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Remote International Archivist Jobs (NOW HIRING)

Parexel

Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with ... Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. * Good ...

Jobgether

Maintain an organized archive of experiments, findings, and recommendations. * Proactively identify ... International and remote-first working environment with colleagues across different locations. How ...

SHI

Solutions Engineer - Data Engineering

$117K - $140K/yr

About Us Since 1989, SHI International Corp. has helped organizations change the world through ... This position is primarily remote, with a home office setup provided in accordance with company ...

Fujifilm

Account Manager

... data archival. As AI workloads drive data volumes to grow at an unprecedented pace, demand for ... This position is remote and based on the West Coast. Company Overview " At FUJIFILM North America ...

Fujifilm

Account Manager

... data archival. As AI workloads drive data volumes to grow at an unprecedented pace, demand for ... This position is remote and based on the West Coast. Company Overview" At FUJIFILM North America ...

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Remote International Archivist information

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$28.5K

$72.8K

$119K

How much do remote international archivist jobs pay per year?

As of Sep 3, 2026, the average yearly pay for remote international archivist in the United States is $72,781.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,500.00 and $83,500.00 per year, depending on experience, location, and employer.

What is a remote international archivist?

A Remote International Archivist is a professional who manages, organizes, and preserves historical documents and records for organizations across different countries, all while working remotely. They use digital tools to catalog, digitize, and maintain collections, ensuring the information is accessible and secure. This role often requires knowledge of archival standards, metadata, and digital preservation techniques, as well as strong communication skills for collaborating with international teams. Remote International Archivists may work for museums, universities, corporations, or government agencies with global operations.

What are the key skills and qualifications needed to thrive as a remote international archivist?

To thrive as a Remote International Archivist, you need expertise in archival science, records management, and metadata standards, typically supported by a relevant degree or certification such as a Master's in Library and Information Science (MLIS) or Certified Archivist credential. Familiarity with digital asset management systems, content management platforms, and data preservation tools is essential. Strong organizational skills, cultural sensitivity, and effective virtual communication are crucial soft skills for collaborating across global institutions. These competencies ensure the accurate preservation, accessibility, and integrity of archival materials in an international and remote context.

How does a remote international archivist typically collaborate with global teams to manage and preserve digital records?

As a Remote International Archivist, you will frequently coordinate with colleagues across different countries and time zones using digital communication tools. Collaboration often involves setting standardized metadata practices, sharing updates on records management, and troubleshooting access issues collectively. You'll participate in virtual meetings, contribute to cloud-based documentation, and ensure consistent archival processes globally. This role requires strong communication skills and adaptability to diverse cultural and organizational practices.

What is the difference between Remote International Archivist vs Remote Digital Archivist?

AspectRemote International ArchivistRemote Digital Archivist
CredentialsArchival certifications, MLS or MLIS, language skillsArchival certifications, MLS or MLIS, digital preservation skills
Work EnvironmentInternational institutions, cultural organizations, museumsLibraries, museums, corporate archives, digital repositories
Industry UsageGlobal cultural and historical institutionsTech companies, digital media, cultural institutions
Search IntentInternational archival roles, multilingual archivesDigital preservation, digital asset management

The Remote International Archivist typically works with global or multilingual archives in cultural or historical institutions, requiring language skills and international experience. In contrast, the Remote Digital Archivist focuses on digital preservation and asset management within digital or tech-focused environments. Both roles require archival credentials but differ mainly in their focus on physical versus digital collections and their work settings.

More about Remote International Archivist jobs

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Cities with the most Remote International Archivist job openings:

What are the most commonly searched types of International Archivist jobs?

The most popular types of International Archivist jobs are:

What states have the most Remote International Archivist jobs?

States with the most job openings for Remote International Archivist jobs include:

What job categories do people searching Remote International Archivist jobs look for?

The top searched job categories for Remote International Archivist jobs are:

Remote International Archivist jobs near you
Infographic showing various Remote International Archivist job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $72,781 per year, or $35 per hour.

Clinical Research Associate/Senior Clinical Research Associate- FSP

Parexel

Remote

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

32nd of 75 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.
Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred.
Job Purpose:
The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Key Accountabilities:
Site Management Responsibilities
  • Contributes to the selection of potential investigators.
  • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
  • Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
  • Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
  • Actively participates in Local Study Team (LST) meetings.
  • Contributes to National Investigators meetings, as applicable.
  • Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
  • Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
  • Updates CTMS and other systems with data from study sites as per required timelines.
  • Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
  • Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines, and discusses with LSAD the correct timing and type of visits.
  • Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
  • Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
  • Ensures data query resolution in a timely manner.
  • Works with data management to ensure robust quality of the collected study data.
  • Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
  • Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
  • Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
  • Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
  • Assists site in maintaining inspection ready ISF.
  • Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
  • Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
  • Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
  • Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
  • Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line manager.

Compliance with Sponsor Standards
  • Ensures compliance with the Client's Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).
  • Ensures compliance with local, national, and regional legislation, as applicable.
  • 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):
  • Excellent attention to detail.
  • Good written and verbal communication skills.
  • Good collaboration and interpersonal skills.
  • Good negotiation skills.
  • Proficient in written and spoken English language required.
  • Fluency in local language(s) required.

Skills (Desirable):
  • Ability to work in an environment of remote collaborators.
  • Manages change with a positive approach for self, team, and the business. Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
  • Good analytical and problem-solving skills.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.

Knowledge and Experience (Essential):
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
  • Good knowledge of relevant local regulations.
  • Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
  • Basic understanding of the drug development process.
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management.

Knowledge and Experience (Desired):
  • Familiar with risk-based monitoring approach including remote monitoring.
  • Good cultural awareness.

Education:
  • Bachelor's degree in related discipline, preferably in life science, or equivalent qualification (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/internationally as Required
  • Valid driving license per country requirements, as applicable.

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

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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