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Job Details

Site Manager

Company: Docs Global (Continental Europe)
Location: Budapest,Hungary
Reference: Ref AS-027904
Closing Date: 19 Feb 19
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

As a driven person who has the ambition to achieve you will be given the opportunity to gain more responsibilities and enhance your professional profile Please send CV to me 0036703831286


Roles & Responsibilities of the position

1. Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team
2. Acts as primary local company contact for assigned sites for specific trials.
3. Attends/participates in investigator meetings as needed.
4. Responsible for executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs/WIs/IFUs and policies.
5. Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases
6. Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.
7. Ensures site study supplies (such as Non-IP, lab kits, etc.) are adequate for trial conduct.
8. Ensures that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented.
9. Arranges the appropriate destruction of clinical supplies
10. Ensures site staff complete the data entry and resolve queries within expected timelines.
11. Ensures accuracy, validity and completeness of data collected at trial sites
12. Ensures that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs, ensure that they are consistent with all data collected and with the information in the source documents.
13. Maintains complete, accurate and timely data and essential documents in systems utilized for trial management (e.g. CTMS, eTMF/IF, Trial Master Source and Sharepoints.
14. Fully documents trial related activities in particular monitoring. Writes visit reports and uploads into eTMF within 5 working days for review and approval. Complete follow-up letter to communicate relevant information and required corrective action to the investigator

Job Requirements

A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred. A minimum of 1 year of clinical trial monitoring experience is preferred.
Good working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
Good IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
Proficient in speaking and writing the country language and English. Good written and oral communication skills.

Remuneration & other details

Working for one of the top pharmaceutical companies within a stable team. Depending on the level of your experience, you will have the possibility to develop your therapeutic are experience and monitoring skills. Competitive remuneration and possibility to develop your career in a dynamic environment with the support of our CTM.

Apply for this job: Site Manager

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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