senior medical writer

ProPharma Group

<div><div>For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.</div><div></div><div><div><div>
Essential Functions:</div></div></div><div><div><ul><li><div>
With minimal supervision, authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of clinical research and in various therapeutic areas including but not limited to: protocols, protocol amendments, study reports, patient narratives, IBs, ICFs, CEPs/CERs, DSURs, and plain language summaries, as well as more complex documents (e.g., PBRER, IND, NDA, BLA, MAA, eCTD submissionlevel documents).</div></li></ul></div><div><ul><li><div>
Supervises and mentors less experienced medical writers, as necessary.</div></li></ul></div><div><ul><li><div>
Adheres to established regulatory standards/guidelines including but not limited to: ICH E3/E6(R2), EU MDR/IVDR, Company standard operating procedures, client standards, and Company- and/or client-approved templates.</div></li></ul></div><div><ul><li><div>
Strives to complete medical writing deliverables on time and within budget.</div></li></ul></div><div><ul><li><div>
With minimal supervision, manages client expectations and interacts and communicates directly with clients, leads team meetings (e.g., project kickoff, comment review), and manages the deliverable timelines.</div></li></ul></div><div><ul><li><div>
Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce writing deliverables.</div></li></ul></div><div><ul><li><div>
Coordinates QC reviews of documents and maintains audit trails of changes as applicable.</div></li></ul></div><div><ul><li><div>
Reviews statistical analysis plans and table/figure/listing shells (as applicable) for appropriate content, grammar, format, and consistency.</div></li></ul></div><div><ul><li><div>
If requested by supervisor, performs QC review (e.g., reviews in-text tables against statistical output).</div></li></ul></div><div><ul><li><div>
Performs peer review of documents written by other medical writers, as required.</div></li></ul></div><div><ul><li><div>
Assists with project-related administrative tasks (e.g., creates and maintains timelines, updates deliverable trackers, hosts internal/client meetings).</div></li></ul></div><div><ul><li><div>
Maintains familiarity with current industry practices, regulatory requirements, and guidelines related to medical writing.</div></li></ul></div><div><ul><li><div>
Understands budget specifications for assigned deliverables, works within the budgeted hours, and communicates out-of-scope tasks to medical writing leadership.</div></li></ul></div><div><ul><li><div>
Supports multiple medical writing deliverables/projects simultaneously and manages own workload with minimal intervention from management team.</div></li></ul></div><div><ul><li><div>
Brings issues and potential concerns to line manager/client oversight manager&rsquo;s attention and proposes possible solutions for consideration by management team.</div></li></ul></div><div><ul><li><div>
Participates in departmental initiatives (e.g., process improvement, lunch and learns, etc.).</div></li></ul></div><div><ul><li><div>
Other duties as assigned.</div></li></ul></div></div><div></div><div><div><div>
Necessary Skills and Abilities:</div></div></div><div><div><ul><li><div>
Advanced knowledge of clinical research principles and demonstrated ability to interpret and present clinical data and other complex information.</div></li></ul></div><div><ul><li><div>
Advanced understanding of FDA (and other regulatory bodies as relevant to their role) and applicable regulations and guidelines.</div></li></ul></div><div><ul><li><div>
Advanced understanding of regulatory submission requirements and processes.</div></li></ul></div><div><ul><li><div>
Computer technology proficiency and expert word processing skills in MS Word, including required proficiency with tables, graphs, and figures.</div></li></ul></div><div><ul><li><div>
Exceptional project management skills and strong communication skills with a high attention to detail and quality.</div></li></ul></div><div><ul><li><div>
English language proficiency and familiarity with American Medical Association (AMA) style.</div></li></ul></div><div><ul><li><div>
Strong experience in relationship building and strategic collaboration on key business accounts.</div></li></ul></div><div><ul><li><div>
Thinks proactively, takes initiative, and willingly takes on new challenges.</div></li></ul></div><div><ul><li><div>
Ability to identify areas of concern or inefficiency and propose solutions for consideration by the management team to improve overall efficiency and quality of deliverables.</div></li></ul></div><div><ul><li><div>
Works independently with exceptional time-management skills and contacts management team proactively when additional support and resources are needed.</div></li></ul></div><div><ul><li><div>
Works effectively in a collaborative team environment.</div></li></ul></div><div><ul><li><div>
Demonstrates a growth mindset and positive outlook in all work activities.</div></li></ul></div></div><div></div><div><div><div>
Educational Requirements:</div></div></div><div><div><ul><li><div>
Bachelor&rsquo;s degree or higher, preferably in medical or scientific discipline.</div></li></ul></div></div><div></div><div><div><div>
Experience Requirements:</div></div></div><div><div><ul><li><div>
Minimum of 5 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics for a contract research organization, pharmaceutical company, or biotechnology company.</div></li></ul></div><div><ul><li><div>
Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a casebycase basis.</div></li></ul></div></div><div>
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.</div><div></div><div>
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.</div><div></div><div>
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.</div><div></div><div>
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***</div></div>

