Clinical Research Associate (Client Onsite) - CRA - Moscow, Saint Petersburg

Вакансия № 5765992 от компании PPD на Электронной Службе Занятости Населения Москвы.

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☑ Основной блок:

Опыт работы: 1–3 года.

Тип занятости: полная занятость.

График работы: полный день.

Зарплата: по результату собеседования.

Примерное место работы: Россия, Москва.

☑ Актуальность объявления:

Это объявление № 5765992 добавлено в базу данных: Среда, 5 марта 2025 года.

Дата его обновления на этом интернет-ресурсе: Воскресенье, 16 марта 2025 года.

☑ Статистика предложения работы № 5765992:

Прочитано соискателями - 200 раз(а);
Отправлено откликов - 0 раз(а);

☑ Репутация компании "PPD":

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☑ Подробности о вакантном месте:

PPD has an exciting opportunity for a CRA to join us onsite exclusively for one of our strategic pharmaceutical partners in Russia. PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD.

This is a great opportunity for CRAs at any level currently working within the life science sector for pharmaceutical companies, Biotech companies or CROs who would enjoy the opportunity to work for a CRO dedicated to one client.

As the trusted partner of some of the most innovative big pharma and biotech companies; our CRAs have the opportunity to work on challenging projects across a wide range of therapy areas. Our vision is to be the global leader in our industry; based on consistent quality and execution, exceptional customer-aligned service and constant innovation.

You should thrive in project teams and be focused on delivering exemplary levels of customer service. You will have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work.

You will perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.

In return we will offer you a positive and supportive working environment within one of the most engaged teams in the industry; who are truly recognised as the cornerstone of our success. We will provide you with meaningful work and the opportunity to acquire valuable personal and professional skills.

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.

With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

Education and Experience:

• Degree in pharmacy, life science or related field

Knowledge, Skills and Abilities:

Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Effective independent clinical monitoring skills;
Excellent understanding and demonstrated application of GCPs and applicable SOPs
Management of regulatory and / or IEC questions
Development and preparation of the local informed consent form
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Management of the delivery of study supplies
Strong customer focus
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Proven flexibility and adaptability
Ability to work in a team or independently as required
Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

PPD Offers:

As an equal opportunity employer. PPD believes that employees are the key to its success, and is committed to your professional growth. We offer an attractive salary, comprehensive benefits package as well as personal development and training programs.