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April 24, 2013

Biogen Idec, Forest and Bayer Among Top Sponsors Rated by Investigative Sites in New CenterWatch Survey

More than 2,000 global investigative sites rate the best biopharmaceutical companies to work for in a new survey conducted by...
pharmacuetical business review
April 24, 2013

CenterWatch Commemorative April Issue Profiles 20 Innovators Transforming the Clinical Trials Industry

CenterWatch, a leading provider of global clinical trials information, is marking the 20th anniversary of its flagship publication The CenterWatch...
pharmacuetical business review



Since 1994, CenterWatch has been the recognised global leader in providing clinical trials information to a broad and influential spectrum of clinical research professionals ranging from top pharmaceutical companies and CROs to research sites and niche industry providers, as well as an engaged population of patients interested in clinical research and volunteering.

The largest online database of actively recruiting, industry-sponsored clinical trials

cwAs a pioneer in publishing clinical trials information, CenterWatch was the first website to publish detailed information about clinical trials that could be freely accessed by patients and their advocates. Today, we have the largest online database of actively recruiting, industry-sponsored clinical trials.

Products and services

Contact details:

10 Winthrop Square
Fifth Floor
MA 02110
Phone: 617 948-5100
Fax: 617 948-5101

Business Development and Partnership Opportunities

Industry provider profile pages create visibility for contract service providers to showcase their products and services on to the clinical trials community making it a useful and cost-effective way for providers to generate new business leads, increase exposure and reach a captive and targeted audience.

Profile pages are completely customisable and can include images and links to video presentations, demos and company documents.Partnership opportunitiesCenterWatch has developed numerous partnerships and professional relationships with sponsors, CROs, health associations, niche providers and other organisations to better provide the clinical research community and patients with access to the most current and relevant industry, educational…

Clinical Research Career Services

JobWatch is the industry's only online career and educational resource dedicated to clinical research professionals.

Job seekersView and apply for open positions, post your resume and cover letter and find upcoming networking events, training or academic degree programmes for career advancement.EmployersWith thousands of monthly visitors and exclusive outreach efforts to drive traffic directly to online postings, employers have an opportunity to reach a highly targeted and engaged audience via a…

Clinical Research News

Access news and intelligence with CenterWatch's following publications:

The CenterWatch MonthlyThe CenterWatch Monthly is the industry's leading analytical source for business news and information about the clinical trials industry.Each issue covers timely and relevant topics with access to proprietary data and analysis, as well as 25+ clinical study leads and in-depth drug intelligence. This is all included to help you better navigate and…

Clinical Research Training Guides

CenterWatch's training guide series are comprehensive educational resources focused on improving clinical research management skills to conduct safer, more efficient clinical trials.

These guides are perfect for professionals of all skill levels or as a valuable resource for any internal training program or academic curriculum.Becoming a Successful Clinical Research Investigator (print only)The CRA's Guide to Monitoring Clinical Research (print or ebook)The CRC's Guide to Coordinating Clinical Research (print or ebook)Global Issues in Patient Recruitment and Retention (print…

Clinical Study Leads and Site Identification Services

CenterWatch boasts a wide range of clinical study leads and site identification services:

Research center profile pagesResearch center profile pages are an easy and cost-effective way for investigative sites to showcase detailed information on This information can include their site offerings and expertise which will help generate new clinical research study leads, secure contracts, increase the company's exposure, as well as reach out to their target audience.Profile…

Content Licensing

CenterWatch offers licensing of our database-driven and static-text content to provide companies with the latest in scientific clinical trial activity and drug development information using market intelligence and knowledge resources. Content can be offered as data feeds and co-branded to seamlessly integrate with a company's web site or Intranet.

Content LicensingOur offerings include:Clinical Trials Listing Service™Drugs in Clinical Trials DatabaseRecently Approved Drugs by the FDANew Medical Therapies™Patient EducationPublication Content PortalClinical Research Training GuidesContact details:Joan ChambersPhone: 617 948-5100Email:

Market and Drug Intelligence Services

Since 1994, CenterWatch has been a forerunner in tracking, analysing and reporting on the latest trends in the clinical trials industry. Unprecedented business knowledge of the clinical research enterprise, combined with proprietary data and global contacts, gives CenterWatch a unique and objective position in the market to provide invaluable, custom reports for competitive and market analysis.

Custom market intelligence servicesOur comprehensive offerings focus on all aspects of the life sciences and clinical trials industry, including:Secondary data analysisInterviewsFocus group researchCustomer surveys e.g. outsourcing and vendor evaluations; research and examination of new industry technologies; company performance and relationships; post-trial analysis to gauge site success; volatility of global investigative site infrastructure.Contact details (market research):Phone:…

Medical Writing Services

CenterWatch provides comprehensive medical writing and custom publishing services for pharmaceutical, biotech and contract research organisations to support their clinical development initiatives through post-approval marketing.

Medical writing services has expanded offerings and expertise in the healthcare, academia and medical communications sectors.CenterWatch offers medical writing solutions for global regulatory affairs and medical affairs departments to a select group of sponsor and CRO companies. We aim to provide our clients with unmatched expertise, collaborative efficiency, unprecedented quality registration documents and primary manuscripts.Contact…

Patient Education Centerwatch

We make sure volunteers awaiting clinical trial are well-informed and feel at ease, thanks to our useful guides.

Volunteering for a Clinical TrialAn easy-to-read, IRB-approved pamphlet designed as a quick reference guide for potential volunteers interested in participating in a research study. It includes an overview of the clinical trials process and answers some of the most commonly asked questions about volunteering for a clinical trial. Translations available in Spanish, French, Italian, Portuguese,…

Patient Enrollment Services

Patients and volunteers can be enrolled easily and efficiently with CenterWatch's clinical trials listing service.

Clinical Trials Listing Service™CenterWatch's clinical trials listing service is the leading online resource for patients seeking actively recruiting clinical trials, having reached more than 25million potential study volunteers since launching in 1994.Today, with 80,000+ listings and a range of exclusive outreach efforts designed to maximise traffic to your clinical trial listings, CenterWatch continues to be…

Regulatory Compliance

CenterWatch has developed a multitude of procedures to maintain pharmaceutical regulations and guidelines.

Standard operating procedures for the conduct of clinical researchStandard operating procedures for the conduct of clinical research has been created to help clinical research sites maintain rigorous standards in a world of declining resources.The template has been expanded to include more procedures to assess study feasibility, recruit subjects and ensure regulatory compliance. It is based…
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