Pharma English QC Specialist - Regulatory & Clinical Content
Welo Global
Welo Life Sciences, a Welo Global brand, seeks detail-obsessed QC specialists to join its non-Linguistic QC team. You will perform quality control of translations into English for pharmacovigilance, regulatory, and clinical content, ensuring accuracy in regulated documents. Ideal candidates have CAT tools experience, QA checks, and track changes proficiency, with 6 months in language QA. This role offers steady daily volume, flexible hours (4–5 per day), and opportunities to impact patient #J-18808-Ljbffr Welo Global
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Pharma English QC Specialist - Regulatory & Clinical Content in New York, NY vacancy
- ...take control of their content supply chain. Some reasons... ...working with over 50+ pharma brands.Frontiers of... ...for medical accuracy, clinical soundness, and... ...Looking ForDeep medical and regulatory expertise: Strong understanding... ...in Life Sciences or English.Excellent written and...ContentRegulatoryEnglish language skills
Solstice Health
New York, NY3 days ago - ...pharmaceutical and CRO clients. We are seeking detail-obsessed QC specialists who take pride in catching what others miss; your work will ensure accuracy in regulator-ready translations and clinical content. Join a high-visibility program with steady daily volume and long...ContentPart timeWeekend work
$85k - $95k
...Description Tris Pharma, Inc. ( is a leading privately... ...Quality Control (QC) and Analytical R&D (AR... ...related compounds analysis, content/blend uniformity, particle... ...projects Fluent in English (verbal and written) Ability... ..., cGMPs and SOPs regulatory rules, regulations and...ContentRegulatoryEnglish language skillsWork experience placementWork at officeLocal areaImmediate startTris Pharma
New York, NY3 days ago$128k - $176k
...SME contribution to develop content for regulatory submissions that is well‑... ...degree in a scientific or clinical discipline or related field... ...of related, sponsor‑level pharma or biotech clinical/regulatory... ...bilingual or fluent American English proficiency. Solution‑...ContentRegulatoryEnglish language skillsTemporary work$280k - $340k
Director, Clinical Development Lead, Hematologic Malignancies... ..., scientific, and regulatory requirements. Oversee... ...and report scientific content of protocols,... ...preferably 3+ years in biotech/pharma). Clinical trial... ...Excellent oral and written English communication skills,...ContentRegulatoryEnglish language skillsFull time$160.5k
...retains first-hand clinical insight that... ...quality in scientific content and interaction... ...Information team / specialists; affiliate... ...Public Affairs; Regulatory Affairs; Legal; OEC... ...scientific/research, or pharma industry related... ...language and English preferred). Proven...ContentRegulatoryEnglish language skillsLocal areaAbbVie
New York, NY3 days ago- Senior Director, Clinical Science - Hematology Responsibilities Provide... ...and present scientific content and cross-study insights. Provide... ...with Clinical Operations, Regulatory Affairs, Biostatistics/Data Management... ...oncology/related function (pharma/biotech). Deep expertise in...ContentRegulatory
$280k - $340k
...The Medical Director, Clinical Development Lead, Hematology... ...of compliance and regulatory requirements, Menarini... ...of scientific content of protocols, Investigator... ...experience in Biotech/Pharma industry. Clinical trial... ...oral and written English communication skills,...ContentRegulatoryEnglish language skillsWork at officeRemote work- ...for a New Challenge? Keep Your Clinical Skills Sharp—From Home! Are... ...compliance with client agreements, regulatory guidelines, and federal/state... .../or publications. Ensure the content, format, and professional... ...possess excellent skills in English usage, grammar, punctuation...ContentRegulatoryEnglish language skillsLocal areaRemote workWork from homeMonday to FridayNight shiftRotating shift
- Incident Response Specialist PH - Fully Remote The Incident Response... ...Support evidence collection for regulatory or legal requirements.... ...Support development of detection content. Assist with automation opportunities... ...or Incident Response. Strong English communication skills....ContentRegulatoryEnglish language skillsRemote work
$96.2k - $151.4k
...Specialist, Document SystemsSkip to main content*This site uses cookies to provide you with an optimal user experience... ...coordinate, assemble, and manage regulatory documents for internal studies... ...skills (including a strong command of English grammar, editing, and...ContentRegulatoryEnglish language skillsFor contractorsWork at officeLocal areaRelocationVisa sponsorshipFlexible hoursMSD Malaysia
New York, NY2 days ago- ...execution, and interpretation of clinical trials or research activities... ...knowledge of compliance and regulatory requirements, AbbVie’s... ...and reporting of scientific content of protocols, Investigator Brochures... ...excellent oral and written English communication skills. Applicable...ContentRegulatoryEnglish language skillsLocal area
- ...Director of PET and with the clinical supervision of the... ...in compliance with regulatory agencies and in accordance... ...to optimize information content as directed by reading... ...Must be able to perform QC on dose calibrators (... ...Languages: English Read Write Speak...ContentRegulatoryEnglish language skillsWork at officeFlexible hoursShift work
Compu-Vision Consulting
New York, NY4 days ago $200k - $240k
...We invest in and advance our own clinical‑stage programs, using our AI platform... ...integrity. Contribute to regulatory submissions Prepare scientific content for regulatory authority interactions... ...experience in biotech or pharma, with direct ownership of protocol...ContentRegulatoryWork at officeRemote work$238k - $280k
