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Job Details

SCRA - CNS - Italy

Company: Syneos Health
Reference: 17006050
Closing Date: 12 Apr 18
Type: Permanent
Salary (£): Negotiable

Job Summary:

Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.


We are currently looking to strengthen our Clinical Monitoring team in Italy and are seeking an experienced Clinical Research Associate for our CNS Business Unit to be based from our office in Saronno (we can consider home based workers as well).


 At Syneos Health, we appreciate the complexities of the nervous system and the widely varying disciplines that explore CNS function, dysfunction and drug research. Working with CNS specialists and drawing upon an extensive network of academic and private physician investigators, we have directed clinical trials for more than 20 years in analgesia, neurology, psychiatry and ophthalmology, earning worldwide recognition as leaders in CNS drug and product development.


Core responsibilities:
A brief summary of duties you will be involved in:
- Completing project activities associated with monitoring functions of Phase I-IV clinical research studies.

- Performing monitoring functions to assess the progress of clinical studies at assigned investigative sites (either on site or remotely) to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.




To succeed in this role you will need the following skills/experience:
- BA/BS degree in science/health care field or nursing degree or equivalent combined education and experience.
- Understanding of SOPs, WIs, FDA and local regulations as well as ICH-GCP guidelines.
- Demonstrates ability to prioritize and manage time for the preparation, completion and follow up of monitoring tasks.
- On site experience with most types of visits; PSSV, SIV, IMV, COV.
- Effective command of written and spoken English language.


What happens next:
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.


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. #LI-JR1

Apply for this job: SCRA - CNS - Italy

Contact Information:

Address:  European Head Office
River View, The Meadows Business Park, Station Approach, Blackwater, Surrey
GU17 9AB
Tel:  +44 (0) 1189 335 300
Website:  Visit Our Web Site

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