Experienced Clinical Research Associate, Ukraine

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits

• Supporting the development of a subject recruitment plan

• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines

• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions

• Collaborating with experts at study sites and with client representatives

Qualifications:

• University degree in scientific discipline or health care

• Requires 2-3 year of on-site monitoring experience.

• Very good computer skills including MS Office

• Excellent command of Ukranian and English language.

• Organizational, time management and problem-solving skills

• Ability to establish and maintain effective working relationships with coworkers, managers, and clients

• Flexibility to travel

• Driver’s license class B

What you can expect:

• Resources that promote your career growth

• Leaders that support flexible work schedules

• Programs to help you build your therapeutic knowledge

• Excellent working environment in a stabile, international, reputable company

• Company car or car allowance, mobile phone and attractive benefits package

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