Develops good working relationships with internal and external colleagues.

• Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.

• Develops or supports a variety of documents that include but not limited to: o Clinical study protocols and clinical protocol amendments; o Clinical study reports; o Patient narratives; o Clinical development plans; o IND submissions and annual reports; o Integrated summary reports; o NDA and (e)CTD submissions; o Investigator brochures, as well as; o Clinical journal manuscripts, clinical journal abstracts, and client presentations.

• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.

• Serves as peer reviewer providing review comments to give maximum clarity of meaning, accuracy relevance and to ensure that client objectives are met and overall quality standards are maintained.

• Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as company SOPs, client standards, and company and/or client approved templates when completing medical writing projects, on-time and on-budget.

• Performs on-line clinical literature searches, as applicable.

• Continues professional development to keep pace with regulatory guidance and client expectations that affect medical writing and to improve skills.

• Understands budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.

• Completes required administrated tasks within the specified timeframes.

• Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).

Qualifications

• Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.

• Extensive knowledge of English grammar with a familiarity with AMA style guide.

• Understanding of FDA and ICH regulations and guidelines strongly preferred.

• Demonstrated effective presentation, proofreading, and interpersonal, skills and ensure a team-oriented approach.

• Strong proficiency in Word, Excel, PowerPoint, email, and Internet.

• Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:
$95,000.00 - $175,700.00

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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