About LEADER research

Dr. Lanzini collaborates closely with the research team to ensure that each study is conducted with the highest standards of quality, compliance, and participant care. She plays a key role in assessing participant eligibility, monitoring safety, and ensuring protocol adherence throughout the duration of clinical trials.

With a patient-centered approach, Dr. Lanzini is passionate about fostering trust and communication with participants, ensuring they feel supported and informed during their clinical trial journey. Her expertise in dermatology brings valuable insights to studies focused on skin-related conditions, enhancing the quality and relevance of research outcomes.

As part of LEADER research, Dr. Lanzini is proud to contribute to innovative clinical studies that improve patient care and advance medical science. Her dedication to excellence and her collaborative spirit makes her a vital asset to the LEADER team.

Dr. Woodsford works collaboratively with the principal investigator and research team to oversee participant safety and adherence to regulatory standards. His analytical approach and dedication to ethical research practices are essential in maintaining the integrity and reliability of the trials conducted at LEADER research.

With a deep understanding of clinical trial processes and a passion for innovation, Dr. Woodsford is committed to improving health outcomes through research. He is dedicated to fostering trust and communication with study participants, ensuring they are well-informed and supported throughout their clinical trial journey.

Dr. Woodsford is proud to be part of LEADER research, contributing to its mission of advancing scientific discovery and improving patient care through groundbreaking clinical research.

Before her current role, Vivian gained hands-on research experience as a Sub-Investigator in Brazil, where she collaborated on numerous clinical trials, contributing her medical expertise as a rheumatologist to ensure participant safety and protocol compliance. Upon joining LEADER research, she further honed her skills as a Clinical Research Coordinator, managing day-to-day trial operations, participant engagement, and data collection. These roles provided her with a comprehensive understanding of clinical research processes, from operational logistics to patient-centered care.

Working under the supervision of Dr. Lima, Vivian is integral to advancing LEADER’s mission by building strong relationships with sponsors and partners, facilitating seamless trial operations, and ensuring that study participants remain the central focus of every project.

Vivian’s contributions extend beyond operations; she is actively involved in recruiting and mentoring research staff, ensuring the team is equipped with skilled professionals dedicated to advancing clinical research. Her strategic approach, combined with her medical expertise and operational experience, has been critical to the success of numerous studies conducted in Hamilton, Ontario, and internationally.

Her work exemplifies a commitment to innovation, precision, and participant care, ensuring every trial prioritizes safety, well-being, and access to cutting-edge treatments.

In her role, Roberta manages the day-to-day activities of clinical trials, including participant recruitment, informed consent processes, data collection, and monitoring. Her organizational skills and attention to detail are key to maintaining accurate study documentation and ensuring compliance with Good Clinical Practice (GCP).

Roberta’s ability to build trust and rapport with participants underscores her commitment to patient-centered care, ensuring that every individual feels supported and valued throughout their clinical trial experience. She also works closely with investigators and sponsors to facilitate effective communication and smooth study operations.

As part of the LEADER research team, Roberta is passionate about contributing to advancements in medical science and improving access to innovative treatments for patients. Her dedication and expertise continue to be instrumental in the success of LEADER’s clinical research endeavors.

Sib's expertise in clinical research coordination includes managing study protocols, ensuring compliance with regulatory requirements, and overseeing the smooth operation of clinical trials. Her background in regulatory affairs provides a strong foundation for navigating the complexities of clinical research regulations and guidelines.

Sib is dedicated to maintaining the highest standards of research integrity and patient safety. Her attention to detail and organizational skills contribute to the successful execution of research projects. Sib's commitment to continuous learning and professional development makes her an integral part of the LEADER research team.

Outside of her professional responsibilities, Sib enjoys staying informed about the latest developments in clinical research and regulatory affairs. She is passionate about contributing to advancements in medical research and improving patient outcomes through her work.

In her role, Luisa oversees key trial activities, including participant recruitment, informed consent, data collection, and regulatory compliance. Her meticulous approach ensures that all study protocols are followed and that data is accurate and reliable. Luisa’s ability to manage multiple priorities and maintain clear communication with investigators, sponsors, and participants ensures the smooth progress of each clinical trial.

Known for her compassionate and patient-centered approach, Luisa is dedicated to making study participants feel comfortable, informed, and supported throughout their clinical trial journey. Her commitment to ethical research practices and attention to detail help ensure the highest quality outcomes.

As part of LEADER research, Luisa is proud to contribute to advancing medical innovation and improving access to cutting-edge treatments. Her professionalism and dedication are key to the success of LEADER’s research initiatives.

In her role, Lin manages a range of critical trial activities, including participant recruitment, informed consent processes, and data collection. Her medical background enhances her ability to assess and monitor participants’ health, ensuring their safety and well-being throughout the study. Lin ensures that all study protocols are followed meticulously and that data is collected and documented accurately, maintaining compliance with Good Clinical Practice (GCP) and regulatory requirements.

