Clinical Trial Analyst, Europe job in Warsaw, Poland

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First Name*

Last Name*

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Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Clinical Trial Assistant (CTA)

Location: Poland

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting a Clinical Trial Analyst, Europe for a CRO. This role is on a permanent basis and allows for remote based working within Europe. The client is focused on assisting their clients to offer remedies to people who need them the most.

Responsibilities:

Responsible for all technology set-up for allocated trials which involve collaborating with associates across various divisions who have particular duties for part of the set-up.
Raise requests or needs for non-standard technology to the allocated client technology partner.
When suitable, set-up trial technologies.
Train and guide more junior personnel.
Guarantee the quality, deadlines, and budget linked to the trial technology meets the project needs.
Act as the main point of contact with the project team for trial-level technology, and data integration solutions, covering CRS, PI, IT and technology third party suppliers.
You will manage outlining and documenting needs for the trial technology.
Warrant project satisfaction of the trial technology solution.
Other duties may be assigned to this role.

Skills & Requirements:

Educated to a degree level in a life science, computer science or similar discipline.
Capable of handling competing priorities independently with a high attention to detail.
Acquaintance with organising teams and gathering necessities.
Able to motivate and work efficiently in virtual teams within different cultural settings.
To accomplish outcomes, you will be able to deliberate and inspire others.
Familiarity with technical and data standards.
Prior involvement with clinical trial systems such as CTMS, EDMS, EDC, IVRS, documenting tools, etc., and in configuration of these systems.
Conscious of CRS, PI and supplier software and tools on an external basis, with know-how of how these applications operate, as well as offer effectiveness to operations.
Capable of being adept to learning new systems and operate in a developing technical setting.
You are conscious/experienced in the requirements and use of data standards within clinical trial settings such as CDISC, SDTM, if applicable.
Comprehension of clinical trial procedurs.
Know-how of SOPs/regulations/systems of life cycle strategies, ICH-GCPP and any other suitable regional and global guidelines, for example: 21 CFR Part 11 and demonstrated practical application.
Committed to quality, quality management and operational efficacy.
Flexible to modifications.
Client oriented both internally and externally, with the ability to communicate both verbally and in writing.
Fluency in the English language.
Former involvement in a clinical trial organisation, with a comprehension of the process steps and contributors included.
Exhibited the ability to inspire a team to deliver rendering to a timetable.
Familiarity with configuring technology for clinical trials though systems development experience is not necessary for the role.
Acquaintance with data standards organisation such as CDISC, HL7 on an external level would be beneficial for the role, but not essential.

If you are having difficulty in applying or if you have any questions, please contact Harry Qureshi at +44 203 949 8646.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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