Medical Writer Salary at Vedic Lifesciences BETA

How much does a Vedic Lifesciences Medical Writer make?

As of December 2024, the average annual salary for a Medical Writer at Vedic Lifesciences is $80,920, which translates to approximately $39 per hour. Salaries for Medical Writer at Vedic Lifesciences typically range from $72,050 to $88,372, reflecting the diverse roles within the company.

It's essential to understand that salaries can vary significantly based on factors such as geographic location, departmental budget, and individual qualifications. Key determinants include years of experience, specific skill sets, educational background, and relevant certifications. For a more tailored salary estimate, consider these variables when evaluating compensation for this role.

DISCLAIMER: The salary range presented here is an estimation that has been derived from our proprietary algorithm. It should be noted that this range does not originate from the company's factual payroll records or survey data.

Vedic Lifesciences Overview

Website:
vediclifesciences.com
Size:
<25 Employees
Revenue:
<$5M
Industry:
Pharmaceuticals

Vedic Lifesciences has been helping dietary ingredient and supplement companies with clinical trials, preclinical and toxicity studies (for GRAS and New Dietary Ingredient notifications) since 2000. The Vedic team remains at the leading edge of claims trends, outcome measures, and assessment tools applicable to dietary supplement research. Their claim substantiation studies have been used successfully in all major regions globally. Vedic Lifesciences remains one of the global leaders in nutrition industry research in terms of speed, credibility, and affordability.

See similar companies related to Vedic Lifesciences

What Skills Does a person Need at Vedic Lifesciences?

At Vedic Lifesciences, specify the abilities and skills that a person needs in order to carry out the specified job duties. Each competency has five to ten behavioral assertions that can be observed, each with a corresponding performance level (from one to five) that is required for a particular job.

  1. Medical Writing: A medical writer, working with doctors, scientists, and other subject matter experts, creates documents that effectively and clearly describe research results, product use, and other medical information. The medical writers also ensure that their documents comply with regulatory, journal, or other guidelines in terms of content, format, and structure. Medical writing as a function became established in the pharmaceutical industry because the industry recognized that it requires special skill to produce well-structured documents that present information clearly and concisely. All new drugs go through the increasingly complex process of clinical trials and regulatory procedures that lead to market approval. This demand for the clear articulation of medical science, drives the demand for well written, standards-compliant documents that medical professionals can easily and quickly read and understand. Similarly, medical institutions engage in translational research, and some medical writers have experience offering writing support to the principal investigators for grant applications and specialized publications.
  2. Clinical Research: Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical research is different from clinical practice. In clinical practice established treatments are used, while in clinical research evidence is collected to establish a treatment.
  3. Attention to Detail: Executing and completing a task with a high level of accuracy.
  4. Medical Communications: Medical communications are designed to stimulate awareness, discussion and procurement of new medical devices, drugs and treatments. Aimed at healthcare practitioners, buyers and stakeholders, it is a key aspect of pharmaceutical marketing
  5. clinical trial: Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments.

Related Jobs

Harvest Technical Services, Inc.
San Rafael , CA

Job Description Job Description Hybrid: San Rafael, CA Duties: The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. Responsibilities: Drafts and edits documents used for submissions including CTDs and RtQs. Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms. Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.). Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and com


Sponsored
12/13/2024 12:00:00 AM
Ivory Systems
San Rafael , CA

The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and


Sponsored
12/12/2024 12:00:00 AM
Tucker Parker Smith Group (TPS Group)
San Rafael , CA

Medical Writer Location: San Rafael, CA. (Hybrid) 7 month assignment (Potential to extend) Pay Rate: $52/hr. On behalf of our client a pharmaceutical company specializing in the development of therapeutics for patients dealing with rare genetic life threatening diseases. The Contract Medical Writer applies advanced expertise in document preparation and project management to support the development, drafting, review, and finalization of clinical study documents. These documents are critical for regulatory submissions and publications, ensuring the accurate reporting of clinical study results. Main Responsibilities: Draft and edit documents for regulatory submissions, including Common Technical Documents (CTDs) and Responses to Questions (RtQs). Develop and refine documents used in clinical studies, such as protocols, protocol amendments, and informed consent forms. Prepare documents for reporting aggregate safety and efficacy data, including investigator brochures and periodic safety re


