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Remote Study Director Jobs (NOW HIRING)

Danaher

Senior Clinical Study Manager

... will be a remote role. In this role, you will have the opportunity to: * Provide strategic ... Direct experience with Immunohistochemistry (IHC) operational workflows * Ability to work in a ...

WuXi AppTec

Principal Pathologist

This role is either on-site at our Natick facility or remote (this determination will depend on ... Provide consultation to Study Directors on studies. * Ensure the compliance of various GLPs, comply ...

Miamioh

Education Abroad Advisor

Oxford, OH · On-site +1

$46K/yr

Align study abroad options with the Miami University curriculum by collaborating with academic ... Remote work at 20% per week is an option after a successful 6 month on-boarding period. Additional ...

Miamioh

$46K/yr

Align study abroad options with the Miami University curriculum by collaborating with academic ... Remote work at 20% per week is an option after a successful 6 month on-boarding period. Additional ...

Vrtx

HEOR Modeling Director (Remote-Eligible)

Boston, MA · On-site +1

$204K - $306K/yr

Provide input into design and interpretation of evidence generation studies needed to support ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

Inizio Evoke

Director, Analytics (Remote)

Chicago, IL · Remote

We study the 'why' behind health decisions and create creative solutions that inspire meaningful ... About the role The Director of Analytics is a senior analytics and marketing science leader ...

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Remote Study Director information

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$45K

$128.4K

$232.5K

How much do remote study director jobs pay per year?

As of Jun 29, 2026, the average yearly pay for remote study director in the United States is $128,367.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,500.00 per year, depending on experience, location, and employer.

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 the key skills and qualifications needed to thrive as a Remote Study Director, and why are they important?

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 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.
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Remote Study Director jobs near you
Senior Director, Clinical Sciences

Senior Director, Clinical Sciences

Amylyx Pharmaceuticals

Cambridge, MA • On-site, Remote

Other

Posted 13 days ago

Key responsibilities

  • Collaborates with the clinical development team in review, analysis, and interpretation of study results.

  • Provides scientific support on ongoing Phase I to III clinical trials and contributes to the planning and design of upcoming clinical studies.

  • Authors and/or reviews clinical trial-related documents including protocols, CRF, informed consent, protocol deviations, monitoring plans and regulatory documents.

Job description

The Opportunity

The Senior Director, Clinical Sciences will be a key member of the Clinical Development team with responsibilities to provide scientific support for ongoing activities. This role will report to a Senior Medical Director and will collaborate cross functionally with R&D, program management, clinical operations, biostatistics, and data management. The selected candidate will support and drive key development activities for clinical studies and overall execution of program Clinical Development Plans (CDP).

Responsibilities

  • Collaborates with the clinical development team in review, analysis, and interpretation of study results.
  • Provides scientific support on ongoing Phase I to III clinical trials and contributes to the planning and design of upcoming clinical studies.
  • Performs monitoring and review of study data including labs, safety data, and patient eligibility and consults with the program physician as needed.
  • Authors and/or reviews clinical trial-related documents including protocols, CRF, informed consent, protocol deviations, monitoring plans and regulatory documents, etc.
  • Contributes to regulatory documents including CSRs, Investigator's Brochures, and Clinical sections of INDs, CTAs.
  • Interacts with external medical/scientific advisors, thought leaders and clinical investigators in the therapeutic areas as well as with internal management and drug development staff to prepare/revise/maintain and efficiently execute the clinical development plan.

Required Qualifications

  • Advanced degree (., Ph.D., Pharm.D., Master's Degree in Science/Medical-related field). PhD or PharmD with 5+ years Clinical Research, Pharmaceutical, or CRO experience, OR Master's degree with 10+ years of relevant experience.
  • Knowledge of Phase 1-3 drug development.
  • Knowledge of clinical trial implementation and sponsor/site interactions for clinical trials.
  • Well-versed in relevant applications of GCP (Good Clinical Practice), ICH, FDA, EMEA and other relevant guidelines and regulations.
  • Strong, collaborative team-player.
  • Excellent attention to detail and communication skills.

Preferred Requirements

  • Prior experience working in rare disease within neurology or endocrinology

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

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