Sponsors &
Contract Research Organizations

Sponsors working for clinicals trials
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At ResearchLink, we take pride in being your dedicated partner in setting up and managing clinical trials. We understand the complexities involved and aim to streamline the process for you. As a single point of contact, we handle all the necessary administration, including obtaining ethics committee approval, negotiating contracts, and managing payment of fees.

We recognize the importance of speed in study setup and patient recruitment. By understanding the unique needs of pharmaceutical researchers and contract research organizations (CROs), we prioritize fast study initiation and accelerated recruitment of eligible patients. Our team of experienced professionals, trained in Good Clinical Practice (GCP), ensures the collection of high-quality data, resulting in fewer queries and improved efficiency.

One of our key objectives is to alleviate the monitoring and management burden on sponsors or CROs. By providing robust support and expertise, we simplify trial supply and documentation processes. This not only saves time but also reduces costs associated with monitoring. Our aim is to create a seamless and efficient experience for all stakeholders involved in clinical trials.

Services

We are committed to supporting the success of your clinical trials by providing comprehensive services that promote transparency, efficiency, and quality.

Feasibility & site identification

Our strong partnership with investigators and a comprehensive database enable us to efficiently assess study feasibility, recommend suitable sites, and facilitate successful collaborations, advancing clinical research progress.

Contract & budget negotiation

ResearchLink simplifies the contract and budget negotiation process by serving as a centralized contact point, streamlining administrative tasks, and ensuring clear communication, allowing researchers to efficiently kickstart their studies.

Subject recruitment

Through our strong partnership with investigators, we leverage a valuable database to assess study feasibility and recommend sites that meet sponsor requirements, facilitating successful collaborations and advancing clinical research progress.

Training

Our priority is to provide extensive training to our investigators, equipping them with the necessary knowledge and skills to conduct clinical trials at the highest standards. Our comprehensive programs cover a wide range of topics, ensuring professionalism, efficiency, and strong relationships with study subjects.

Study coordination

We are your dedicated partner in coordinating and managing clinical trials, handling all administrative tasks and ensuring a smooth process. Our focus is on speed, efficiency, and alleviating the burden on sponsors and CROs. With our expertise, we simplify trial processes, save time, and promote transparency and quality in clinical research.