Document Management Specialist (Clinical Trial) at PSI CRO

Bangkok, , Thailand -

Full Time

Start Date

Immediate

Expiry Date

23 Mar, 26

Salary

0.0

Posted On

23 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Document Management, Communication, Collaboration, Detail-Oriented, Organizational Skills, PC Skills, MS Word, Excel, PowerPoint, English, Thai, Japanese

Industry

Pharmaceutical Manufacturing

Description

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients. We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here. Job Description If you are keen to provide administrative, document management support to pharmaceutical research projects, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you! The scope of responsibilities will include: Review, maintain and archive essential study documents for the Trial Master File Communication with multi-functional project teams on document management matters Qualifications Experience in document management activities is a plus. Fresh graduate are welcome to apply. Higher Vocational Certificate (e.g., Marketing, General Management, or Secretarial Studies). Full working proficiency in English and Thai. Knowledge of any other language spoken in Asia & Pacific region, especially Japanese is a plus. Detail-oriented mind-set and organizational skills. PC skills to be able to work with MS Word, Excel and PowerPoint. Communication and collaboration skills. We encourage junior candidates to apply for this position. Additional Information We offer: Excellent, flexible working conditions Extensive training and supportive team Competitive salary and benefits package Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.

Responsibilities

The Document Management Specialist will review, maintain, and archive essential study documents for the Trial Master File. They will also communicate with multi-functional project teams on document management matters.