Explore Clinical Trials Sites in Plano and Dallas
At AIM Trials, our dedicated team of experienced physicians and research professionals is committed to providing top-tier care for participants and dependable support for study sponsors. As one of the leading Clinical Trials Sites in Plano and Clinical Trials Sites in Dallas, we focus on advancing health and wellness through innovative, patient-centered clinical research for adults and children.
Leading Clinical Trial Sites for Research in Plano & Dallas
AIM Trials plays a vital role in conducting research across multiple therapeutic areas, evaluating the effectiveness and safety of new medications and treatments. Recognized among top Clinical Trials Sites in Dallas and Clinical Trials Sites in Plano, our studies span internal medicine, dermatology, cardiology, immunology, neurology, OB-GYN, psychiatry (pediatric through adult), oncology, pediatrics, and vaccines—serving diverse medical needs within our community.
We also specialize in human factor and user experience (UX) research, integrating modern technology for decentralized trials that combine remote participation with in-person or hybrid visits. This model supports broader accessibility and convenience for study participants.
The unique design element in our logo—the dot on the “i” in AIM and its continuation throughout our site—symbolizes the clinical trial journey: from discovery and development to delivering solutions that can change lives. Whether you’re seeking care or contributing to global health advancements, AIM Trials stands as a trusted partner among Clinical Trials Sites in Plano and Clinical Trials Sites in Dallas.
Types of Studies
Children/Pediatric
Pediatric Autism
Psychedelic Studies
Treatment-Resistant Depression (TRD)
Our Expertise
Why Choose AIM Trials for
Clinical Research in Plano?
Our Experience
AIM Trials is an experienced group of doctors and medical providers conducting mental and physical health research studies in pediatric and adult populations since 2004. Although we conduct a broad range of studies, we are considered a leader in mental health trials in DFW.
Patient-Centric
Philosophy
Everything we do is based on the welfare of our patients. We empathize with our patients and their families by proactively learning about their desires and needs. Our compassionate staff provides personalized treatment wherever possible throughout the entire study process.
Our People
Our patient-centric focus emanates from our team at AIM. Our founder has worked tirelessly to shatter the mental health stigma within our communities. This passion is embodied by our staff to provide an empathetic and caring approach within our medical research practice.
Our People
As the Founder and CEO of Aim Trials, Sonia has over 18 years of experience in clinical research, project management, and regulatory compliance in both drug and medical device trials. Sonia leads a team of research professionals who are dedicated to delivering high-quality, ethical, and innovative clinical studies in various therapeutic areas for both Pediatric and Adult Populations, with a focus on mental health.
Her mission is to shatter the mental health stigma within the community. Sonia works closely with mental health organizations such as NAMI, Changes, and NOCD.
Driven by a profound commitment to the well-being of our community, Sonia has cultivated a visionary approach that encompasses a multi-specialty site integrated within a private practice. This unique synergy empowers our team of experienced investigators to lead with unmatched expertise in conducting Phase I-IV research trials.
Her aim is to provide exceptional service and value to our clients, partners, and patients, by leveraging her expertise in clinical research design, execution, and reporting, as well as my knowledge of the latest industry standards and best practices.
Sameer Meharunkar leads growth strategies at Aim Trials in Dallas-Fort Worth. With over 22 years of leadership experience in digital transformation and customer experience, he excels in healthcare and clinical trial management. At Aim Trials, he is responsible for strategic partnerships with sponsors, CROs, Site Networks and technology vendors to accelerate clinical study growth.
He advances clinical research through innovative technology adoption and streamlined trial management. His strategic focus includes expanding decentralized clinical trials components, enhancing patient recruitment, and implementing digital health solutions. Sameer actively monitors clinical research technology trends to improve trial efficiency and patient engagement. He manages digital marketing for patient recruitment and oversees financial & clinical trials budget operations to ensure operational excellence.
.
