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Job Details

DEDICATED TO ONE SPONSOR - MOSCOW RUSSIA CRA!!!

Company: Just Pharma
Location:
Reference: sbrusscra
Closing Date: 05 Jan 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

A REALLY FANTASTIC OPPORTUNITY HAS LANDED ON JUST PHARMAS DESK! It's a great oppotunity for a CRA in the Moscow area to join an AWARD WINNING COMPANY!!

Requirements:

DEDICATED TO ONE SPONSOR

MOSCOW RUSSIA 

CRA / SCRA 

 

Responsibilities of the Clinical Research Associate:

Monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards, Declaration of Helsinki, Federal Regulatory Requirements and study procedures
Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
Assist with study protocol design, development and / or review if required
Complete and compile all necessary research, documentation and information to gain appropriate regulatory and ethical committee approval where required
Perform pre-study initiation, interim monitoring and close out visits as required
Carry out drug formulation administration procedures and documentation records
Ensure adequacy of drug shipment and drug accountability
Liaise with the Medical Monitor, Principal Investigator, clinical operations staff and sponsor representatives as required
Organise / attend investigator meetings as required
Provide support to the Project Manager / Country Manager with ad-hoc tasks as required

Essential Criteria:

Bachelors degree, equivalent or higher qualification within Medicine, Biological Science, Pharmacology, Nursing or a relevant life sciences discipline
Clear understanding of the drug development process
Significant experience in performing a Clinical Research Associate role
Work experience within either a hospital, medical / research centre environment, Contract Research Organisation or Pharmaceutical company
Proven track record of adherence to ICH-GCP and applicable local regulatory requirements during the conduct of clinical trials
Ability to contribute to the development of clinical trial related documents and materials
Ability to independently perform pre-study initiation, interim monitoring and close out visits as required
Good communication skills including the ability to present complex information to both clinical and non-clinical disciplines
Excellent presentation skills including the ability to meet exacting standards and a keen attention to detail
Fluency in English and Russian(both written and spoken)
Willingness and ability to travel
Willingness and ability to be Home based in Moscow, Russia

Desirable Criteria:

Experience across a wide range of clinical indications / therapeutic areas
Ability and experience to work with an electronic case report form (eCRF)
Membership of local professional bodies or international clinical groups
Ability to mentor, train, supervise and inspire confidence in newcomers to the industry

Apply for this job: DEDICATED TO ONE SPONSOR - MOSCOW RUSSIA CRA!!!

Contact Information:

Address:  Head Office
2nd Floor Albany Chambers, Bridge Road East, Welwyn Garden City, Hertfordshire
AL7 1HL
England
Tel:  0044 1707 830300
Website:  Visit Our Web Site

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