medical writer

CLIRNet

<div><div>Job Title: Medical Writer
</div><div>Location: Saltlake Sec V, Kolkata
</div><div>Mode: Work from Office</div><div></div><div>
Key Responsibilities:</div><div>
1. Curation of Scien tific Articles in Q&amp;A format based on new Medical research</div><div>
2. Editing MedWikis based on conversations between Doctors on newer Medical Research across specialties</div><div>
3. Edit the conversation scientifically (consult NCBI/Google scholar journals or Guidelines for clarification) using passive voice</div><div>
4. The content of an answer needs to be tallied with a Reputed Scientific article; any discrepancy needs to be checked and corrected accordingly (consult NCBI/Google scholar journals or Guidelines for clarification).</div><div>
5. The dose of any drug, any combination of drugs, or the duration of any therapy should be according to the International/ National Guidelines.</div><div>
6. Only the generic names of the drugs/devices should be used.</div><div>
7. The content prepared should be plagiarism free (less than 5% plagiarism is accepted).</div><div>
8. Suggestion of medically relevant topics of discussion for doctors as per the latest trends.</div><div></div><div>
Essential Skillset:</div><div>
1. Ability to write/edit Scientific content based on new Medical research</div><div>
2. Plagiarism-free writing</div><div>
3. Error-free writing style</div><div>
4. Excellent primary research skills</div><div>
5. Team Player</div><div>
6. Very strong outlook towards science/healthcare/life-science</div><div></div><div>
Education Qualification &amp; Experience:</div><div>
1. PHD Any branch of Life-sciences</div><div>
2. Freshers may also apply.</div></div>

Medical Writer

University of Kansas Medical Center

<div><div>Medical Writer - Cardiology</div> 

Department: 
SOM KC Cardiovascular Medicine 
- 
Translational Research 
 
Position Title: 
Medical Writer - Cardiology 
 
Job Family Group:
 
Professional Staff 
 
Job Description Summary: 
The Medical Writer will provide medical writing support to select faculty and staff and assist with the development of ideas and clinical topics related to medicine research for grants, publications, and presentations. Tasks include retrieving and summarizing data and information from literature searches and research studies; assisting faculty with the preparation of grants, manuscripts, and all other scientific presentation materials (e.g., presentations, posters, abstracts); as well as the development and implementation of scientific and grant writing training for faculty, residents and staff. 
 
Job Description: 
 
Job Responsibilities 
<ul><li>
Assist faculty &amp; staff with the preparation of grants, book chapters, manuscripts, and all other scientific presentation materials (e.g., presentations, posters, abstracts). 
</li><li>
Fact-check, clarify text, and prepare figures, such as tables, charts, legends, slides, and posters. 
</li><li>
Provide consultation services on research strategies, tactics, and tools. 
</li><li>
Deliver scientific, medical, technical, and business research/reference services. 
</li><li>
Review books, journals, technical reports, and electronic media relevant to health care needs.</li></ul> 
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. 
 
Required Qualifications 
 
Work Experience: 
<ul><li>
Four years of writing experience in scientific or healthcare area involving publication, grant, or clinical trial writing. Relevant education may substitute on a year for year basis.</li></ul> 

Preferred Qualifications 
 
Education: Master's or Ph.D. in Journalism, English, Communications, or Life Sciences. 
 
Work Experience: 
<ul><li>
Five years of writing experience in scientific or healthcare area involving publication, grant, or clinical trial writing. 
</li><li>
Experience with medical terminology. 
</li><li>
Experience with literature research.</li></ul> 

Skills 
<ul><li>
Communication. 
</li><li>
Analytical thinking. 
</li><li>
Critical thinking. 
</li><li>
Organization. 
</li><li>
Time management. 
</li><li>
Interpersonal skills. 
</li><li>
Attention to detail. 
</li><li>
Computer skills.</li></ul> 

Required Documents 
<ul><li>
Resume 
</li><li>
Cover Letter</li></ul> 

Comprehensive Benefits Package: 
 
Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html 
 
Employee Type:
 
Regular 
 
Time Type:
 
Full time 
 
Rate Type:
 
Salary 
 
Compensation Statement: 
 
The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
 
 
Pay Range: 
$60,800.00 - $91,200.00 
Minimum 
$60,800.00 
Midpoint 
$76,000.00 
Maximum 
$91,200.00 
 
Application Instructions: 
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Medical-Writer-Cardiology_JR009619 or go to https://careers.kumc.edu/ and search for position number JR009619. 
 
Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered. 
 
About KU Medical Center: 
The University of Kansas Medical Centers mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu. 
 
