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Scientific Reviewer Jobs (NOW HIRING)

Join to apply for the Medical Reviewer/Safety Reviewer role at Collabera Join to apply for the ... scientific information that is more complex and requires more data than is supplied in the package ...

... scientific discipline reviewers, reviews these data to determine if the data are sufficient to justify changes in the labeling. * * The Data Scientist compiles data to prepare special reports related ...

... review board How will you get here? Be a self-starter with a passion for the advancement of patient care through clinical education, scientific engagement and professional networking. The position ...

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... review board How will you get here? Be a self-starter with a passion for the advancement of patient care through clinical education, scientific engagement and professional networking. The position ...

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... review board How will you get here? Be a self-starter with a passion for the advancement of patient care through clinical education, scientific engagement and professional networking. The position ...

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... review board How will you get here? Be a self-starter with a passion for the advancement of patient care through clinical education, scientific engagement and professional networking. The position ...

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... review board How will you get here? Be a self-starter with a passion for the advancement of patient care through clinical education, scientific engagement and professional networking. The position ...

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Scientific Reviewer information

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$10

$29

$48

How much do scientific reviewer jobs pay per hour?

As of May 30, 2026, the average hourly pay for scientific reviewer in the United States is $29.88, according to ZipRecruiter salary data. Most workers in this role earn between $22.60 and $36.54 per hour, depending on experience, location, and employer.

What is a Scientific Reviewer job?

A Scientific Reviewer evaluates scientific data, research findings, and technical documents to ensure accuracy, validity, and compliance with regulations or standards. They often work in regulatory agencies, journals, or research organizations, assessing study methodologies, experimental results, and conclusions. Their role is critical in maintaining scientific integrity and ensuring that published or approved research meets established guidelines. Additionally, they may provide recommendations for improvements or further studies based on their evaluations.

What are the key skills and qualifications needed to thrive in the Scientific Reviewer position, and why are they important?

To thrive as a Scientific Reviewer, you need a robust background in scientific research, critical analysis, and attention to detail, usually supported by an advanced degree in a scientific discipline. Familiarity with manuscript management systems, statistical analysis software, and databases like PubMed or Web of Science is common. Excellent communication, impartiality, and time management skills help set top Scientific Reviewers apart. These capabilities ensure thorough, objective evaluation of scientific work and timely collaboration within the review process.

What are some typical daily responsibilities of a Scientific Reviewer?

On a typical day, a Scientific Reviewer evaluates submitted scientific manuscripts, grant proposals, or research protocols for validity, originality, and adherence to ethical standards. They often collaborate with editors, fellow reviewers, and sometimes authors to provide constructive feedback and recommend acceptance, revision, or rejection of submissions. Responsibilities might also include checking data accuracy, reviewing statistical methodologies, and keeping up with current developments in one’s field. This role requires balancing rigorous analysis with clear written communication to support the advancement of quality research.
What cities are hiring for Scientific Reviewer jobs? Cities with the most Scientific Reviewer job openings:
What are the most commonly searched types of Scientific Reviewer jobs? The most popular types of Scientific Reviewer jobs are:
What states have the most Scientific Reviewer jobs? States with the most job openings for Scientific Reviewer jobs include:
Senior Scientific Manager - Parkinson's Disease

Senior Scientific Manager - Parkinson's Disease

AbbVie

Mettawa, IL

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


AbbVie rating

8.8

Company rating: 8.8 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

11th of 70 rated pharmaceutical


Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Provides support for assigned products within therapeutic area and is responsible for performing the accurate and detailed scientific review of medical content for promotional and non-promotional materials. Contributes to the creation of medical affairs externally facing and training materials in accordance with established polices and standards, including regulatory guidelines to meet customer needs. Functions in a scientific support role within assigned TA supporting on-market products. Acquires and establishes current therapeutic expertise necessary to serve as scientific, medical, and clinical to field medical teams/affiliates, TA teams, brand teams and R&D partners.

Responsibilities

List up to 10 main responsibilities for the job. Include information about the accountability and scope.

  • Identifies Insight Trends: Aids in the broader teams ability to address educational scientific gaps identified through the gathering of feedback from multiple field sources, compile and summarize to provide relevant insights.
  • Development of non-promotional field/affiliate resources: Develops non-promotional field/affiliate resources and ensures communications are supported by medical communication standards, pharmacovigilance standards, SOP's and all other quality and compliance standards in Medical Affairs.
  • Provides input into externally facing materials for use as directed : (i.e. Congress Booth, Ad Boards, Med Ed) with HCP or EE interactions (Payer, Patients, Prescribers, and Providers); educational initiatives (medical education, data, guidelines, and value proposition)
  • As directed, identifies, designs and implements focused and impactful internal training programs aiming to shape scientific understanding and medical practice (e.g. for Sales Representatives, MSLs, MOSLs, Affiliates)
  • Promotional Material Review: Responsible for performing the accurate and detailed medical review of advertising and promotional materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.
  • Evaluate literature, interpret data, write effectively, articulate information to a variety of internal and external audiences and effectively negotiate with counterparts from cross-divisional functional areas
  • Maintain understanding of product knowledge and labeling, associated disease states, relevant literature, treatment guidelines, competitor information
  • Evaluate risk and elevate as appropriate within the therapeutic area to ensure materials are compliant with applicable regulatory standards across all communication channels.
Qualifications
  • Scientific degree; advanced degree (e.g., MS, PhD, MD/DO, PharmD, NP, MSN) preferred.
  • 2-3 years of clinical, scientific/research, or industry related experience or equivalent required demonstrating strong leadership competencies and proven team-building skills with ability to lead in a global matrixed environment. Understanding of relevant therapeutic area required.
  • Basic knowledge of clinical trial design, results and methodology, regulatory and compliance requirements governing development of promotional and non-promotional materials is desirable.
  • Demonstrated analytical, conceptual and administrative skills. Excellent communication skills (written and presentation).
  • Flexibility and adaptability to organizational change and business priorities. Ability to work in a fast-paced corporate environment. High sense of urgency and commitment to excellence in the successful achievement of objectives.
  • Excellent planning and organizational skills. Ability to manage multiple priorities and demonstrate good business judgment.
  • Strong Project Management and Teamwork skills to address project risks and issues.
  • Ability to influence without direct authority to effectively deliver cross-functional projects
Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. 

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

  • This job is eligible to participate in our long-term incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html


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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013