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PSI CROPC

Legal Administrative Assistant

PSI CRO is a global, full-service Contract Research Organization (CRO) founded in 1995, specializing in predictable patient enrollment and on-time delivery of clinical trials across various therapeutic areas. Headquartered in Switzerland, PSI operates in over 50 countries with a strong focus on quality and client satisfaction.

PSI CRO

Employee count: 1001-5000

Romania only

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Provide comprehensive administrative support to the Global Legal Manager and Legal Department, supports and coordinates contracting QC and execution formalities, intermediates legal administrative matters, coordinating with MO1’s various department stakeholders, ensuring smooth execution of legal department workflows: document preparation, contract lifecycle administration, quality control, coordination of translations and submissions, and basic legal research.

Key Responsibilities

  • Document Finalization and Formatting. QC check and finalise legal documents (contracts, amendments, templates, policies) in strict compliance with MO1 house style. Maintain document templates for recurring workflows.
  • Track Changes and Redlining. Process, consolidate, and clean redlined documents. Prepare blackline comparisons.
  • Contract Lifecycle Administration. Maintain the contracts log and repository, tracking key elements, circulate documents for review and signature, file executed agreements.
  • Quality Control. Verify defined terms, cross-references, formatting, completeness and accuracy of customizations, including schedules/annexes, prior to finalisation. Flag and correct discrepancies.
  • Basic Legal Research. Conduct targeted desktop research on regulatory and legal topics as directed. Present findings in concise summary format.
  • Translations and Administrative Filings. Coordinate translation workflows (internal/external). Handle routine filings, notarisations, apostilles, and regulatory submissions as instructed.
  • Education: Bachelor’s degree in law (strongly preferred). Related degrees (public administration, business, international relations) accepted if experience requirements are met.
  • Experience (mandatory): Minimum 2 years as a paralegal, legal assistant, or equivalent legal support role in a law firm, legal department, or professional services environment. International/multi-jurisdictional contract experience is a strong advantage.
  • Technical Skills (mandatory): Expert-level Microsoft Word (styles, Track Changes, document comparison, advanced formatting). Proficient in MS Office Suite (Excel, Outlook, PowerPoint, Teams) and SharePoint.
  • Language (mandatory): English C1 or above (working language of the department). Romanian native/fluent. Additional languages are an advantage.

Personal Competencies: Exceptional attention to detail. Strong organisational skills and ability to manage concurrent tasks. Self-motivated, reliable in a remote setting. Discretion with confidential information.

If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you.

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.

About the job

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Posted on

Job type

Full Time

Experience level

Education

Bachelor degree

Experience

2 years minimum

Experience accepted in place of education

Location requirements

Hiring timezones

Romania +/- 0 hours

About PSI CRO

Learn more about PSI CRO and their company culture.

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We are a leading full-service global Contract Research Organization (CRO) with a key strength in predictable patient enrollment across multiple therapeutic areas. Since our founding in 1995 by Dr. Robert Reekie and Dr. Roger A. Smith, we've been dedicated to revolutionizing how clinical trials are conducted, focusing on delivering high-quality, cost-effective solutions worldwide. Our mission is to be the best CRO in the world as measured by our employees, clients, investigative sites, and vendors. This commitment is reflected in our exceptionally high repeat and referral business rates and minimal staff turnover.

Our global reach allows us to conduct clinical trials across multiple continents and in over 50 countries. We are known in the industry for our 'on-time project delivery,' a reputation we've built by investing substantial effort and medical expertise into performing quality feasibility assessments that provide accurate predictors of study timelines. In fact, over 90% of our studies finish on time or ahead of schedule. We specialize in planning and executing global pivotal registration clinical trials, particularly in complex areas like oncology, hematology, infectious diseases, gastroenterology, multiple sclerosis, and rare indications. We embrace innovation and technology, leveraging cutting-edge methodologies and data-driven insights to optimize trial design, streamline operations, and enhance patient engagement. Our robust quality management systems and adherence to the highest industry standards, including ISO 9001:2015 and ISO 27001:2013 certifications, underscore our dedication to excellence. We are proud of our contributions to advancing healthcare by helping bring life-saving therapies and treatments to market. We actively engage in research collaborations and knowledge sharing to contribute to scientific advancement.

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PSI CRO

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