CLINICAL RESEARCH:
MEDICAL MONITORING/ CLINICAL DEVELOPMENT LEADERSHIP
The clinical research process relies on the expertise of a physician (medical monitor or clinical lead) to oversee the GCP and safety aspects in a clinical trial. Medical monitors ensure the safety and integrity of the trial subjects throughout the trial, from the initial design of the study to the final close out and CSR completion.
A medical monitor acts as the point of reference for study team members and investigative sites and determines how to evaluate safety events within a clinical trial.
WHO WE ARE
CureEon has extensive Clinical Research experience in a number of different therapeutic areas, including Autoimmune disorders (amyloidosis, UC, Crohn's disease, IBD, angioedema, RA, GvHD, psoriasis, etc.), oncology/immuno oncology (both solid tumor and hematologic malignancies), CNS (Parkinson's disease, epilepsy, multiple sclerosis, anxiety, depression, schizophrenia, ADHD, dementia, nerve agent antidotes, etc.), hematology (anemia, thrombocytopenia, etc.), gene therapy (multiple rare diseases), cardiovascular (hypertension, MI, stroke, etc.), pulmonary medicine (high frequency ventilation, IPP, etc.), ID (COVID-19, hepatitis, fungal, HIV, etc.), vaccines (including COVID-19, pneumococcal conjugate and oncology vaccines), pain management (including Schedule I through Schedule V), metabolic disorders, musculoskeletal (including osteoporosis, wound healing, tissue transplantation), renal medicine and endocrinology.
/CLINICAL RESEARCH EXPERIENCE
/PROCESS
CLINICAL SUPPORT DURING THE CLINICAL RESEARCH PROCESS
From the outset of a clinical trial, the medical monitor plays a crucial role in its development. Medical monitors provide input on the protocol design and create the medical monitoring plan utilized for safety procedures throughout the trial.
In addition to the training of the projects team on the trials protocol inclusion and exclusion criteria, they also work with investigators, site staff, and clinical teams to assist with questions on concomitant medications, medical conditions, and prohibited drugs.
A knowledgeable medical monitor efficiently expedites the process of starting up a clinical trial. Utilizing a clinical research physician with expertise in placing the correct medical monitor on a study and offering guidance sets trials up for successful completion from the start.
MEDICAL MONITORING AND SAFETY STEWARDSHIP
Medical monitors provide round the clock emergency coverage on all safety related matters. If an adverse event occurs, medical monitors determine how to code those events and work closely with the principal investigator whether unblinding is required.
It's the medical monitor's responsibility to review all safety related data to track participants' health and monitor for any potential issues.
Medical monitors work under the expectation that they are part of the core clinical project team. Typically, they attend investigator meetings, project team and sponsor meetings and keep themselves available for questions and concerns.
/MEDICAL MONITORS IN CLINICAL TRIALS
WHO WE ARE
/RANGE OF SERVICES
At CureEon, we offer a wide range of services to support your clinical research efforts. Our expertise includes, but is not limited to:
STUDY
DESIGN
We collaborate with you to design clinical trials that meet regulatory requirements and deliver meaningful results. Our team of experts ensures that your study is well planned and executed.
PATIENT RECRUITMENT
We understand the importance of recruiting the right participants for your clinical trials. Our strategies help you find the right subjects, ensuring the success of your study
CLINICAL TRIAL MONITORING
We provide ongoing monitoring and oversight to ensure your clinical trials progress as planned, identifying and addressing any issues that may arise.
REPORTING AND ANALYSIS
We assist in the preparation of comprehensive reports and analyses of your clinical research data. Our reports are designed to meet regulatory requirements and help you make informed decisions.
WHY CHOOSE CUREEON FOR CLINICAL RESEARCH:
What sets CureEon apart from the competition is our commitment to excellence. Our team comprises seasoned professionals with a wealth of experience in clinical research. We have a proven track record of successful engagements in the field. When you choose us, you benefit from:
Expertise: Our team's deep knowledge and experience in clinical research ensure the highest quality results.
Efficiency: We streamline the clinical research process to save you time and resources.
Dedication: We are committed to the success of your research project, delivering results on time and within budget.
/WHY CHOOSE US
CONTACT US
If you are ready to take your clinical research to the next level, we invite you to get in touch with CureEon.
