Site Management Associate (Clinical Trial) at PSI CRO

Bangkok, , Thailand -

Full Time

Start Date

Immediate

Expiry Date

08 Jun, 26

Salary

0.0

Posted On

10 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Database Maintenance, Tracking Systems, Vendor Management, Study Supplies Management, Access Management, Document Processing, Filing, Communication, Query Resolution, Project Training, Payment Administration, Mail Handling, Meeting Arrangements, Agenda Preparation, Minute Taking, Organizational Skills

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications. 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 more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Job Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. The scope of responsibilities will include: Maintenance of databases and tracking systems. Serves as the primary sites’ contact point for vendors, study supplies, and access management. Work with large amount of documents, including their compiling, procurement, processing and filing. Communication with company departments and external parties. Communication point for investigative sites participating in the clinical research projects. Coordination of site-specific query resolution, project training and access to vendor-related systems for site teams. Ensures proper administration of sites and vendors payments. Receiving and routing all mails and incoming calls. Assistance with meeting arrangements. Preparation of draft agendas and minutes of project meetings. Qualifications College/University Degree (Life Sciences) Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting. Good organizational and planning skills, problem-solving abilities, flexibility. Detail-oriented, able to multi-task and work effectively in a fast-paced environment. Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects. Ability to speak Thai and English. Additional Information Take the next step in your career and join a company that genuinely focuses on its people. Being a Part of the Team As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback. Growth Opportunities PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.

Responsibilities

The Site Management Associate will serve as the key support for clinical research projects by streamlining communication, maintaining tracking systems, and managing essential documents and information flow. Responsibilities include acting as the primary contact point for sites regarding vendors and supplies, coordinating query resolution, and ensuring proper administration of site and vendor payments.