Lin is committed to fostering strong relationships with study participants, ensuring they feel informed, comfortable, and supported during their clinical trial experience. Her medical expertise and organizational skills contribute to the integrity and success of each trial.

As part of LEADER research, Lin is dedicated to advancing medical science and improving patient outcomes through the efficient and ethical conduct of clinical research. Her dedication, professionalism, and medical knowledge are key to the success of LEADER’s research initiatives.

As a rheumatologist, Jamela brings a specialized understanding of complex medical conditions, which enhances her ability to monitor participant health and ensure safety throughout the study process. At LEADER research, she oversees key trial activities, including participant recruitment, informed consent, data collection, and regulatory compliance. Her ability to integrate medical knowledge with research operations ensures accurate and reliable trial outcomes.

Jamela is deeply committed to patient-centered care, fostering trust and communication with participants to ensure they feel valued and supported during their clinical trial journey. Her collaborative approach and attention to detail make her an essential part of the LEADER research team.

Passionate about advancing medical innovation, Jamela contributes to LEADER’s mission of delivering impactful clinical research and improving access to groundbreaking treatments. Her unique combination of medical expertise and research skills is vital to the success of LEADER’s studies.

At LEADER research, Yessica is responsible for overseeing the laboratory’s daily operations, including specimen handling, processing, and ensuring compliance with Good Clinical Laboratory Practice (GCLP) standards. Her meticulous attention to detail ensures the integrity and reliability of lab data, which is critical to the success of clinical trials.

Yessica works closely with the research team to provide seamless support for clinical studies, assisting with data collection, sample management, and ensuring that all laboratory procedures align with protocol requirements. Her expertise as an MLT enhances LEADER’s ability to deliver high-quality research outcomes while maintaining participant safety and well-being.

Passionate about advancing clinical science, Yessica is privileged to contribute to LEADER research’s mission of improving patient care through innovative treatments and rigorous research. Her professionalism, technical skills, and dedication to excellence make her an invaluable member of the LEADER team.

Currently, Diana focuses on supporting clinical trials by managing key technical processes, including electronic Patient-Reported Outcomes (ePROs), medical imaging (e.g., photos), electrocardiograms (ECGs), and other study-related assessments. Her attention to detail and proficiency with specialized equipment ensure the collection of accurate and reliable data, critical to the success of every trial.

With her laboratory background, Diana is adept at ensuring compliance with rigorous clinical and regulatory standards. She works closely with investigators and the research team to provide seamless operational support, ensuring that each trial runs efficiently and prioritizes participant care.

Diana is deeply committed to advancing medical innovation through clinical research. Her technical skills, dedication to precision, and passion for improving health outcomes make her an invaluable member of the LEADER research team.

At LEADER research, Estella is primarily focused on participant recruitment, leveraging her strong interpersonal skills and attention to detail to engage with potential participants and guide them through the clinical trial process. Additionally, as a float team member, Estella is adept at adapting to any trial-related task, providing seamless support wherever it is needed to ensure the smooth operation of studies.

Estella’s background as an MLT enhances her ability to approach clinical research with precision and a deep understanding of scientific protocols. Her flexibility, problem-solving skills, and dedication to participant care make her an invaluable asset to the team.

Committed to advancing medical research and improving patient outcomes, Estella is delighted to contribute to LEADER research’s mission of conducting high-quality, impactful clinical trials. Her adaptability, professionalism, and enthusiasm for research make her a key part of LEADER’s success.

Tosin's current focus includes trials data entry, blood and vital signs collection, and other administrative research tasks. Her meticulous attention to detail and commitment to excellence ensure the accuracy and reliability of research data. Tosin's passion for biochemistry and clinical research drives her to continually enhance her skills and knowledge, making her a valuable asset to the LEADER research team.

In addition to her technical skills, Tosin is known for her collaborative spirit and ability to work effectively within multidisciplinary teams. She is dedicated to advancing the field of clinical research and improving patient outcomes through her diligent work. Outside of her professional life, Tosin enjoys staying updated with the latest advancements in health science and spending quality time with her family.

Currently, Joy specializes in managing clinical trial pharmacy tasks, including investigational product handling, inventory management, and compliance with regulatory and protocol-specific requirements. Her attention to detail and commitment to precision ensure the accurate execution of pharmacy-related responsibilities. In addition, Joy is proficient in performing other essential tasks as needed, making her a flexible and dependable member of the research team.

Joy’s combined experience in nursing and laboratory science allows her to approach her role with a comprehensive understanding of patient care and clinical operations. Her ability to adapt to various responsibilities and her dedication to maintaining high standards make her an invaluable asset to LEADER research.

Passionate about advancing clinical research, Joy is committed to contributing to LEADER’s mission of improving patient care through innovative and high-quality clinical trials. Her professionalism, versatility, and dedication to excellence continue to drive the success of LEADER’s research initiatives.