Board Certified in Psychiatry
Dr. Kalra brings over 35 years of clinical psychiatry experience to AIM Trials, with a career spanning inpatient crisis stabilization, hospital-based psychiatric care, and private practice across the Dallas-Fort Worth metro. He completed his psychiatry residency at the University of Texas Health Science Center in Houston and has held staff roles at major regional institutions including Methodist Hospital Richardson and United Behavioral Health Hospital.
After three decades in active clinical practice, Dr. Kalra transitioned fully to clinical research, a deliberate shift that gives AIM Trials a PI whose entire focus is study oversight and participant care.
His research experience covers a broad CNS portfolio: MDD, Bipolar Disorder, TRD, PTSD, GAD, Schizophrenia, Alzheimer’s Disease, ADHD, OCD, BPD, and Postpartum Depression.
Peter is a licensed Psychologist in the State of Texas with over 20 years of clinical experience and over 5 years of experience in Clinical Research as a Sub-I/Rater. He has experience conducting rating scales in both Pediatric/Adolescent and Adult Trials in different indications.
Peter has a strong focus on both Adolescent and Adult treatment. He also has lengthy experience working with depression, anxiety, low self-esteem, and other mood disorders. Peter places a lot of attention on issues of diversity (racial, sexual, and gender) and works to provide an environment where one can feel heard and understood.
Lastly, Peter has extensively worked with creative personality types such as artists and musicians and works closely with the area arts community.
Crystal Salas is a board-certified Psychiatric Mental Health Nurse Practitioner and U.S. Army Veteran. With a nursing career spanning since 2010, she brings diverse experience from various healthcare settings, including:
- ICU/Neonatal ICU
- Pediatric Home Health
- Neurology
- Inpatient Treatment/Chemical Dependency
- Utilization Management
Crystal’s professional interests focus on:
- PTSD
- Trauma
- Addiction
- Psychedelic Research
She has furthered her expertise through specialized training with MAPS (Multidisciplinary Association for Psychedelic Studies) and Beckley Academy in psychedelic treatments.
Committed to community service , Crystal volunteers weekly with organizations involved in psychedelic harm reduction, advocates for innovative PTSD/Trauma treatments for veterans and participates in the military peer veteran network, connecting veterans with psychological and community resources.
Crystal’s unique blend of clinical experience, specialized training, and dedication to veteran support makes her a valuable addition to the Aim Trials team.
Sandra brings 30 years of clinical research experience to AIM Trials, where she leads quality assurance across all active studies. Her career spans oncology, dermatology, cardiology, psychiatry, pediatric epidemiology, pulmonology, rheumatology, infectious disease, and vaccine research studies — with roles at institutions including St. Jude Children’s Research Hospital, The Heart Hospital Baylor Plano, and Metroplex Clinical Research Center. She has experience in all aspects of clinical trials at the site level. This includes regulatory, contracts & budgets, study start-up, coordinator tasks and study close-outs. She holds a Bachelor of Science in Psychology from Northwestern State University. Sandra’s depth of experience across therapeutic areas and research settings ensures AIM Trials maintains the highest standards of data integrity and regulatory compliance.
Clinical research professional with over a decade of experience in the health and life sciences industry. With a background in Biotechnology Engineering and a Master’s degree in Clinical Research, I bring strong expertise in regulatory processes and study start-up activities within highly regulated environments.
My experience spans multiple clinical trials, with a focus on regulatory submissions, essential document management, site activation, and cross-functional coordination. I am well-versed in ensuring compliance with ICH-GCP guidelines, maintaining audit-ready documentation, and supporting efficient study initiation timelines.
Known for my attention to detail, organization, and ethical approach, I am committed to maintaining the highest standards of quality and participant safety. I am passionate about advancing clinical research and continuously expanding my knowledge in regulatory affairs and study start-up operations.