...patients. Advanced technology, a world‑class clinical development organization, and state‑of... ...in the preparations of the clinical content of regulatory submissions/documents (e. g. NDA, MAA,... ...to perform other duties, as assigned. #J-18808-Ljbffr Taiho Pharma Canada, Inc.ContentRegulatoryInterim roleLocal area- .../Physician in preparation of clinical/medical services. Working in... ...health environment (hospital, regulatory agency, or outpatient setting... ...to read, write and speak the English language. Major Responsibilities... ...or guidelines, including the contents of this job description, at...ContentRegulatoryEnglish language skillsFull timeWork experience placementMonday to Friday
$85 per hour
...adjustment recommendations for clinical accuracy, documentation support, and regulatory compliance Review medical records... ...Exceptional written and verbal English communication skills ~ High... ...risk adjustment and HCC coding content Experience presenting risk adjustment...ContentRegulatoryEnglish language skillsRemote jobHourly payWeekly payContract workPart timeFor contractorsFlexible hours$170k - $190k
Senior Manager, Global Regulatory Affairs Labeling This range is provided by Planet Pharma. Your actual pay will be based on your... ...consensus of proposed labeling content via the Labeling Working Group... ...., document management system, QC of the CCDS and other labeling...ContentRegulatoryFull timeWork experience placementLocal areaRemote work- Piper Companies is seeking a Cardiology Clinical Research Associate to support a growing clinical research program in cardiovascular... ...integrity, and support investigative sites in compliance with regulatory standards and study protocols. Candidates should have a life sciences...Regulatory
$67.63k
...health services. Ensure alignment with clinical best practices and organizational standards... ..., and field-informed insights. Ensure content is relevant, culturally responsive, and... ..., findings, and recommendations. Uphold regulatory requirements and organizational quality...ContentRegulatoryThe New York Foundling
New York, NY3 days ago- ...our localization team. You’ll review, localize, fact check, translate, and adapt football-related content so it resonates with audiences in your market. Language pair: English (US) → Ukrainian (Ukraine). Tasks include quality control, translation, copy-editing, MTPE, and...ContentEnglish language skillsRemote job
- ...to be recruiting an Advanced Clinical Pharmacist based at... ...plan, organise and deliver a specialist clinical pharmacy service within... ...PVG member for the required regulatory group (i.e. child and/or adult... ...Applications that rely on AI-generated content may be withdrawn. By...ContentRegulatory
- ...knowledge of current Good Manufacturing Practices (cGMP) and other regulatory requirements. More than 5 years of experience in... ...writing validation, commissioning, and technical documentation in English. Proficient in MS Office applications (Word, Excel,...RegulatoryEnglish language skillsRemote work
Mentor Technical Group
New York, NY1 day ago - ...are seeking a senior QA specialist who will play a... ...archiving in accordance with regulatory timelines Training... ..., including following QC processes, proper document... ...risk assessments for clinical projects, software... ...communicate effectively in English (spoken and written)...RegulatoryEnglish language skillsWork at officeRemote work
- BeOne is seeking a Start-up Specialist to manage country-specific... ...with the Regional Clinical Operations Manager to meet... ...standards, and support in regulatory submissions and essential... ...of start-up experience in pharma/CRO, fluent English and Dutch, and strong organizational...RegulatoryEnglish language skills
- ...capturing real patient moments and surgeon content that stops the scroll, builds trust, and... ...and front-desk staff so filming fits the clinic flow. Light community management —... ...What you bring — must-haves: Fluent English and Spanish — comfortable on camera and...ContentEnglish language skillsWork at officeLocal area
Goals Aesthetics & Plastic Surgery
New York, NY16 days ago - ...facilitating all phases of content development and quality control (QC) for a diverse portfolio... ...role involves preparing clinical presentations, expert... ...Networking with clinical specialists and medical/scientific... ...extensive knowledge of English grammar and AMA standard...ContentEnglish language skillsWorldwideFlexible hours
$96k - $150k
Join to apply for the Principal Regulatory Medical Writer role at Aquestive Therapeutics... ...to regulatory inquiries, and clinical study reports (CSRs). Additionally,... ...with strategy within and across content of documents. • Review and QC documents for consistency, scientific...ContentRegulatory16 hoursFull timeContract workLocal area- Job Description The Senior Director, Clinical Science - Hematology is responsible for providing... ...collaboration with Clinical Operations, Regulatory Affairs, Biostatistics and Data... ...preparation of clinical and scientific content for governance discussions, program reviews...ContentRegulatoryWork experience placement
- ...level titles such as Marketing Specialist, Marketing Campaign... ...and execution for the company Clinical Assessment across the Netherlands... ...must be fluent in Dutch and English (German would be a bonus!) and... ...leadership and clinical education content, and case studies/success...ContentEnglish language skillsFull timeFixed term contractLive inLocal areaRemote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Pharma English QC Specialist - Regulatory & Clinical Content. Be the first to apply!
Related searches
- loss prevention specialist New York, NY
- fixed income specialist New York, NY
- total rewards specialist New York, NY
- settlement specialist New York, NY
- inclusion specialist New York, NY
- accessibility specialist New York, NY
- hearing aid specialist New York, NY
- orientation and mobility specialist New York, NY
- skin specialist New York, NY
- health science specialist New York, NY