Sponsored
12/12/2024 12:00:00 AM
Planet Pharma
San Rafael , CA

The Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and practices


Sponsored
12/12/2024 12:00:00 AM
Compass Consulting
San Rafael , CA

The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. Responsibilities: Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and


Sponsored
12/12/2024 12:00:00 AM
TalentBurst, an Inc 5000 company
San Rafael , CA

Position: Medical Writer, Req#: 35551628 Location: San Rafael, CA (Remote or hybrid depending on the location of the candidate (1-2 days in office to align with company policy)). Duration: 6+ Months Contract Job Description: The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. Education and Experience: Bachelor’s or higher degree; scientific focus desirable. Evidence of medical writing career development desirable, eg, American or European Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association. At least 5 years of experience required Medical writer in the pharmaceutical industry Medical or scientific writing experience as a primary job responsibilit


Sponsored
12/12/2024 12:00:00 AM
RootStaff
San Rafael , CA

Job Title: Medical Writer Location: San Rafael, CA 94901 (Hybrid) Duration: 6 months assignment Hourly pay range: $55-$57/hr Responsibilities: Drafts and edits documents used for submissions including CTDs and RtQs. Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms. Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.). Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes. Adheres to departmental procedures and practices and technical and industry standards during all aspects of work. Works effectively with cross-functional groups within client. Other tasks as assigned. Skills: Fulfils one of


Sponsored
12/12/2024 12:00:00 AM
Third Rock Ventures
Redwood City , CA

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Revolution Medicines is seeking an individual with strong organizational and communication skills to support medical writers in the planning and completion of high-quality, submission-ready clinical research documents. This role is an individual contributor reporting to the Senior Director, Medical Writing. This position is responsible for coordinating Medical Writing activities in a fast-paced environment and communicat


Sponsored
12/11/2024 12:00:00 AM

Check more jobs information at Vedic Lifesciences

Job Title Average Vedic Lifesciences Salary Hourly Rate
2 Clinical Research Coordinator $75,023 $36
3 Global Business Development Manager $79,720 $38
4 Assistant Manager, Accounts $55,940 $27
5 Assistant Project Manager $123,439 $59
6 Associate Director, Clinical Development $188,063 $90
7 Manager - Clinical Operations $172,414 $83
8 Manager, Clinical Development $118,791 $57
9 Manager, Marketing $126,817 $61
10 Admin Manager $99,548 $48
11 Assistant Manager $108,833 $52
12 Business Development Manager $145,980 $70

Hourly Pay at Vedic Lifesciences

The average hourly pay at Vedic Lifesciences for a Medical Writer is $39 per hour. The location, department, and job description all have an impact on the typical compensation for Vedic Lifesciences positions. The pay range and total remuneration for the job title are shown in the table below. Vedic Lifesciences may pay a varying wage for a given position based on experience, talents, and education.
How accurate does $80,920 look to you?

FAQ about Salary and Jobs at Vedic Lifesciences

1. How much does Vedic Lifesciences pay per hour?
The average hourly pay is $39. The salary for each employee depends on several factors, including the level of experience, work performance, certifications and skills.
2. What is the highest salary at Vedic Lifesciences?
According to the data, the highest approximate salary is about $88,372 per year. Salaries are usually determined by comparing other employees’ salaries in similar positions in the same region and industry.
3. What is the lowest pay at Vedic Lifesciences?
According to the data, the lowest estimated salary is about $72,050 per year. Pay levels are mainly influenced by market forces, supply and demand, and social structures.
4. What steps can an employee take to increase their salary?
There are various ways to increase the wage. Level of education: An employee may receive a higher salary and get a promotion if they obtain advanced degrees. Experience in management: an employee with supervisory experience can increase the likelihood to earn more.