Senior Medical Writer

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
The Senior Medical Writer - Promotional Review, provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise and may provide assistance to the program manager.</p><p>
Additionally, as part of the Medical Affairs Consulting Team - the Senior Medical Writer may assist in medical affairs consulting services and the review of promotional medical materials against FDA-OPDP requirements. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.<br>
<br>
<b>What You'll Do:</b></p><p><i>
Medical Information</i></p><ul><li>
Serve as primary author who writes and provides input on routine medical information documents such as Standard Response Letters, Frequently Asked Questions (FAQs), and summarize data from clinical studies.</li><li>
Review routine documents prepared by junior team members. May provide training and mentorship for junior writers and program managers on document preparation, the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge.</li><li>
Ensure compliance with quality processes and requirements for assigned documents. Provide input on and independently develops best practices, methods and techniques for achieving optimal results, including various client specific processes.</li><li>
May assist in program management activities. Identify and resolve out-of-scope activities. Duties could include developing timelines, budgets, forecasts and contract modifications.</li><li>
Represent the department at project launch meetings, review meetings, and project team meetings.</li></ul><p><i>
Promotional Review and Medical Affairs Consulting</i></p><ul><li>
Reviews promotional and non-promotional materials for clinical and scientific accuracy against source documentation, reviews context and tone of language for compliance with applicable regulations and codes of practice (e.g., FDA, Health Canada, ABPI, EFPIA, IFPMA-AIFD) and assures appropriate level of language for intended audience (i.e., HCP, patient/consumer, other). Upon review and where consultative review comments are necessary, annotations are provided along with rationale and suggested language.</li><li>
Provide support for Medical Affairs and Field Force based materials, strategy planning, NCCN Submissions and other medical affairs-based activities.</li></ul><p><b><br>
Education &amp; Experience Requirements:</b></p><ul><li>
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred</li><li>
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).</li><li>
Equivalent of 3-years working experience in the independent review of promotional medical collateral as part of a Medical/Legal/Regulatory (MLR) Team or Promotional Review Committee</li><li>
Experience working in the pharmaceutical/CRO industry preferred</li><li>
Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous</li><li>
Strong background in Veeva PromoMats and related PRC CRM-based platforms.</li></ul><p><br>
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</p><p><b><br>
Knowledge, Skills, Abilities:</b></p><ul><li>
Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills</li><li>
Strong project management skills</li><li>
Excellent interpersonal skills including problem solving</li><li>
Strong negotiation skills</li><li>
Excellent oral and written communication skills with strong presentation skills</li><li>
Significant knowledge of global, regional, national and other relevant guidelines</li><li>
In-depth knowledge across therapeutic specialty areas.</li><li>
Great judgment and decision-making 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)</li></ul><p></p><p>
Join us as a Manager Operations &ndash; And lead our medical information operations team, oversee the development and dissemination of accurate medical and drug information, ensure compliance with regulatory standards, and support effective communication with healthcare professionals and stakeholders.<br>
<br>
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.<br>
<br>
<b>What You&rsquo;ll Do:</b></p><ul><li>
May supervise program staff providing medical/clinical information, utilizing medical/clinical background to participate in, manage, and conduct quality review of medical/clinical work.</li><li>
Oversee and/or complete development of client reports and procedural documents.</li><li>
Maintain thorough program knowledge, with an emphasis on medical/clinical content (where applicable), troubleshoot program issues, monitor and ensure compliance with company policies and procedures including SOP's, protocols, and other regulations by conducting quality monitoring of staff work.</li><li>
