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Senior English Writing Jobs (NOW HIRING)

Gan & Lee Pharmaceuticals

Excellent written and oral communicator in English. * Strong proficiency in major Microsoft Office products (i.e., Word, Excel, PowerPoint, Project). * Enthusiastic, genuine, ethical, fair, and loyal ...

NBCUniversal

Sr. News Writer

Miami, FL · On-site

The Senior Noticiero Writer is responsible for writing and producing daily scripts for live ... Minimum 5 years of news writing experience * Must be fully fluent in English and Spanish (both ...

LSU AgCenter

Instructor - English

Allen, TX

... of Senior Instructor. We have a growing and exciting program that reflects a long-standing and committed community of writing faculty here at LSU in Baton Rouge. Required Qualifications: Master ...

Veristat

Minimum of 5 years of medical writing experience in a contract research organization or ... Excellent written English and keen attention to detail. * Strong interpersonal and communication ...

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As of Jul 14, 2026, the average yearly pay for senior english writing in the United States is $92,559.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,000.00 and $101,000.00 per year, depending on experience, location, and employer.
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Senior English Writing jobs near you
Infographic showing various Senior English Writing job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $92,559 per year, or $44.5 per hour.

Senior Manager, Clinical Scientist

Gan & Lee Pharmaceuticals

Remote

Full-time

Posted 21 days ago

Job description

SummaryThis position reports to the Head of Clinical Development at Gan & Lee Pharmaceuticals USA Corporation or designee. The position will work with Gan & Lee clinical program lead(s) to provide the scientific and clinical leadership and inputs in meeting the development objectives for the program.Education and Credentials
  • Medical Degree, PhD, or PharmD.
Experience
  • At least 2-4 years in clinical development experiences at a pharmaceutical, biotechnology, CRO company, clinical training/practice, and/or academia.
  • Experiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus.
  • Board eligibility or certification preferred
Skills
  • Demonstrated ability to manage multiple and diverse projects concurrently.
  • Demonstrated ability to develop positive relationships and collaborations.
  • Strong analytical skills; a strategic thinker, planner, and implementer.
  • Solid scientific skills and attentive to details.
  • Working knowledge of biostatistics is a plus.
  • Ability to operate independently with minimal supervision.
  • Deep experience with literature analysis, proven technical English writing skills.
  • Excellent written and oral communicator in English.
  • Strong proficiency in major Microsoft Office products (i.e., Word, Excel, PowerPoint, Project).
  • Enthusiastic, genuine, ethical, fair, and loyal to the organization and its vision and goals.
Responsibilities
  • Provides scientific and/or medical expertise for clinical research aspects of the project.
  • Participates in strategic meetings/advisory boards as key clinical research representative.
  • Provides medical and scientific input to the core documents for the project (e.g., product strategy documents, target product profile (TPP), protocols, submission, etc.).
  • Consults with internal/external stakeholders and internal/external key opinion leaders.
  • Provides support to other functional members of the project team.
  • Interacts with investigators and CROs as the medical or scientific representative.
  • Provides medical and scientific interpretation of efficacy and safety data.
  • Participates in the interactions with regulatory authorities (e.g., FDA, EMEA meetings). This includes developing key documents, participating in the preparation for meetings with the health authorities, and participating in the meetings and interactions with the health authorities. 
  • Provides input for a project publication plan, liaises with commercial and works on launch activities when required.
  • Creates and reviews abstracts, and manuscripts created by internal or external sources.

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