Sponsor Dedicated CRA II - Home Based ITA

Description
Sponsor Dedicated CRA II - Home Based ITA
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
What Makes This Role Unique?
This is a Sponsor Dedicated / FSP position, meaning:

• You will be afull Syneos Health employee, working exclusively with one of our strategic pharmaceutical partners.
• You’ll have aSyneos Line Managerguiding your career journey—performance reviews, 1:1s, development plans, and workload support.
• Enjoy the best of both perspectives:immersed in the sponsor’s clinical environment, while receivingongoing training, onboarding, and career supportfrom Syneos Health.
  

Your Impact
As a CRA II, you’ll be theeyes and ears on the ground , ensuring clinical trials run smoothly and ethically. You’ll:

• Conducton-site and remote monitoringof clinical studies.
• Review protocols, informed consent forms, and case report forms.
• Ensure compliance withGood Clinical Practice (GCP)and regulatory standards.
  

What The Sponsor Is Looking For

• Asite engagerwho builds strong, trust-based relationships with local sites.
• Solid understanding ofGCP guidelinesand regulatory frameworks.
• Excellent communication skills andproficient Englishto collaborate across teams.
  

What You Bring

• Minimum 2 yearsas a Certified CRA (per DM 15 Nov 2011).
• Based in awell-connected Italian city, working fully remote.
  

Therapeutic Areas You’ll Explore

• Neurology
• Autoimmune diseases
• Dermatology/respiratory
• Rare diseases
  

What does it mean to join us?
At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance.
Besides competitive compensation packages, you’ll find:

• A truly collaborative culture - every team member is valued, heard, and empowered to share ideas for constant improvement and innovation.
• Annual performance reviewswith potential for merit increases and promotions.
• Continuous trainingand career development support thanks to your dedicated Line Manager.
• Global mobility: working from abroad in countries with Syneos legal entities (upon approval).
• Access to our global mental health and wellbeing program—for you and your loved ones.
• Access to industry leading technology and solutions, in collaboration with global teams
• Spotlight to give peer-to-peer recognition and for you to be rewarded for your service and achievements.
• please note that the Therapeutic areas reported may change according to Sponsor’s needs
  

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.
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 are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. 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. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.