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The Study Pro Jobs (NOW HIRING)

Parexel

Local Study Associate Director- FSP

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 ...

Parexel

Local Study Associate Director- FSP

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 ...

Stantec

Study Manager

Chandler, AZ · On-site

The Study Manager is the principal liaison between Stantec and the client during the planning and ... Actual compensation for part-time roles will be pro-rated based on the agreed number of working ...

Stantec

Study Manager

Tucson, AZ · On-site

The Study Manager is the principal liaison between Stantec and the client during the planning and ... Actual compensation for part-time roles will be pro-rated based on the agreed number of working ...

Stantec

Study Manager

Chandler, AZ · On-site

The Study Manager is the principal liaison between Stantec and the client during the planning and ... Actual compensation for part-time roles will be pro-rated based on the agreed number of working ...

NYULMC

Research Data Associate

New York, NY · On-site

In this role, the successful candidate Responsible for providing direct data and/or clinical research in support of clinical trials, studies and general research under direct supervision. Works with ...

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How much do the study pro jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for the study pro in the United States is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $25.00 per hour, depending on experience, location, and employer.

What is a Study Pro?

A Study Pro is an educational coach or tutor who specializes in helping students develop effective study habits, executive function skills, and academic strategies. They work with students to improve organization, time management, goal setting, and test preparation. Study Pros may also support students with learning challenges by providing personalized guidance and accountability. Their goal is to empower students to become independent, confident learners.

How does a Study Pro typically collaborate with students, parents, and educators to support academic success?

A Study Pro works closely with students to develop effective study habits, time management skills, and personalized learning strategies. They regularly communicate with parents to provide updates on progress and suggest ways to reinforce positive habits at home. Additionally, they may collaborate with teachers or school counselors to align their support with classroom expectations and address specific academic challenges. This collaborative approach helps ensure that each student receives comprehensive support tailored to their unique needs.

What are the key skills and qualifications needed to thrive as a learning coach at The Study Pro, and why are they important?

To thrive as a Learning Coach at The Study Pro, you need a background in education or child development, strong organizational skills, and experience supporting students' academic growth. Familiarity with digital learning platforms, progress tracking tools, and educational software is often required. Exceptional communication, patience, and the ability to motivate and engage students are critical soft skills in this role. These skills ensure effective personalized support, foster student independence, and help learners achieve academic success in a structured environment.

What is the difference between The Study Pro vs Academic Tutor?

AspectThe Study ProAcademic Tutor
CredentialsVaries; often requires subject expertise or certificationsTypically requires a degree or ongoing education in the subject
Work EnvironmentOnline or in-person sessions, flexible hoursIn-person or online, often one-on-one sessions
Industry UsageEducational support, test prep, skill developmentAcademic assistance, homework help, exam prep

The Study Pro and Academic Tutor both provide educational support, but The Study Pro often offers more flexible, broader services including test prep and skill development, while Academic Tutors focus primarily on subject-specific assistance. Both roles require relevant knowledge and certifications, with work environments ranging from online to in-person sessions.

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What states have the most The Study Pro jobs?

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The Study Pro jobs near you
Infographic showing various The Study Pro job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $47,067 per year, or $22.6 per hour.

Local Study Associate Director- FSP

Parexel

Remote

Full-time

Re-posted 18 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 74 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..

#LI-KW1
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

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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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