Benefits: 
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html 
 
Equal Employment Opportunity Statement 
 
The University of Kansas Medical Center is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ethnicity, ancestry, age, protected veteran or disability status, marital status, parental status, or genetic information. http://policy.ku.edu/IOA/nondiscrimination 
 
jeid-5994fcdd32129f4c859102fb80bd92d3</div>

Medical Writer - Cardiology

<div><h2 class="jobSectionHeader">Department:
</h2>SOM KC Cardiovascular Medicine
-
Translational Research
<h2 class="jobSectionHeader">Position Title:
</h2>Medical Writer - Cardiology
<h2 class="jobSectionHeader">Job Family Group:
</h2>Professional Staff
<h2 class="jobSectionHeader">Job Description Summary:
</h2>The Medical Writer will provide medical writing support to select faculty and staff and assist with the development of ideas and clinical topics related to medicine research for grants, publications, and presentations. Tasks include retrieving and summarizing data and information from literature searches and research studies; assisting faculty with the preparation of grants, manuscripts, and all other scientific presentation materials (e.g., presentations, posters, abstracts); as well as the development and implementation of scientific and grant writing training for faculty, residents and staff.
<h2 class="jobSectionHeader">Job Description:
</h2>Job Responsibilities
<ul><li>Assist faculty &amp; staff with the preparation of grants, book chapters, manuscripts, and all other scientific presentation materials (e.g., presentations, posters, abstracts).
</li><li>Fact-check, clarify text, and prepare figures, such as tables, charts, legends, slides, and posters.
</li><li>Provide consultation services on research strategies, tactics, and tools.
</li><li>Deliver scientific, medical, technical, and business research/reference services.
</li><li>Review books, journals, technical reports, and electronic media relevant to health care needs.
</li></ul>This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice.
Required Qualifications
Work Experience:
<ul><li>Four years of writing experience in scientific or healthcare area involving publication, grant, or clinical trial writing. Relevant education may substitute on a year for year basis.
</li></ul>Preferred Qualifications
Education: Master's or Ph.D. in Journalism, English, Communications, or Life Sciences.
Work Experience:
<ul><li>Five years of writing experience in scientific or healthcare area involving publication, grant, or clinical trial writing.
</li><li>Experience with medical terminology.
</li><li>Experience with literature research.
</li></ul>Skills
<ul><li>Communication.
</li><li>Analytical thinking.
</li><li>Critical thinking.
</li><li>Organization.
</li><li>Time management.
</li><li>Interpersonal skills.
</li><li>Attention to detail.
</li><li>Computer skills.
</li></ul>Required Documents
<ul><li>Resume
</li><li>Cover Letter
</li></ul>Comprehensive Benefits Package:
<div><div><div><div>Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html
</div></div></div></div><h2 class="jobSectionHeader">Employee Type:
</h2>Regular
<h2 class="jobSectionHeader">Time Type:
</h2>Full time
<h2 class="jobSectionHeader">Rate Type:
</h2>Salary
Compensation Statement:
The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
<h2 class="jobSectionHeader">Pay Range:
</h2>$60,800.00 - $91,200.00
Minimum
$60,800.00
Midpoint
$76,000.00
Maximum
$91,200.00</div>

Neural IT Pvt. Ltd.

Designation: Medical Writer Qualification: BHMS/BAMS Experience: 6 months to 4 yearsSkills Required:<ul><li>Sound knowledge of Pharmacology.</li><li>Proper understanding of various disease process, abnormal laboratory results, diagnosis and treatment.</li><li>Writing skills required.</li><li>Computer Skills.</li><li>Verbal and written communication in English.</li><li>Medical Summarization with thorough knowledge of medicine based on experience of working in hospital and its associate processes.</li></ul>Roles &amp; Responsibilities:<ul><li>Analyzing and understanding of medical reports with compilation into a document to create a medical review.</li><li>To draft a case in a chronological order that includes patient's history, disease process, assessment and intervention.</li><li>The job involves medical review by electronic adaptation of patient health records.</li><li>Proper channelizing of disease process.</li><li>Managing and Monitoring a team of Doctors.</li></ul>Job Types: Full-time, PermanentPay: ₹30,000.00 - ₹40,000.00 per monthBenefits:<ul><li>Health insurance</li><li>Provident Fund</li></ul>Application Question(s):<ul><li>How many years of experience you have in Medical drafting/writing?</li></ul>Work Location: In person