Act as liaison between the client, program management and staff for operational issues such as workflow processes, available resources</li><li>
Oversee all aspects of program training including conducting training, developing curriculum, and documenting and maintaining training records and</li><li>
curriculum</li><li>
Act as a resource for front line staff for assistance with managing their scope of service.</li><li>
May function as the front-line healthcare professional agent to cover services<br>
including but not limited to answering medical/clinical inquiries (where<br>
applicable) and documenting contacts, adverse events and product complaints.</li><li>
Manage staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations.</li><li>
Approve courses of action on salary administration, hiring, corrective action, and terminations. Review and approve time records, expense reports, requests for leave, and overtime.</li></ul><p></p><p><b>
Education and Experience:</b></p><ul><li>
Healthcare Degree (Bachelor's Degree in Pharmacy or Nursing. Or Associates Degree in Nursing with 2 years nursing experience)</li><li>
Previous experience (comparable to 5+ years) in the healthcare or pharmaceutical industry with responsibilities involving counseling or providing medical information to include leadership experience (comparable to at least 1 year).</li><li>
Education may be substituted in lieu of some years of experience for advanced degrees such as Pharm.D, Ph.D. or MS.</li><li>
In some cases a second language may be required.</li><li>
Some programs may require a Pharm.D.</li><li>
In most cases a license will be required.</li></ul><p><br>
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.<br>
<br>
<b>Knowledge, Skills, Abilities:</b></p><ul><li>
Manages experienced professionals and / or subordinate management who exercise latitude and independence in their assignments. Often heads one or more sections or a small department.</li><li>
Responsible for training and development of subordinate staff, estimating personnel needs, assigning work, meeting completion dates, assisting subordinates with difficult inquiries or problems, interpreting and ensuring consistent application of organizational policies, and development and implementation of unit policies and procedures</li><li>
Recommends employees for employment, discipline, termination; initiates and communicates a variety of personnel actions (e.g. performance and salary reviews, promotions, time off requests, timesheet and expense report approvals).</li><li>
Strong leadership skills</li><li>
Strong attention to detail and organizational skills</li><li>
Effective verbal and written communication skills</li><li>
Excellent problem solving and analytical skills</li><li>
Demonstrated time management skills and multi-tasking skills</li><li>
Strong interpersonal and decision-making skills</li><li>
Ability to coach and train staff</li><li>
Excellent language skills must be demonstrated if the position requires languages other than English</li><li>
Ability to work in a team environment and/or independently as needed</li></ul><p><b><br>
Work Environment:</b></p><p><i>
Thermo Fisher values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working </i><i>environment/requirements</i><i> for this role:</i></p><ul><li>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>
Able to work upright and stationary for typical working hours.</li><li>
Ability to use and learn standard office equipment and technology with proficiency.</li><li>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li><li>
May require travel. (Recruiter will provide more details.)</li></ul><p><br>
Why Join Us?<br>
<br>
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You&rsquo;ll work in an environment where collaboration and development are part of the everyday experience&mdash;and where your contributions truly make a difference.<br>
<br>
Apply today to help us deliver tomorrow&rsquo;s breakthroughs.</p><p></p><p><b>
Compensation and Benefits</b></p>
The salary range estimated for this position based in Massachusetts is $130,000.00&ndash;$150,000.00.<p></p><p>
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:</p><ul><li><p>
A choice of national medical and dental plans, and a national vision plan, including health incentive programs</p></li><li><p>
Employee assistance and family support programs, including commuter benefits and tuition reimbursement</p></li><li><p>
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</p></li><li><p>
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</p></li><li><p>
Employees&rsquo; Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</p></li></ul><p></p><p>
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards</p></div><p></p>

