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Job Details

Clinical Research Associate (office based- Warsaw)

Company: Docs Global (Continental Europe)
Location: Warsaw,Poland
Reference: Ref AS-024270
Closing Date: 24 Mar 18
Type: Permanent
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

DOCS is supporting highly prestigious and one of the world’s top pharmaceutical company that is bringing innovative ideas, products and services continuously improving people’s health. This is a fantastic opportunity for an experienced clinical research professional that is ready to take on a new challenge, further develop their career and enjoy working culture in vibrant Client's office in Warsaw.

Requirements:

Roles & Responsibilities of the position

The Clinical Research Associate (CRA) acts as site manager between site staff and Pharmaceutical Company, working within Polish Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for tangible trial operational targets (KPIs) and ensuring the highest possible data quality in clinical trial(s). The position is based in Warsaw, reports to Clinical Team Leader, Poland and will require travelling up to 60% of the time.

Essential responsibilities
•The primary point of contact between site staff and Client
•Leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, Client procedures and protocol requirements to ensure data quality and study subject protection
•Managing the site to meet patient recruitment rate and target
•Delivery of results that have direct impact on the successful completion of the clinical programme
•Communication about progress and critical issues that may impair trial progress to Local trial Manager (LTM) and/or Regional Trial Manager (RTM)

Job Requirements

•Bachelor or master degree in Life Sciences or equivalent
•Experience as CRA or in-house CRA in the pharmaceutical industry or Clinical Research Organisation (CRO), preferably 1-2 years
•Ability to build and maintain relationships with sites
•High focus on delivery and quality
•Excellent communication and negotiation skills
•High degree of trustworthiness
•Adequate English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports
•IT proficiency
•Proven decision making and problem solving capabilities
•Ability to manage multiple priorities
•Team oriented personality with high degree of flexibility
•Ability and willingness to adjust quickly to new situations in a continuously developing environment
•Act as an ambassador of the company
•Flexibility is very important due to the large number of minor and major tasks coming from different customers

Remuneration & other details

A challenging role in international Pharmaceutical company.
•Permanent office based position (direct hire) in a stable organization.
•You will enjoy highly competitive compensation and an exceptional benefits package (company car, mobile phone, health& life insurance, lunch vouchers, bonus)

To apply:
For an immediate consideration please contact Dagmara Drozdowska on: +48 668 87 02 61or email your CV (WORD file) to: dagmara.drozdowska@docsglobal.com

Apply for this job: Clinical Research Associate (office based- Warsaw)

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

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