Non-Clinical, Medical writer

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Principal Medical Writer
At Thermo Fisher Scientific, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on &ndash; now and in the future.
Our Medical Writing team is growing, and we are looking for a Principal Medical Writer. This role is based in the United States.
Discover Impactful Work:
Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Regulatory Medical Writing documents, such as protocols, CSR, Investigator Brochures, and Marketing Applications, ensuring outstanding quality and compliance.
A Day in the Life:<ul><li>
Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.</li><li>
Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies. May research, write or edit complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.</li><li>
As an essential advisory member of the writing team, may provide training and mentorship for junior writers and program managers on document preparation, the use of software for document development strategy, document types, regulatory requirements, and industry best practices.</li><li>
May assist in program management activities. Identifies and resolves out-of-scope activities. Duties could include developing timelines, budgets, forecasts and contract modifications.</li></ul>
Keys to Success:<ul><li>
Acts with intensity</li><li>
Strong project management skills</li><li>
Excellent interpersonal skills including problem solving and negotiation</li><li>
Able to perform a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.</li></ul>
Education<ul><li>
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred</li></ul>
Experience<ul><li>
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).</li><li>
Experience in managing and directing complex Regulatory medical writing projects required</li><li>
Experience working in the pharmaceutical/CRO industry preferred</li><li>
Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.</li></ul>
Knowledge, Skills, Abilities<ul><li>
Significant knowledge of global, regional, national and other document development guidelines</li><li>
Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills</li><li>
In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, marketing application submissions, communications, etc</li><li>
Strong project management skills</li><li>
Excellent interpersonal skills including problem solving and decision-making</li><li>
Strong negotiation skills</li><li>
Excellent oral and written communication skills with strong presentation skills</li><li>
Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook); willingness to utilize technology to support authoring efficiency</li></ul>
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
What We Offer:
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We&rsquo;ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.</div>

Principal Medical Writer (Regulatory MW)

サイネオス・ヘルス

<div><div><div>Updated: Today 
Location: Pune, MH, India 
Job ID: 25104934
<div><div>Not ready to apply? 
Join our Talent Network
</div></div><div>Description
Senior Medical Writer (Medical Information Writing)
Syneos Health&reg; 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&rsquo;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<ul><li>
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.</li><li>
We are committed to our Total Self culture &ndash; 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.</li><li>
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 &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Mentors and leads less experienced medical writers on complex projects, as necessary.</li><li>
Acts as lead for assigned med info writing projects.</li><li>
Manages and coordinates medical information activities within and across departments with minimal supervision<ul><li>
Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers)
</li><li>Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide</li><li>
Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions
</li></ul></li><li>Experience in developing or supporting a variety of documents that include, but not limited to:</li><li>
Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.</li><li>
Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.</li><li>
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.</li><li>
Serves as peer reviewer on internal review team providing review comments on draft and final documents.</li><li>
Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.</li><li>
Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics.</li><li>
Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats)</li><li>
Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets.</li><li>
Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.</li><li>
Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.</li><li>
Completes required administrated tasks within the specified timeframes.</li><li>
Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).</li></ul>
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&rsquo;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.
Summary
Serves as a senior medical writer on clinical study or regulatory or publication project teams. Writes, edits, and coordinates content for clinical/regulatory/scientific while serving as primary technical contact with the internal team and the client.</div></div></div></div><div></div>

Senior Medical Writer (Medical Information Writing)

Syneos Health

<div>Description
Senior Medical Writer (Medical Information Writing)
Syneos Health&reg; 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&rsquo;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<ul><li>
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.</li><li>
We are committed to our Total Self culture &ndash; 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.</li><li>
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 &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Mentors and leads less experienced medical writers on complex projects, as necessary.</li><li>
Acts as lead for assigned med info writing projects.</li><li>
Manages and coordinates medical information activities within and across departments with minimal supervision<ul><li>
Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers)
</li><li>Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide</li><li>
Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions
</li></ul></li><li>Experience in developing or supporting a variety of documents that include, but not limited to:</li><li>
Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.</li><li>
Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.</li><li>
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.</li><li>
Serves as peer reviewer on internal review team providing review comments on draft and final documents.</li><li>
Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.</li><li>
Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics.</li><li>
Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats)</li><li>
Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets.</li><li>
Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.</li><li>
Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.</li><li>
Completes required administrated tasks within the specified timeframes.</li><li>
Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).</li></ul>
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&rsquo;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.
Summary
Serves as a senior medical writer on clinical study or regulatory or publication project teams. Writes, edits, and coordinates content for clinical/regulatory/scientific while serving as primary technical contact with the internal team and the client.</div>

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10000 medical writer jobs Near Me

Medical Writer

Medical Writer - Cardiology

Medical Writer - Cardiology

Non-Clinical, Medical writer

Principal Medical Writer (Regulatory MW)

Senior Medical Writer (Medical Information Writing)

Senior Medical Writer (Medical Information Writing)