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Remote Science Editor information
See California salary details
$35K - $41.4K
4% of jobs
$41.4K - $47.9K
13% of jobs
$49.9K is the 25th percentile. Wages below this are outliers.
$47.9K - $54.3K
26% of jobs
The median wage is $56.9K / yr.
$54.3K - $60.7K
17% of jobs
$60.7K - $67.1K
13% of jobs
$68.7K is the 75th percentile. Wages above this are outliers.
$67.1K - $73.5K
9% of jobs
$73.5K - $79.9K
9% of jobs
$79.9K - $86.4K
3% of jobs
$86.4K - $92.8K
0% of jobs
$92.8K - $99.2K
2% of jobs
$99.2K - $105.6K
3% of jobs
$35K
$63.2K
$105.6K
How much do remote science editor jobs pay per year?
What Are Remote Jobs for a Science Editor?
As a remote science editor, you review and edit content prior to its publication in a scientific journal. In this role, you may provide proofreading services, evaluate each proposed topic, or determine whether or not content meets the publication standards of your journal. This job comes in two primary forms: academic and popular science. Popular science usually includes mass-media releases like news articles, while academic science involves peer review and maintaining the reputation for scientific integrity within your journal. Regardless of publication type, this job requires extensive familiarity with the scientific process and the ability to determine whether or not any given piece of content is scientifically valid. Remote editors typically work through email, though you may occasionally speak with content writers or other publishing employees by phone.
What are the key skills and qualifications needed to thrive as a Remote Science Editor, and why are they important?
How do Remote Science Editors typically collaborate with researchers and other editors to ensure accuracy and clarity in scientific publications?
What does a Remote Science Editor do?
What is the difference between Remote Science Editor vs Remote Scientific Writer?
| Aspect | Remote Science Editor | Remote Scientific Writer |
|---|---|---|
| Required credentials | Advanced degree in science or related field, editing certifications | Degree in science, writing experience, possibly certifications |
| Work environment | Editing teams, academic or publishing settings, remote | Writing teams, research organizations, remote |
| Employer usage | Academic publishers, research institutions, scientific journals | Research firms, science communication agencies, publishers |
| Search intent | Editing, reviewing, ensuring scientific accuracy | Creating original scientific content, articles, reports |
Remote Science Editors focus on reviewing and refining scientific content for accuracy and clarity, often working with published materials. Remote Scientific Writers create original scientific content, such as articles and reports. While both roles require scientific knowledge, editors emphasize editing skills, whereas writers focus on content creation.
Senior Clinical Data Manager, Clinical Data Science
Ionis PharmaceuticalsCarlsbad, CA • On-site, Remote
Full-time
Posted 18 days ago
Job description
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.
With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.
We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!
SENIOR CLINICAL DATA MANAGER
CLINICAL DATA SCIENCE
SUMMARY:
The Senior Clinical Data Manager is responsible for all aspects of clinical data management throughout study conduct. The Senior Clinical Data Manager executes on policies and procedures for gathering, analyzing, and reporting clinical data for clinical trials that are conducted in compliance with Good Clinical Practice (GCP) and regulatory requirements.
RESPONSIBILITIES:
- Acts as lead data manager within study team
- Performs/oversees database development and management (e.g., CRF Specifications, Edit Check Specifications, Programming Specifications and QC, User Acceptance Testing, open, clean and lock of databases)
- Support the adoption and implementation of Clinical Data Warehouse technology to enable streamlined CDM data review strategies
- Implement Risk Management Planning on clinical studies
- Authors, reviews and/or approves various study related documents and plans (e.g., Data Management Plans, Data Transfer Agreements, CRF Completion Guidelines, Manual Review Guidelines)
- Manages and performs ongoing data management activities including CRF review, query generation, receipt and reconciliation of external data, SAE reconciliation, data listing generation and production of CDM summary reports (e.g. metrics) within projected study timelines.
- Performs medical coding of data using MedDRA & WHODrug dictionaries
- Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical Practices (GCP)
- Evaluates issues, recommend and implement solutions mitigation strategies as required
- Assists or leads with vendor selection process for outsourced CDM activities
- Oversees, as necessary, multiple External Service Provider (ESPs), contractors, or direct reports engaged to perform data management and EDC activities
- Participates in governance of External Service Provider (ESPs) across studies
- Participates in training of new hires and/or junior team members
- Supports regulatory inspection activities
- Oversees external data providers (e.g., IRT, central and specialty labs, patient diaries)
- Presents at investigator’s meetings and other data management trainings for study
- Escalates study related issues and communicates as appropriate with management and other functions
- Represents Clinical Data Management at study team meetings and facilitates cross-functional activities (e.g. Clinical Data Listing Reviews, database lock activities)
- Proactively addresses operational issues and clinical data questions
- Provides updates on study timelines, vendor oversight and other study related activities
- Liaises with the document specialists to ensure data management files are filed appropriately
- Implements best practices and industry standards across all data management activities
- Assists and leads department initiatives, process improvements, and cross functional initiatives
- Performs other duties, as appropriate
- Travel is variable and estimated at 10-20% domestic and international
COMPETENCIES:
- Excellent analytical and problem-solving skills
- Excellent organizational and time-management skills with ability to multitask and prioritize
- Strong interpersonal and communication skills
- Ability to effectively develop and manage relationships with internal and external stakeholders
- Excellent attention to detail
- Flexible to changing priorities
- Strong and positive work ethic
REQUIREMENTS:
- Bachelor’s Degree (BA/BS) preferred
- Minimum of five (5) years of direct Clinical Data Management experience, including at least 2 years of Study Lead Data Manager responsibilities.
- Experience with Electronic Data Capture (EDC) systems
- Working knowledge of CDISC CDASH and CDISC SDTM standards/guidelines
- Experience/training in the following areas: Good Clinical Practices (i.e. GxP Regulations; ICH Guidelines; Good Quality Practices), 21 CFR Part 11 and Computer Security (Part 11, Electronic Records; Electronic Signatures-Scope and Application; 21 CFR 11 and Industry Guidance; Computerized Systems Used in Clinical Trials), HIPAA, Drug Development and Approval Process, Data Management Overview
- Proficiency in MS Office including Word, Excel, and PowerPoint required
- Medical coding experience preferred but not required
Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS003961
Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits
Full Benefits Link: https://www.ionis.com/careers/working-at-ionis/#:~:text=our%20employee%20spotlight-,Benefits,-Employees%20are%20rewarded
The pay scale for this position is $95,000 to $151,418
NO PHONE CALLS PLEASE. PRINCIPALS ONLY.
Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.
About Ionis Pharmaceuticals
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
Carlsbad, CA, US
Year founded
1989