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Remote Study Director Jobs (NOW HIRING)

Parexel

Local Study Associate Director- FSP

This is a remote role. Oncology experience is required for this role and cell therapy is strongly preferred! The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country ...

U.S. Fish and Wildlife Service

Biologist

Grand Junction, CO · On-site +1

$50K - $80K/yr

Travel to remote study sites may be required via boats, small aircraft, snowmobiles, all-terrain ... Direct Deposit participation required. * Successfully pass the E-Verify employment verification ...

New

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 ...

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 ...

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 ...

Emmes

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... We believe the work we do will have a direct impact on patients' lives and act accordingly. We ...

Centene

Remote Medical Director, Appeals

OR · On-site +1

$236K - $449K/yr

Identifies utilization review studies and evaluates adverse trends in utilization of medical ... with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an ...

Kinectrics

Director - Power Systems Studies

Director - Power System Studies Employment Type: Full-Time Employment Level: Senior Location ... Remote, United States Department: Grid and Generator Services Reports to: Vice President , Grid and ...

Recursion

Director, Clinical Science

New York, NY · Remote

$212K - $261K/yr

As a Director within Clinical Science, you'll play a critical role in ensuring study protocols are ... This is a fully remote opportunity with occasional travel requirements. Travel may be necessary ...

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Remote Study Director information

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$45K

$128.4K

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How much do remote study director jobs pay per year?

As of Aug 15, 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?

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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What states have the most Remote Study Director jobs?

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Remote Study Director jobs near you
Infographic showing various Remote Study Director job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 6% In-person, and 94% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.

Local Study Associate Director- FSP

Parexel

Remote

Full-time

Re-posted 8 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 73 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
PXL FSP is seeking LSADs in the US! This is a remote role. Oncology experience is required for this role and cell therapy is strongly preferred!
The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.
The LSAD may perform site monitoring as needed to support the flexible capacity model.
The LSAD is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.
Trial and Site Administration
  • Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
  • Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies.
  • Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH-GCP and local regulations.
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
  • Plans and coordinates applicable to local drug activities (from local purchase or reimbursement to drug destruction).
  • Sets up and maintains the study in CTMS at study country level and local websites as required by local laws and regulations.
  • Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.
  • Reviews monitoring visit reports (as required and following Client SOPs) and pro-actively advises the monitor(s) on study related matters.
  • Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs.
  • Proactively identifies risks and facilitates resolution of complex study problems and issues.
  • Organizes regular Local Study Team meetings on an agenda driven basis.
  • Actively works towards achieving good personal relationships with all Local Study Team members, sites' staff and global stakeholders.
  • Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead.
  • Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.
  • Develops, maintains and reviews risk management plans on country study level; proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.
  • Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.
  • Plans and leads National Investigator meetings, in line with local codes, as required.
  • Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies.
  • Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and client Procedural Documents.
  • Plans and leads activities associated with audits and regulatory inspections in liaison with Clinical Quality Associate Director (CQAD) and QA.
  • Provides input to process development and improvement.
  • Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues.
  • Updates Line Managers about the performance of the CRAs/CSAs.
  • Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
  • Collaborates with local Medical Affairs team.
  • Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management

Document Management
  • Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant client SOPs and local regulations.
  • Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with Client SOPs.
  • Ensures completeness of the eTMF and ensures essential documents are uploaded in a timely manner to maintain the eTMF "Inspection Ready".
  • Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.

Regulatory and Site Start Up Responsibilities
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.
  • Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organized at country level.

Budgeting, Agreements and Payments
  • Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in client clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head).
  • Ensures timely preparation of local Master Clinical Study Agreement (CSA) (including site budget) and amendments as needed.
  • Ensures accurate payments related to the study are performed according to local regulations and agreements.

Compliance with Sponsor Standards
  • Ensures compliance with Client's Code of Ethics and company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).
  • Ensures that study activities at country level comply with local policies and code of ethics.
  • Completes timesheets accurately as required.

Compliance with Parexel Standards
  • Complies with required training curriculum.
  • Completes timesheets accurately as required.
  • Submits expense reports as required.
  • Updates CV as required.
  • Maintains working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements.

Skills (Essential):
  • Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
  • Excellent project management skills.
  • Excellent team building and interpersonal skills.
  • Excellent organizational skills.
  • Excellent verbal and written communication skills.
  • Excellent ability to prioritize and handle multiple tasks.
  • Excellent attention to detail.
  • Proficient in written and spoken English language required.
  • Fluency in local language(s) required.
  • Good negotiation skills.
  • Good ability to learn and to adapt to work with IT systems.

Skills (Desirable):
  • Good analytical skills.
  • Good resource management skills.
  • Good decision making and delegation skills.
  • Good financial management skills.
  • Basic change management skills.
  • Basic coaching skills.
  • Basic ability in handling crisis situations.

Knowledge and Experience (Essential):
  • Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies).
  • Good knowledge of international guidelines ICH GCP as well as relevant local regulations.

Knowledge and Experience (Desirable):
  • Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
  • Good knowledge of the Drug Development Process.
  • Excellent understanding of the Clinical Study Process including monitoring.
  • Very good understanding of the Study Drug Handling Process and the Data Management Process.
  • Good intercultural awareness.

Education:
  • Bachelor's degree in related discipline, preferably in life science, or equivalent qualification (or equivalent adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.

Other:
  • Ability to travel nationally and internationally as required.
  • Integrity and high ethical standards..

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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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