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Senior Clinical Project Administrator
Labcorp
Place of work
Prague
Prague
Contract type
full-time
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
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!
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.
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
- 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
2016-04-13
lokalita: Prague Pozice: Clinical Data Manager, Project Manager, Regulatory Affairs Manager, Regulatory Affairs Specialist Společnost: Labcorp