Senior Clinical Project Administrator

Labcorp

Place of work
Prague
Contract type
full-time

Information about the position

Job description, responsibilities and duties

COVANCE is one of the world’s most comprehensive and experienced contract research organizations (CROs) with a tradition of innovation in the science and processes of drug development. We have the ability to offer wealth of services covering all aspects of drug development ranging from non-clinical research services through to post-marketing safety and commercialization services. We are currently the only CRO with this depth of service offerings.

We are currently recruiting a Senior Clinical Project Administrator to join our CoSourse team in Prague.

Responsibilities:

- Train and mentor Clinical Project Administrators
- Provide clerical support to project team (e.g., word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
- Set up and maintain clinical investigator files and documentation
- Prepare study-related documents and other materials for delivery to archives, at appropriate intervals
- Prepare investigator budget payments and tracking systems; generate tracking reports as assigned
- Prepare monitoring visit documentation for Clinical Research Assistants and above, as requested by supervisor
- Data entry and maintenance of selected study tracking data
- Assist with coordinating vendors
- Organize/prepare for client meetings/teleconferences
- Assist/prepare for client or internal audits
- Provide telephone coverage and related support duties
- Perform other administrative duties as assigned by management

Employee perks, benefits

We offer:

Covance's ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time to join us!

Information about the selection process

How to apply:

If you are interested in a Covance opportunity and would like to apply, please visit our website at covancecareers.com and look for the reference 60055BR.
You can also follow the link:
http://careers.covance.com/job-postings/60055BR/senior-clinical-project-administrator

Key Words: CPA, CTC, assistant, clinical administrator, project assistant, clinical trials, Prague, czech Republic

EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.

Requirements for the employee

Candidates with education suit the position

University education (Master's degree)

Language skills

English - Upper intermediate (B2) or Czech - Upper intermediate (B2)

Personality requirements and skills

Required skills, Experience and education:

- min 2 years experience in clinical trial field (previous Clinical Monitoring Assistant or similar experience)
- very good PC systems skills (excel, world, power point) plus CTMS
- fluent English both spoken and written, additional language is an asset
- Czech native
- excellent organizational and communication skills
- knowledge of CT local regulation and GCP

Advertiser

Brief description of the company

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ID: 2515591  Datum zveřejnění: 13.4.2016