About us
Sintesi Research is a full-service
Contract Research Organization (CRO)
founded in 2005 in Italy
Contract Research Organization (CRO)
founded in 2005 in Italy
Lead Clinical Research
On time On budget
- Sintesi Research provides full services or single activity according to the client needs, for multi-country clinical trials, including innovative approaches to the increasing complexity and variety of current projects, mostly in ethic products, medical devices and advanced therapies, no-profit Investigator Initiated Trials (IITs), epidemiologic/observational.
- Sintesi Research expertise is covering all phases of drug related trials, in several therapeutic area.
- Sintesi Research also manage clinical trials for nutraceutical studies and compassionate use programs.
- Operational staff include medical writers, regulatory experts, project managers, clinical monitors, data managers, statisticians, safety officer and quality assurance
Why Sintesi Research?
Expert CRO delivering tailored solutions
Partnering with SR Clinical provides you with an expert contract research organization that performs all clinical research activities on a global level.
We provide customized solutions, not a one-size-fits-all. We can take care of your complete clinical program from STUDY DESIGN to CSR or support you with very specific tasks within your clinical trials.
Given the complex nature of the processes from pre-clinical to post-approval of your product, SR understands that your needs have the priority.
We will focus our services to your timing, budget and needs.
Locations
-
Milano (ITALY) HEADQUARTERS
Via private delle Stelline 9 -
Barcelona (SPAIN)
Paseo de Maragall 23, 08026 -
Tel Aviv (ISRAEL)
Azrieli Towers Harokmim St. 26 Holon -
Nashville (USA)
1515 Demonbreun St
Coverage
- Europe
- North America
- Latin America
- Middle East
- South/North Africa
- India
- South East Pacific
Collaborations
SINTESI RESEARCH collaborates with a wide network of qualified partners.- CENTRAL LABORATORIES has efficient collaborations with GLP / GCP approved central labs.
- INVESTIGATOR SITES AND HOSPITALS SR interacts with an extensive network of research centres, we support Sponsors in selecting the best sites for conducting their studies according to their expectations / needs.
- DRUG SUPPLY MANAGEMENT
SR through the collaboration qualified partners, SR can manage:
- Clinical trials logistics
- Customs process management
- Drug production and stock management
- IMAGING CORE LABORATORIES Integrated in the RDC system the Partners provide EEC, ECG, MR and other study specific imaging for direct upload in the data base allowing an easier centralized reading/evaluation.
Partners list
Let's better know our partners■ Sintesi InfoMedica - Communication and Publishing. Multimedia and paper – based special projects, journal, congress report, slide kit, patients record, Clinical case, educational for Patient, web sites.
■ Homemedics - Clinical testing, Market segmentation analysis, Product launch support, Registration of products, Investment opportunities
Meet the team
Paolo De Simoni
Chief Executive Officer & Scientific Director
Rachel Jacob
Chief Operation Officer & Marketing Director
Andrea Demartini
ICT and IT Manager
Parisa Nejat
Q.A. Manager
Alessandra Rimoldi
Business Development Officer
Sue Bhadare
Clinical Operation Expert - USA
Paolo De Simoni
Chief Executive Officer & Scientific Director
Paolo is the founder of Sintesi Research and since 2005 he is responsible for the overall management of the Company and Company’s operations including research and development.
Paolo brings more than 30 years of experience in the pharmaceutical industry and International CROs.
He covered the role of CRA, Project Director, Head of Cl. Opts., managing and coordinating international clinical trials in several therapeutic areas.
As Scientific Director he is still coordinating the Cl. Opts team directly.
Paolo brings more than 30 years of experience in the pharmaceutical industry and International CROs.
He covered the role of CRA, Project Director, Head of Cl. Opts., managing and coordinating international clinical trials in several therapeutic areas.
As Scientific Director he is still coordinating the Cl. Opts team directly.
Rachel Jacob
Chief Operation Officer & Marketing Director
Rachel has a vast experience of Business development and Marketing on a global level.
She is CFO since 2013 and COO since 2018 at Sintesi Research Israel.
Rachel is responsible for designing and implementing business operations as well as establishing policies that promote company culture and vision.
Andrea Demartini
ICT and IT Manager
Andrea is responsible for IT solutions at Sintesi Research S.r.l. since 2016.
He brings more than 20 years of IT experience, covering system management and maintenance, b2b assistance, retail assistance, network management and system building.
Parisa Nejat
Q.A. Manager
Parisa is the quality assurance, with an 8-year experience in leading, coordinating, and monitoring clinical trials, and has been cooperating with Sintesi Research S.r.l. since 2018. She is responsible for implementing and maintaining the quality system, assessing vendors’ qualifications, coordinating the annual training and quality control plan, and acting as an internal reference to staff regarding quality and regulatory issues. During her career, she has worked in different fields, including rheumatology, oncology, hematology, nephrology, phase I-III, and observational studies, according to the demands of the company itself. In this professional phase also, she has been able to oversee a general vision of the development of a drug with relatively connected problems.
Alessandra Rimoldi
Business Development Officer
Alessandra is a business development manager with 15 years of experience in researching solutions and new business opportunities worldwide.
She joined Sintesi Research in 2021 as responsible for creating strategic marketing plans and contacting potential clients in order to get access to new collaborations. She collaborates with cross-functional teams to improve customer service experience and needs. Focused on building strong and dedicated client relationship and partnership, built on trust.
Sue Bhadare
Clinical Operation Expert - USA
Seasoned professional with over 25 years experience in managing and conducting clinical trials with a strong strategic regulatory background. Extensive background in biologics with many successful clinical trials completed and IND submissions and BLA approvals. She worked in Pharma, Biotech Companies and founded a CRO covering key roles in Clinical Operations Dept. Proficient in supporting companies at the FDA with drug development. Indeed, she has extensive experience in designing regulatory and clinical development strategies during early product development to prepare for Pre- IND/IDE meetings. Led and managed multiple successful Pre-IND meetings and End of Phase II Meetings at CBER, as well as IDE meetings at CDRH.
Reviewed Briefing Books and the primary point of contact through the IND/IDE approval process. Ability to manage global or local projects independently, managing vendors, timelines, budgets and CRAs as needed.
Reviewed Briefing Books and the primary point of contact through the IND/IDE approval process. Ability to manage global or local projects independently, managing vendors, timelines, budgets and CRAs as needed.
Our contact
Our helpline is always open to receive any inquiry or feedback.
Please feel free to drop un an email from the form below and we will get back to you as soon as we can.
Italy HQ
Sintesi Research S.r.l
Via delle Stelline, 9
20146 Milano, Italy
Phone +39 02873512
Fax +39 0297374301
p.desimoni@sintesiresearch.com
info@sintesiresearch.com
Israel
Sintesi Research
Azrieli Towers Harokmim
St. 26 Holon (Tel Aviv)
Phone +972.54.973.9994
r.jacob@sintesiresearch.com
Spain
Sintesi Research
Paseo de Maragall, 23
08026 Barcellona, Spagna
Phone +34 647141166
e.lori@sintesiresearch.com
USA
Sintesi Research
1515 Demonbreun St
Nashville
TN 37203
Phone +1 7036267191
s.bhadare@sintesiresearch.com
Sintesi Research S.r.l.
Via delle Stelline 9 – 20146 Milano
P.IVA & C.F. 05059100965
REA: 1793968
Via delle Stelline 9 – 20146 Milano
P.IVA & C.F. 05059100965
REA: 1793968
