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Remote Study Director Jobs in Kansas (NOW HIRING)

Veristat

$128K - $169K/yr

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... study designs and regulatory requirements that apply to Phase I-IV clinical trials are required.

New

Overstory

... remote sensing fundamentals ... This is a great opportunity for someone who is energized by open scientific questions with direct ...

BigHand

Strategic Account Manager

KS · On-site +1

Track, qualify and route leads sent from all sources including but not limited to direct mail ... Fully remote working * Growing business with a global presence and a true focus on work-life ...

Genentech

Global Head of Legal Spend Management

Bern, KS · On-site +1

$213K - $396K/yr

You hold a Bachelor's degree in Business Administration, Finance, Economics, Legal Studies, Data ... Please note that fully remote working is not an option for this role. Relocation benefits are not ...

New

Akuity

Head of Product Marketing Remote The Company Akuity is a Sunnyvale, CA-based business founded to ... Define what "customer proof" looks like at Akuity and build the systems (case studies, reference ...

Icon plc

Global Head, Planning & Resource Management - Remote US, UK, Ireland, Poland, Canada ICON is a ... Study Start-Up, Data Management, Biostatistics, Pharmacovigilance, Medical Affairs, and other ...

Ag

Static Stress Engineer (Contract)

Wichita, KS · On-site +1

$52.50 - $72/hr

... and direct support to our airline customers. If you're interested in designing, creating, and ... Assignments may include detail part sizing, layout maturation, trade study analysis, weight ...

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Remote Study Director information

What is a remote study director?

A Remote Study Director is a professional responsible for overseeing and managing research studies or clinical trials from a remote location, rather than being physically present at the research site. Their duties include designing study protocols, coordinating with research teams, monitoring study progress, ensuring regulatory compliance, and maintaining data quality. Remote Study Directors use digital tools to communicate, track milestones, and manage documentation, making it possible to lead studies efficiently without being on-site. This role is common in fields like clinical research, pharmaceuticals, and academic studies, especially as remote work becomes more prevalent.

What are the key skills and qualifications needed to thrive as a remote study director?

To thrive as a Remote Study Director, you need a background in life sciences or a related field, experience in research project management, and a thorough understanding of study protocols. Familiarity with project management software, data collection tools, and compliance systems such as Good Clinical Practice (GCP) is typically required. Strong organizational, communication, and leadership skills help manage virtual teams and ensure studies stay on track. These competencies are critical for coordinating complex research projects remotely and ensuring regulatory compliance and data integrity.

How does a remote study director effectively manage communication and collaboration with dispersed research teams?

As a Remote Study Director, maintaining clear and consistent communication is essential for coordinating research activities and ensuring project milestones are met. You'll typically use a combination of video conferencing, project management platforms, and shared digital documentation to facilitate regular updates and resolve issues in real time. Establishing structured check-ins and transparent reporting processes helps keep team members aligned and informed, while also allowing you to promptly address challenges such as time zone differences or varying team member availability. Building trust and fostering a collaborative virtual environment are key to achieving successful study outcomes.

What is the difference between Remote Study Director vs Remote Clinical Project Manager?

AspectRemote Study DirectorRemote Clinical Project Manager
CredentialsTypically requires advanced degrees in life sciences and industry-specific certificationsRequires project management certifications and relevant experience in clinical trials
Work EnvironmentLeads study teams, oversees study design, and ensures compliance remotelyManages clinical trial projects, coordinates teams, and monitors progress remotely
Industry UsageCommonly used in pharmaceutical, biotech, and CRO sectorsWidely used in clinical research organizations and pharmaceutical companies

The Remote Study Director focuses on overseeing entire clinical studies, ensuring scientific and regulatory compliance, while the Remote Clinical Project Manager manages project timelines, budgets, and team coordination. Both roles require industry experience and often work remotely within the clinical research industry, but their core responsibilities differ in scope and focus.

What are popular job titles related to Remote Study Director jobs in Kansas?

For Remote Study Director jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Remote Study Director jobs in Kansas look for?

The top searched job categories for Remote Study Director jobs in Kansas are:

What cities in Kansas are hiring for Remote Study Director jobs?

Cities in Kansas with the most Remote Study Director job openings:

Remote Study Director jobs near you

Director, Regulatory Affairs

Remote

Veristat
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees
Learn more about Veristatexternal

$128K - $169K/yr

Full-time

Medical, Retirement

Posted 3 days ago

New

Job description

Job Description:

Director, Regulatory Affairs

Director Regulatory Affairs, responsible for strategic and operational regulatory consulting for client companies. The Director RA will be client facing and will be responsible amongst others for:

  • Strategic Advice to clients, with focus on early development through to NDA/ BLA
  • Independent preparation of regulatory documentation such as US IND, NDA/BLA modules, ODD, Fast track / other designations, FDA advice requests.
  • Scientific Interaction with internal cross functional teams
  • Client facing & Agency point of contact: Interaction with clients and FDA, lead interactions with Health Authorities
  • Internal BD & marketing facing role
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 $195K-223K 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 in science, toxicology, pharmacology, engineering or related field; Advanced Scientific degree such as Master's degree, Ph.D. or Pharm.D. preferred, with applied training relevant to clinical trials.
  • 10 years of relevant experience working directly for a CRO/ Pharmaceutical Company, with a minimum 5 years of experience leading regulatory development projects.
  • Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
  • Excellent written and oral communication skills including grammatical and technical writing skills, and familiarity with moderately complex study designs and regulatory requirements that apply to Phase I-IV clinical trials are required.
  • In-depth knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies.
  • Demonstrated ability to lead by example with demonstrated skill for technical and supervisory leadership of staff.
  • Skilled in use of computer software, including Microsoft Word and Microsoft Excel, and ability to learn new applications.
  • Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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