Senior Medical Writer, Promotional Review

Lehrer Family Chiropractic

<div><p>, remote</p><p>
We are seeking a talented and experienced Health Writer to join our team at Lehrer Family Chiropractic. As a remote employee, you will have the flexibility to work from the comfort of your own home while still making a meaningful impact on our practice.</p><p>
In this role, you will be responsible for creating engaging and informative health content for our website, social media channels, and other marketing materials. Your writing will play a crucial role in educating our patients and the general public about the benefits of chiropractic care and promoting our practice as a trusted source of health information.</p><p>
The ideal candidate will have a strong background in health writing, with a deep understanding of medical terminology and the ability to translate complex information into easy-to-understand content. You must also have excellent research skills and be able to fact-check your work to ensure accuracy.</p><p>
As a part-time remote employee, you will have the opportunity to work flexible hours that fit your schedule. This is a great opportunity for a self-motivated individual who thrives in a remote work environment and is passionate about health and wellness.</p><p>
Responsibilities:</p><ul><li>Write high-quality, engaging, and informative health content for our website, social media channels, and other marketing materials</li><li>Conduct thorough research on various health topics to ensure accuracy and credibility</li><li>Collaborate with our team to develop content ideas and strategies</li><li>Fact-check and proofread your work to ensure accuracy and consistency</li><li>Optimize content for SEO to improve our online visibility and reach a wider audience</li><li>Stay up-to-date with the latest health trends and developments to ensure our content is relevant and timely</li></ul><p>
Requirements:</p><ul><li>Bachelor's degree in journalism, communications, or a related field</li><li>Minimum of 2 years of experience in health writing</li><li>Excellent writing, editing, and proofreading skills</li><li>Strong research skills and ability to translate complex information into easy-to-understand content</li><li>Knowledge of SEO and experience in optimizing content for search engines</li><li>Ability to work independently and meet tight deadlines</li><li>Familiarity with chiropractic care and holistic health practices is a plus</li></ul><p>
We are excited to welcome a talented Health Writer to our team and help us spread the word about the benefits of chiropractic care. If you are a skilled writer with a passion for health and wellness, we encourage you to apply for this remote position.</p></div>

Remote Health Writer

Digilaxy Ltd

<p>We are seeking talented and detail-oriented individuals for the position of <b>Nursing / Medical Academic Writer</b> to join our team. The ideal candidate will possess strong nursing and medical knowledge, excellent academic writing skills, and a high level of proficiency in English. Prior experience in academic writing is highly preferred. BSN or MSN degree will be considered a strong asset.</p><p><b>Required Expertise:</b></p><ul><li>Nursing</li><li>Medical</li></ul><p><b>Key Responsibilities:</b></p><ul><li>Demonstrate strong reading comprehension and academic writing proficiency</li><li>Conduct high-quality, evidence-based academic research</li><li>Produce accurate, well-structured, original, and plagiarism-free content</li><li>Proofread and edit assignments to ensure clarity, accuracy, and adherence to guidelines</li><li>Adapt writing style to various academic formats and linguistic standards (e.g., APA, MLA, etc.)</li><li>Meet strict deadlines while maintaining high-quality standards</li><li>Maintain a professional, motivated, and positive attitude</li></ul><p><b>Qualifications:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Nursing (BSN/MSN) or a related medical field</li><li>Proven academic writing experience (preferred)</li><li>Strong research and analytical skills</li><li>Excellent command of written English</li><li>Ability to manage multiple tasks and work under tight deadlines</li></ul><p><b>Job Details:</b></p><ul><li><b>Work Type:</b> On-site</li><li><b>Job Type:</b> Full-time</li><li><b>Shift Availability:</b> Morning, Afternoon, Evening, and Night shifts available</li></ul><p>Pay: Rs35,000.00 - Rs65,000.00 per month</p><p>Work Location: In person</p>

Nursing/ Medical Writer (On-Site)

