SIARAM Clinical Research (SCR) offers a wide array of clinical trial and site management services to assist pharmaceutical, biotechnology and medical device companies to bring new drugs and devices to market faster. We are dedicating to provide quality services to connect Sponsors and CROs with trained Investigators. SCR participate in every phase of clinical trial; end-to-end delivery of the complete clinical trial from feasibility to study close out.

Our young and unique team commits to meet the specific requirements of our clients and provide them systematic and reliable data on time.

SCR coordinate clinical trials under strict Global and local regulatory guidelines.

SCR Core Values:

SCR emphasizes on a long term business association through commitment on:

S-Strategic partnership
C-Customer services/satisfaction
R-Reliable for quality, time and integrity

Our Goals

  • Deploying best-in-class clinical research site solutions that help speed up site identification, qualification, initiation, recruitment, retention, budget /contractual negotiations and start up Clinical Trial Processes.

  • To provide faster, predictable, auditable and ethical data of clinical trial patients

  • To provide quality service, responsiveness, and results to our customers striving to be the finest resource & meeting their specific and unique needs.


Management Team

One of the most crucial aspects to delivering a successful project is the quality of the relationship with clients. The Management Team of SIARAM Clinical Research having extensive experience in managing single centric or multi-centric global clinical trial projects, in a number of therapeutic areas. SCR team project and QA managers and Clinical Research Associates (CRAs) are dedicated, qualified and experienced with excellent scientific/medical background and having in-depth knowledge of clinical trial regulations and ICH GCP guidelines.

SCR management team is focused on creating an organization based on quality, credibility, values and ethics.