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Medical Writer
$60k-77k (estimate)
Full Time
Just Posted
Hoskinson Health & Wellness Clinic is Hiring a Medical Writer Near Gillette, WY
The duty of a medical writer entails crafting clearly and concisely structured documents that effectively convey, scientific, clinical, educational and promotional information. The medical writer will possess a strong background in medical/technical writing, particularly in the context of clinical trials/research. This role requires a deep understanding of clinical research methodologies and regulatory requirements. AMedical writer will be responsible for producing well-structured documents presenting scientific, clinical, educational and promotional information clearly and concisely.
Regulatory & IRB Writing:
DISCLAIMER: Hoskinson Biotechnology, Hoskinson Health & Wellness Clinic, Hoskinson Construction, and all associated HBT entities are an equal opportunity employer. HBT does not discriminate in employment with regard to race, color, religion, national origin, citizenship status, ancestry, age, sex (including sexual harassment), sexual orientation, marital status, physical or mental disability, military status or unfavorable discharge from military service or any other characteristic protected by law.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for HBT to hire me. If I am hired, I understand that either HBT or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of HBT has the authority to make any assurance to the contrary.
I attest with my submission of this application that I have given to HBT true and complete information on this application. No requested information has been concealed. I authorize HBT to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
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Regulatory & IRB Writing:
- Create/write/maintain clinical trial protocols & reports, standard operating procedures (SOPs), and regulatory submissions
- Work closely with clinical research teams to gather and synthesize technical information, ensuring accuracy and compliance with regulatory standards (e.g., FDA, ICH-GCP, IRB)
- Develop and maintain informed consent forms, investigator's brochure, clinical overviews and summaries.
- Stay abreast of relevant regulations, guidelines, and industry standards governing clinical research, ensuring that all grant proposals and technical documents comply with applicable requirements
- Craft comprehensive investigator brochure that succinctly summarizes complex clinical trial data, ensuring accuracy, compliance, and clarity for regulatory submissions and investigator teams
- Adheres to department policies
- Create detailed trial/research budgets and financial narratives, accurately estimating project costs and its justifications
- Collaborate with internal (research teams) and external (IRB, CRO etc.) and other relevant teams to develop trial protocols, patents and reports
- Writing educational contents on health and medicine
- Promotional material for pharmaceutical and medical device products.
- Scientific articles intended for publications.
- Abstracts and posters designed for conferences
- Close relationship with a biostatistician
- Physical, sensory, and cognitive abilities sufficient to perform essential functions
- Strong analytical and financial skills for budgeting and financial narrative development
- Familiarity with government and foundation grant-making processes and requirements
- Strategic thinking and the ability to align grant opportunities with organizational needs
- Exceptional time management and organizational skills
- Ability to work independently and collaboratively in a team environment
- Good interpersonal and written and verbal communication skills
- A degree in life science preferably a masters/doctoral degree in medicine, biology or pharmacy.
- Minimum of 3-5 years of experience in medical writing and/or clinical research, with a focus on clinical trials
- Strong understanding of clinical research methodologies, including study design, patient recruitment, data collection, and analysis
- Proficiency in interpreting and applying regulatory requirements, such as FDA regulations, Good Clinical Practice (GCP) guidelines, and international standards
- Strong understanding of clinical trial/grant management and reporting
- Prolonged periods of sitting at a desk and working on a computer and standing, bending and moving
- Must be able to lift up to 15 pounds at times.
- If applicable, manage and mentor a team of technical writers and coordinators
- This is an onsite job opening*
- Health Insurance: Employer-sponsored health insurance, including a low-deductible health plan through Cigna, Vision, and Dental
- Additional Insurance: Employer monthly allotment for Disability, Life insurances, Cancer coverage, Accident policies, and more through a supplemental company
- Retirement: Highly matched 401(k)
- PTO & leave: Generous PTO and sick leave with accrual and carry-over opportunities
- Continuing or Additional Education: HH&WC will assist in the professional development of all employees with HR approval
DISCLAIMER: Hoskinson Biotechnology, Hoskinson Health & Wellness Clinic, Hoskinson Construction, and all associated HBT entities are an equal opportunity employer. HBT does not discriminate in employment with regard to race, color, religion, national origin, citizenship status, ancestry, age, sex (including sexual harassment), sexual orientation, marital status, physical or mental disability, military status or unfavorable discharge from military service or any other characteristic protected by law.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for HBT to hire me. If I am hired, I understand that either HBT or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of HBT has the authority to make any assurance to the contrary.
I attest with my submission of this application that I have given to HBT true and complete information on this application. No requested information has been concealed. I authorize HBT to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
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Job Summary
JOB TYPE
Full Time
SALARY
$60k-77k (estimate)
POST DATE
05/30/2024
EXPIRATION DATE
06/19/2024
Show more
The job skills required for Medical Writer include Medical Writing, Clinical Research, Medical Communications, Clinical Trial, Analysis, Verbal Communication, etc. Having related job skills and expertise will give you an advantage when applying to be a Medical Writer. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Medical Writer. Select any job title you are interested in and start to search job requirements.
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The following is the career advancement route for Medical Writer positions, which can be used as a reference in future career path planning. As a Medical Writer, it can be promoted into senior positions as a Medical Writer III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Medical Writer. You can explore the career advancement for a Medical Writer below and select your interested title to get hiring information.
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