Site Management Associate I at PSI CRO

Capital City of Prague, Prague, Czechia -

Full Time

Start Date

Immediate

Expiry Date

19 Apr, 26

Salary

0.0

Posted On

19 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Organizational Skills, Planning Skills, Problem-Solving, Flexibility, Detail-Oriented, Multi-Tasking, Customer Service, Interpersonal Skills, Team-Oriented, Administrative Skills, Clinical Research, Document Management, Communication, MS Office Proficiency, Czech Proficiency, English Proficiency

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 more than 3.000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Site Management Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies Assists with handling administrative financial tasks Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections Other Communication Exchanges data, documents, and other information with the project team and other departments Provides assistance with organization of internal team meetings Prepares draft minutes of internal team meetings Assists with preparation, attendance and follow-up of Investigator’s Meetings, as applicable Under supervision, maintains study-specific and corporate tracking systems Document Management Maintains Trial Master File (TMF) Perform TMF review and oversight at country and site level Prepares, distributes, and updates Onsite Study Files (OSF) and OSF checklists Provides assistance with translations Qualifications College/University Degree (Life Sciences) Full working proficiency in Czech and English Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting Proficiency in standard MS Office applications 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 Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Responsibilities

The Site Management Associate I will support clinical research projects by managing communication, documents, and information. Responsibilities include maintaining the Trial Master File, coordinating audits, and assisting with administrative tasks.