Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...
CRA II
Lawrence, KS · Remote
$91K - $114K/yr
Contributing to the preparation and review of study documentation, including protocols and clinical ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
CRA II
Lawrence, KS · Remote
$91K - $114K/yr
Contributing to the preparation and review of study documentation, including protocols and clinical ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
CRA II
Lawrence, KS · Remote
$91K - $114K/yr
Contributing to the preparation and review of study documentation, including protocols and clinical ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
Quick apply
CRA II
Lawrence, KS · Remote
$91K - $114K/yr
Contributing to the preparation and review of study documentation, including protocols and clinical ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
North America | Remote | Sponsor-Dedicated (FSP) Opportunities ICON is a global healthcare ... Identify and proactively resolve site and study issues * Collaborate with cross-functional teams to ...
North America | Remote | Sponsor-Dedicated (FSP) Opportunities ICON is a global healthcare ... Identify and proactively resolve site and study issues * Collaborate with cross-functional teams to ...
Imaging Specialist Manager
Wichita, KS · On-site +1
... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...
Imaging Specialist Manager
Wichita, KS · On-site +1
... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Quick apply
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Quick apply
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Quick apply
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Quick apply
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Act as the primary contact and study lead with the customer from startup through close-out of a ...
Through ongoing, clinically-led career resources and support, were meeting the needs and creating ... An extensive virtual library of peer-reviewed studies and online assessments, including online ...
Quick apply
Through ongoing, clinically-led career resources and support, were meeting the needs and creating ... An extensive virtual library of peer-reviewed studies and online assessments, including online ...
Provide coaching to junior staff for study level documents as well as submission level documents ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...
Provide coaching to junior staff for study level documents as well as submission level documents ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Clinical Research Associate II
Lenexa, KS · Remote
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Remote Clinical Study Startup information
What is a remote clinical study startup?
A Remote Clinical Study Startup refers to the initial phase of setting up clinical trials, conducted primarily through digital tools and remote processes. This includes activities like site identification, regulatory submissions, contract negotiations, and ethics approvals, all managed without requiring in-person meetings. Remote startups leverage technology to streamline processes, reduce timelines, and improve collaboration among stakeholders. This approach is especially useful for multi-site studies or when in-person interactions are limited by geography or global events.
What are the key skills and qualifications needed to thrive as a remote clinical study startup specialist?
To thrive as a Remote Clinical Study Startup Specialist, you need a solid understanding of clinical trial processes, regulatory requirements, and project management, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential. Strong organizational skills, attention to detail, and effective communication are vital soft skills for coordinating teams and ensuring timely study activation. These skills and qualities are crucial for maintaining compliance, minimizing delays, and driving successful clinical trial launches in a remote environment.
What are some common challenges faced in a remote clinical study startup role, and how can they be addressed?
Professionals in Remote Clinical Study Startup roles often encounter challenges such as coordinating documentation across multiple sites, ensuring regulatory compliance in different regions, and maintaining clear communication among dispersed teams. Successfully overcoming these hurdles typically involves leveraging robust digital tools for project management and document tracking, as well as establishing standardized communication protocols. Proactive problem-solving and strong organizational skills are essential for keeping timelines on track and ensuring all study startup activities are completed efficiently.
What is the difference between Remote Clinical Study Startup vs Remote Clinical Trial Coordinator?
| Aspect | Remote Clinical Study Startup | Remote Clinical Trial Coordinator |
|---|---|---|
| Primary Role | Planning and initiating clinical studies, including site selection and regulatory submissions | Managing daily trial activities, site communication, and data collection |
| Required Credentials | Typically a background in life sciences, clinical research certifications preferred | Similar credentials, often with clinical research or coordinator certifications |
| Work Environment | Primarily remote, collaborating with sponsors, CROs, and sites | Remote or hybrid, focusing on site management and data oversight |
| Industry Usage | Used during study initiation phase | Used during trial execution phase |
Remote Clinical Study Startup involves planning and launching new clinical trials, while Remote Clinical Trial Coordinator focuses on managing ongoing trial activities. Both roles require similar credentials and often operate remotely within the clinical research industry, but they differ in their specific responsibilities and timing within the study lifecycle.
What are the most commonly searched types of Clinical Study Startup jobs in Kansas?
The most popular types of Clinical Study Startup jobs in Kansas are:
What are popular job titles related to Remote Clinical Study Startup jobs in Kansas?
For Remote Clinical Study Startup jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Study Startup jobs in Kansas look for?
The top searched job categories for Remote Clinical Study Startup jobs in Kansas are:
What cities in Kansas are hiring for Remote Clinical Study Startup jobs?
Cities in Kansas with the most Remote Clinical Study Startup job openings:
Job description
Job Description:
Position overview
The Senior Medical Writer- Clinical Focus is a major contributor to document authorship for a variety of documents across different service lines. The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. Veristat is looking for individuals looking to use their expertise in clinical regulatory writing to lead teams and help clients achieve their goals.
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture - 70% remote workforce, 66% women-led teams
Learn more about our core valueshere!
What we offer
- The estimated hiring range for this role is $116K-128K plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
- Benefits vary by location and may include:
- Remote working
- Flexible time off
- Paid holidays
- Medical insurance
- Tuition reimbursement
- Retirement plans
What we look for
- Bachelor's degree or higher in a scientific discipline strongly preferred
- 3+ years of regulatory writing experience or equivalent experience with clinical related documentation
- Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance
- Experience in the development of submission-level documents (does not require functioning as a document lead)
- Experience in the development of clinical documents such as Clinical Study Reports, Investigator Brochures, protocols, ISS, and/or ISE
Skills & Abilities:
- Intermediate proficiency with Microsoft Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques
- Strong understanding of the document creation process and of the drug development lifecycle
- Able to synthesize data across multiple data sources and documents to create summary reports
- Ability to conduct/lead a CRM and successfully lead a project team to consensus
- Ability to use logical arguments to persuade others when presenting ideas and suggestions, but also respond positively to opposing views voiced by others
- Develops professional relationships with clients as a way to further the business relationship and maintain current industry knowledge
- Ability to identify and institutionalize work practices that are most effective in order to ensure consistency in performance
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
About Veristat
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Southborough, MA, US
Year founded
1994