Description

Sponsor dedicated CRA ll/Sr CRA I - Home-based Israel

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

Clinical Research Associate (CRA II, or Senior CRA I, based on your experience)

This role offers a permanent contract with Syneos Health, it is dedicated to one big global pharma sponsor. In terms of benefits to support you with your monitoring visits, you can choose between either a company car, or a car allowance.

Syneos Health is looking for an experienced Clinical Research Associate to work within the team of our global Pharma client. The role is permanent and fully dedicated to one sponsor.

As a Clinical Research Associate you will be responsible for the full range of activities from study set-up through to close-out.

Responsibilities:

Assess potential investigators and decide on the suitability of the site.
Develop/adapt recruitment and retention strategy for the site.
Ensure that the current versions of the trial documents that are listed on the Site Initiation Report and all required trial-related materials and supplies are provided to the investigational site.
Negotiate investigator budgets at site level and track the status of site CTA.
Plan and conduct investigator and site-staff training.
Conduct site initiation, monitoring and closure visits.
Create site specific and monitoring tools.
At the investigational site, ensure clinical drug supplies are available, appropriately used, handled, stored (e g, temperature logs, security), and returned, accurately inventoried and documented.

Qualifications

What we’re looking for

Previous on-site monitoring experience in Israel is a must, with min 2 years in a CRA role.
Experience with Oncology/ Hemato-Oncology studies is an advantage, but not required.
You must be fluent in Hebrew as well as a good level of English.
You should be ready to frequent business trips (75% of time).
You should have strong communication and interpersonal skills, a motivation towards strong team work and enjoy building relationships.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education.Impact and ContributionRoles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes.Core Focus•Conduct thorough on-site and remote monitoring of clinical research studies•Develop and implement tools, procedures, and processes to ensure quality monitoring•Manage defined components of projects or processes within their area of responsibility•Utilize practical knowledge of a professional area, typically obtained through education combined with experience•Maintain high standards of clinical practice and ensure the success of clinical trials