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About Synergic Clinical Research

Synergic Clinical Research (SCR) is a focused Site and Project Management Organization providing customized solutions to cater unmet need for quality scientific evidence generation to fulfil the requirement of Research and Development for the betterment of Patients.  


SCR has a proven model to provide new efficiencies to clinical trial conduct. Clinical Trial programs utilizing our service with physician, investigative sites are provided with faster patient enrolment, superior data, and an overall faster trial completion than programs utilizing the traditional model.

Trained study coordinators work side by side with the physicians and intuition to ensure all protocol requirements are completed as intended and on time.


SCR has successfully implemented clinical studies since its inception in 2008 in various therapeutic areas like Cardiology, Diabetes, Pulmonology, Orthopaedic, Critical Care, Gynaecology, Nephrology, Neurology, Vaccine, Ophthalmology, Gastroenterology and Rare Indications.

SCR Logo

Patient Safety and Confidentiality is our highest priority and SCR team ensures that all the conditions required for the same is adhered to the highest standard and as mentioned in the Site SOP.

Our services typically include identifying and recruiting suitable clinical trial sites, managing site operations, ensuring adherence to regulatory guidelines, and monitoring the overall progress of studies. SCR strives to streamline the clinical trial process, enhance patient recruitment, and maintain data quality, contributing to the development of new drugs and therapies. Synergic Clinical Research is committed to advancing medical research and improving patient healthcare outcomes.



SCR is committed to work for the benefit of mankind by setting up high standards in delivering solutions for Pharmaceuticals and Healthcare industry to generate and establish scientific evidence.



Ensure that the core principles of research ethics are maintained- 

  • Respect for the persons 

  • Beneficence & non- maleficence

  • Justice

  • Inform Consent 

  • Confidentiality and Data Protection Integrity

  • No Conflict of Interest



  • Feasibility, Site Selection & Onsite Trial Management.

  • Project Management and Monitoring for Phase clinical trials.

  • Patient recruitment & Retention strategies.

  • Regulatory support.

  • Clinical trial staff support.

  • Assessments of sites and investigator qualifications.

  • Training of investigators and their teams (e.g. GCP, safety reporting, IMP handling).

  • Ethics committee and regulatory authority submissions and queries resolution.

  • Investigator Site File compilation and review.

  • Good Clinical Practices (GCP) monitoring.

  • Study logistics support.

  • Responsible for any site audits and inspections.

  • Preparation of investigator meetings.

  • Regular training programs for the Site team members.

  • Internal  Compliance Audit.

  • End to End Clinical Research Services for Investigation and Industry Initiated studies.


Our USP​

  • Ensure correct & documented Informed Consent (ICF) process.

  • Obtaining Ethics committee approvals & timely communication

  • IP Accountability, Storage & Return or disposal of IP

  • Ensure 100% documentation, SD & CRF completion.

  • Ensuring logistics including lab samples and couriers.

  • Scrutinize lab results and update PI.

  • Track, enrollment & Ensure 100% follow up Study site Finances management.

  • Overall study conduct responsibility at site Identify Investigator's network & Initiate cross referrals.

For more information please contact us at

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