Tatyana joined AIM Trials as a recruiter and lab lead, quickly establishing herself as someone who connects with patients and processes equally well. A certified phlebotomist, she has since grown into a Clinical Research Coordinator role — a progression that reflects both her drive and the breadth of skills she brings to the team. Tatyana is deeply motivated by the idea that clinical research gives people a direct hand in their own health outcomes. She plays a central role in the day-to-day execution of our studies from guiding participants through the informed consent process to managing protocol visits, coordinating with sponsors, and ensuring data accuracy across every touchpoint.
Aditi Diggikar has graduated from the University of North Texas with a Bachelor of Arts in Psychology. Aditi joined AIM Trials in 2023; however, she has quickly become an integral part of the operations team.
Clarissa is often the first point of contact for participants at AIM Trials — and the person quietly keeping things moving behind the scenes. She supports study operations across multiple functions, from CRIO data entry and patient pre-screening to scheduling visits and coordinating medical records review ahead of appointments. Her ability to bridge recruitment, clinical operations, and quality assurance ensures that nothing falls through the cracks between a patient’s first call and their first visit. Clarissa’s attention to detail and organizational instincts help our coordinators and QA team stay focused on what they do best.
As the Founder and CEO of Aim Trials, Sonia has over 18 years of experience in clinical research, project management, and regulatory compliance in both drug and medical device trials. Sonia leads a team of research professionals who are dedicated to delivering high-quality, ethical, and innovative clinical studies in various therapeutic areas for both Pediatric and Adult Populations, with a focus on mental health.
Her mission is to shatter the mental health stigma within the community. Sonia works closely with mental health organizations such as NAMI, Changes, and NOCD.
Driven by a profound commitment to the well-being of our community, Sonia has cultivated a visionary approach that encompasses a multi-specialty site integrated within a private practice. This unique synergy empowers our team of experienced investigators to lead with unmatched expertise in conducting Phase I-IV research trials.
Her aim is to provide exceptional service and value to our clients, partners, and patients, by leveraging her expertise in clinical research design, execution, and reporting, as well as my knowledge of the latest industry standards and best practices.
Sameer Meharunkar leads growth strategies at Aim Trials in Dallas-Fort Worth. With over 22 years of leadership experience in digital transformation and customer experience, he excels in healthcare and clinical trial management. At Aim Trials, he is responsible for strategic partnerships with sponsors, CROs, Site Networks and technology vendors to accelerate clinical study growth.
He advances clinical research through innovative technology adoption and streamlined trial management. His strategic focus includes expanding decentralized clinical trials components, enhancing patient recruitment, and implementing digital health solutions. Sameer actively monitors clinical research technology trends to improve trial efficiency and patient engagement. He manages digital marketing for patient recruitment and oversees financial & clinical trials budget operations to ensure operational excellence.
.
Board Certified in Psychiatry
Dr. Kalra brings over 35 years of clinical psychiatry experience to AIM Trials, with a career spanning inpatient crisis stabilization, hospital-based psychiatric care, and private practice across the Dallas-Fort Worth metro. He completed his psychiatry residency at the University of Texas Health Science Center in Houston and has held staff roles at major regional institutions including Methodist Hospital Richardson and United Behavioral Health Hospital.
After three decades in active clinical practice, Dr. Kalra transitioned fully to clinical research, a deliberate shift that gives AIM Trials a PI whose entire focus is study oversight and participant care.
His research experience covers a broad CNS portfolio: MDD, Bipolar Disorder, TRD, PTSD, GAD, Schizophrenia, Alzheimer’s Disease, ADHD, OCD, BPD, and Postpartum Depression.
Peter is a licensed Psychologist in the State of Texas with over 20 years of clinical experience and over 5 years of experience in Clinical Research as a Sub-I/Rater. He has experience conducting rating scales in both Pediatric/Adolescent and Adult Trials in different indications.
