The Cromos Pharma is a Clinical Research Organization (CRO) with experience in rare orphan diseases research. We are one of the few CROs with capabilities to conduct clinical trials across all phases. Our team has extensive experience in managing complex studies for rare and ultra-rare disorders. If you are looking for a best partner in the clinical research industry, Cromos Pharma is the right place for you!
What are the areas Clinical Research Organization (CRO) works:
A CRO is a company that provides support to the pharmaceutical and biotechnology industries in the form of research services outsourced on a contract basis. A number of services provided by Cromos Pharma include:
– Pre-clinical development
This is the stage at which new drug candidates are evaluated for safety and efficacy. The goal of pre-clinical development is to determine the safe starting dose (pharmacodynamics) and then to identify any major side effects (pharmacokinetics) of the new drug.
– Clinical development
This is the stage at which new drugs are tested in humans for safety and efficacy.
– Regulatory affairs
A CRO can also provide support in the form of regulatory affairs services. This includes assistance with the preparation and submission of all required documentation to health authorities.
– Drug safety and pharmacovigilance
Cromos Pharma also offers drug safety and pharmacovigilance services. This includes the monitoring of adverse events and the assessment of risk-benefit profiles for new drugs. Our team can help you ensure that your clinical trials are conducted safely and in compliance with all applicable regulations.
Career Prospects in Clinical Research:
The clinical research industry is growing at an astonishing rate and is opening up a wide scope of employment opportunities for trained professionals. If you are looking for a challenging and rewarding career, clinical research is the perfect choice for you. Cromos Pharma can provide you with the skills and knowledge you need to succeed in this exciting industry.
A Clinical Research Associate (CRA) :
A Clinical Research Associate (CRA) is a professional who works within the clinical research industry to monitor and manage clinical trials. Cromos Pharma is looking for talented and ambitious individuals to join our team as CRAs. As a CRA at Cromos Pharma, you will be responsible for ensuring that our clinical trials are conducted in accordance with all applicable
Clinical data management (CDM):
Clinical data management is a critical component of any clinical trial. Cromos Pharma has a team of experienced CDM specialists who can help you ensure that your data is accurate and compliant with all applicable regulations.
Clinical Research Organisation (CRO) :
A CRO landscape is vast; using a CRO’s expertise you can maximize the efficiency of your clinical trials, but only if you choose the right one for the project at hand.
Typically, a CRO will organize and conduct clinical trials to check the test molecule in humans. As independent companies, they offer an objective assessment of a new drug in the clinical setting and since they partner with many companies, typically provide broader experience.