Astrik.Ltd

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
The Medical Writer will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.</p><p></p><p><b>
Job Responsibilities:</b></p><ul><li>
Develops and updates standard medical response documents, custom response documents, frequently<br>
asked questions, and Academy of Managed Care Pharmacy formulary dossiers, specific to the peri- and<br>
post-approval phases of the product lifecycle.</li><li>
Researches and responds to escalated medical information inquiries from healthcare providers.</li><li>
Conducts literature searches for standard response documents utilizing secondary databases.</li><li>
Utilizing professional judgment, integrates pertinent clinical data into standard response documents<br>
with clear, concise, accurate and balanced medical writing following organizational, client, and<br>
regulatory guidelines.</li><li>
Participates as required in project launch meetings, review meetings, and project team meetings, serving<br>
as a liaison for communication with the client.</li><li>
Collaborates and effectively communicates with internal and external client contacts to provide high<br>
quality medical information writing deliverables in a timely manner and within budget.</li></ul><p></p><div><p><b>
E</b><b>d</b><b>u</b><b>c</b><b>a</b><b>t</b><b>ion </b><b>a</b><b>n</b><b>d </b><b>E</b><b>x</b><b>p</b><b>e</b><b>r</b><b>i</b><b>e</b><b>n</b><b>c</b><b>e</b><b>:</b></p><ul><li><p>
PharmD</p></li><li><p>
Experience with Medical Information (equivalent to 2+ years)</p></li><li><p>
Previous experience that provides the knowledge, skills and abilities to perform the job (comparable to 2+ years)</p></li><li><p>
Experience working in the pharmaceutical/CRO industry preferred</p></li></ul></div><p></p><p><b>
K</b><b>n</b><b>o</b><b>w</b><b>l</b><b>e</b><b>dg</b><b>e</b><b>, </b><b>S</b><b>k</b><b>i</b><b>l</b><b>ls, </b><b>a</b><b>n</b><b>d </b><b>A</b><b>b</b><b>i</b><b>l</b><b>i</b><b>t</b><b>i</b><b>e</b><b>s</b><b>:</b></p><ul><li><p>
Solid medical writing skills, including grammatical, editorial and proofreading skills</p></li><li><p>
Ability to interpret and present complex data accurately and concisely</p></li><li><p>
Effective administrative, organizational and planning skills; attention to detail and quality</p></li><li><p>
Ability to work on own initiative and effectively within a team</p></li><li><p>
Effective oral and written communication skills
</p></li><li><p>Great judgment and decision-making skills</p></li><li><p>
Good computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)</p></li></ul><p></p><p><i>
Thermo Fisher values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:</i></p><ul><li>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>
Able to work upright and stationary for typical working hours.</li><li>
Ability to use and learn standard office equipment and technology with proficiency.</li><li>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li><li>
May require travel. (Recruiter will provide more details.)</li></ul></div><p></p>

Medical Writer - Medical Information

Increase Rev

<p>We&rsquo;re Hiring! | Content Writer &ndash; Increase Rev</p><p>We are looking for a creative and detail-oriented Content Writer to join our content team. The ideal candidate will assist in creating engaging, high-quality content for digital platforms while learning and growing under the guidance of senior writers and editors.</p><p>Key Responsibilities:</p><ul><li>Research industry-related topics (combining online sources, interviews and studies)&middot;</li><li>Produce organized draft with content management systems.</li><li>Before publishing, proofread and edit blog entries.</li><li>Work with the SEO team and follow SEO best practices to enhance site traffic.</li><li>Identify readers&rsquo; needs and gaps in our content and recommend new topics.</li><li>Ensure all-around consistency (style, fonts, images and tone) Update website content as needed.</li></ul><p>Requirements:</p><ul><li>Minimum Qualification Bachlor's or A-levels.</li><li>Minimum 1 year of experience as a Content Writer.</li><li>Experience doing research using multiple sources.</li><li>Excellent command of written English (grammar &amp; sentence structure).</li><li>Hands-on experience with Content Management Systems (e.g. WordPress) Ability to meet deadlines.</li></ul><p>Job Details:</p><p>Position: Content Writer<br/>Location: Gulshan-e-Iqbal, Karachi<br/>Type: On-site<br/>Salary: PKR 40,000 to 50,000<br/>Timings: 12 PM to 8 PM<br/>Working Days: Mon to Sat<br/>Job Types: Full-time</p><p>To Apply:</p><p>Send your CV at <b>jobs@increaserev.com</b></p><p>or WhatsApp at ‪‪+92 310 7263492‬‬</p><p>Mention &ldquo;Content Writer&rdquo; in the subject line.</p><p>Job Type: Full-time</p><p>Pay: Rs40,000.00 - Rs50,000.00 per month</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Work Location: In person</p>

Content Writer

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Senior Medical Writer

Senior Medical Writer, Promotional Review

Remote Health Writer

Nursing/ Medical Writer (On-Site)

Nursing/ Medical Writer (On-Site)

Medical Writer - Medical Information

Content Writer