Peter has a strong focus on both Adolescent and Adult treatment. He also has lengthy experience working with depression, anxiety, low self-esteem, and other mood disorders. Peter places a lot of attention on issues of diversity (racial, sexual, and gender) and works to provide an environment where one can feel heard and understood.
Lastly, Peter has extensively worked with creative personality types such as artists and musicians and works closely with the area arts community.
Crystal Salas is a board-certified Psychiatric Mental Health Nurse Practitioner and U.S. Army Veteran. With a nursing career spanning since 2010, she brings diverse experience from various healthcare settings, including:
- ICU/Neonatal ICU
- Pediatric Home Health
- Neurology
- Inpatient Treatment/Chemical Dependency
- Utilization Management
Crystal’s professional interests focus on:
- PTSD
- Trauma
- Addiction
- Psychedelic Research
She has furthered her expertise through specialized training with MAPS (Multidisciplinary Association for Psychedelic Studies) and Beckley Academy in psychedelic treatments.
Committed to community service , Crystal volunteers weekly with organizations involved in psychedelic harm reduction, advocates for innovative PTSD/Trauma treatments for veterans and participates in the military peer veteran network, connecting veterans with psychological and community resources.
Crystal’s unique blend of clinical experience, specialized training, and dedication to veteran support makes her a valuable addition to the Aim Trials team.
Sandra brings 30 years of clinical research experience to AIM Trials, where she leads quality assurance across all active studies. Her career spans oncology, dermatology, cardiology, psychiatry, pediatric epidemiology, pulmonology, rheumatology, infectious disease, and vaccine research studies — with roles at institutions including St. Jude Children’s Research Hospital, The Heart Hospital Baylor Plano, and Metroplex Clinical Research Center. She has experience in all aspects of clinical trials at the site level. This includes regulatory, contracts & budgets, study start-up, coordinator tasks and study close-outs. She holds a Bachelor of Science in Psychology from Northwestern State University. Sandra’s depth of experience across therapeutic areas and research settings ensures AIM Trials maintains the highest standards of data integrity and regulatory compliance.
Clinical research professional with over a decade of experience in the health and life sciences industry. With a background in Biotechnology Engineering and a Master’s degree in Clinical Research, I bring strong expertise in regulatory processes and study start-up activities within highly regulated environments.
My experience spans multiple clinical trials, with a focus on regulatory submissions, essential document management, site activation, and cross-functional coordination. I am well-versed in ensuring compliance with ICH-GCP guidelines, maintaining audit-ready documentation, and supporting efficient study initiation timelines.
Known for my attention to detail, organization, and ethical approach, I am committed to maintaining the highest standards of quality and participant safety. I am passionate about advancing clinical research and continuously expanding my knowledge in regulatory affairs and study start-up operations.
Tatyana joined AIM Trials as a recruiter and lab lead, quickly establishing herself as someone who connects with patients and processes equally well. A certified phlebotomist, she has since grown into a Clinical Research Coordinator role — a progression that reflects both her drive and the breadth of skills she brings to the team. Tatyana is deeply motivated by the idea that clinical research gives people a direct hand in their own health outcomes. She plays a central role in the day-to-day execution of our studies from guiding participants through the informed consent process to managing protocol visits, coordinating with sponsors, and ensuring data accuracy across every touchpoint.
Aditi Diggikar has graduated from the University of North Texas with a Bachelor of Arts in Psychology. Aditi joined AIM Trials in 2023; however, she has quickly become an integral part of the operations team.
Clarissa is often the first point of contact for participants at AIM Trials — and the person quietly keeping things moving behind the scenes. She supports study operations across multiple functions, from CRIO data entry and patient pre-screening to scheduling visits and coordinating medical records review ahead of appointments. Her ability to bridge recruitment, clinical operations, and quality assurance ensures that nothing falls through the cracks between a patient’s first call and their first visit. Clarissa’s attention to detail and organizational instincts help our coordinators and QA team stay focused on what they do best.