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Open to workDesired start date: Immediately
Open To Work
Esther Titus, MD, MHA
Clinical Research Professional
Queens,NY
Work Preference
Summary
Senior Clinical Research Associate with MD and MHA, possessing over 7 years of experience in leading oncology and multi-therapeutic trials from Phases I to IV. Demonstrated success in collaborating with investigators and site teams to enhance patient enrollment and ensure strict protocol compliance, resulting in audit-ready outcomes. Expertise in clinical data analysis and effective communication of scientific findings to healthcare professionals. Seeking to transition into a Medical Science Liaison role to utilize clinical knowledge and field experience in engaging key opinion leaders and advancing cancer therapies.
Overview
15
15
years of professional experience
1
1
Certification
Work History
Senior Clinical Research Associate II
IQVIA
Parsippany, New Jersey
03.2024 - 12.2024
- Led monitoring across 15+ oncology sites (PSV, SIV, IMV, COV), ensuring 100% compliance with ICH, GCP, and FDA standards.
- Partnered with investigators and coordinators to optimize enrollment timelines, reducing ramp-up by 28%.
- Facilitated biomarker and PK workflow training, strengthening protocol adherence, and trial documentation.
- Mentored new CRAs, reinforcing best practices, and global monitoring consistency.
Senior Clinical Research Associate I
Syneos Health
Morrisville, North Carolina
10.2022 - 09.2023
- Oversaw global respiratory oncology trials, cutting protocol deviations by 12% through proactive site engagement.
- Boosted patient enrollment by 35% with targeted feasibility analyses and site-specific strategies.
- Built a GCP-compliant performance dashboard for early detection of trial risks.
- Trained site managers and CTAs, strengthening compliance and team capability.
Clinical Research Associate II
ICON plc
Blue Bell, Pennsylvania
09.2021 - 09.2022
- Managed Phase I–III studies, improving startup forecasting accuracy by 37%.
- Delivered feasibility assessments and enrollment strategies that enhanced trial outcomes.
- Supported SOP development and global training initiatives.
- Conducted data analysis to identify trends for decision-making.
Clinical Research Associate I
PolyCRA (formerly TPKR)
San Antonio, Texas
04.2019 - 09.2021
- Standardized monitoring templates, reducing qualification time by 22%.
- Developed site risk dashboards to track deviations and improve recruitment oversight.
- Coordinated multi-site trials, achieving zero audit findings.
- Authored training materials, boosting onboarding efficiency for study teams.
Clinical Research Coordinator – Oncology
First Family Care Private Clinic
Brooklyn, New York
09.2018 - 04.2019
- Coordinated oncology trial startup and informed consent, improving patient follow-up by 30%.
- Enhanced data collection methods, reducing administrative burden, and accelerating reporting timelines.
- Collaborated with investigators to refine eligibility criteria, increasing recruitment quality.
Resident Medical Officer /Resident Physician
Indian Private Hospital
Nagpur, Maharashtra (INDIA)
10.2009 - 07.2016
- Delivered direct patient care, improving recovery outcomes through evidence-based protocols.
- Conducted audits to identify and implement safety and treatment improvements.
- Implemented digital medical records, reducing administrative workload, and improving accessibility.
- Guided multidisciplinary teams, fostering collaboration, and patient-centered care.
Education
Adavnced Drug Safety & Pharmacovigilance - Pharmacology And Toxicology
Sollers College
New Jersey11-2018
Master of Science - Health Care Administration & Management
Datta Meghe Institute Of Medical Sciences
Wardha (Maharashtra) INDIA06-2015
M.D. - General Medicine
Kazan State Medical University
Kazan, (Tatarstan) RUSSIA07-2009
Skills
- Clinical monitoring
- Data management
- Regulatory compliance
- Trial design
- Safety reporting
- Patient recruitment
- Oncology clinical trials
- Site and investigator engagement
- KOL collaboration
- Data analysis
- Scientific communication
- ICH GCP
- FDA guidelines
- TMF compliance
- Feasibility and enrollment strategies
- Training and mentorship
Therapeutic Expertise
• Oncology (6+ yrs): Breast (HER2+, Phase III, 4 yrs), Ovarian (Phase III, 3 yrs), GI/Colorectal, BTC & Head & Neck (Phase III,
• Women’s Health (2 yrs): Hormonal & reproductive health, ovarian/breast overlap
• Hematology (2 yrs): ALL, AML, CLL (Phase II–III)
• Neurology (1 yr): Migraine (Phase IV, 1 yr)
• Autoimmune (1 yr): Systemic Lupus Erythematosus (Phase II)
Certification
- Advanced Drug Safety & Pharmacovigilance: Sollers, College, NJ
• GCP Certification: NIDA Clinical Trial Network
• IATA Certification: Mayo Clinic, ASCLS PACE Certified
Accomplishments
- Syneos Health Recognition: Achieving database lock for study DS1062A-U301
- Recognized for 100% audit readiness and flawless TMF compliance during sponsor and regulatory inspections
Affiliations
Completed Project (MHA)| Wockhadt Hospital | Got Approved | Jan 2015 - Apr 2015 |Cost Cutting Ideas in replacement of Crepe Paper with Reusable Green Linen in packaging of Surgical Instruments.
Languages
Spanish
Professional
Hindi
Professional
Russian
Professional
Marathi
Professional
Punjabi
Professional
Work Authorization
- Authorized to work for any US, employer without sponsorship
References
References available upon request.
Timeline
Senior Clinical Research Associate II
IQVIA
03.2024 - 12.2024
Senior Clinical Research Associate I
Syneos Health
10.2022 - 09.2023
Clinical Research Associate II
ICON plc
09.2021 - 09.2022
Clinical Research Associate I
PolyCRA (formerly TPKR)
04.2019 - 09.2021
Clinical Research Coordinator – Oncology
First Family Care Private Clinic
09.2018 - 04.2019
Resident Medical Officer /Resident Physician
Indian Private Hospital
10.2009 - 07.2016
Adavnced Drug Safety & Pharmacovigilance - Pharmacology And Toxicology
Sollers College
Master of Science - Health Care Administration & Management
Datta Meghe Institute Of Medical Sciences
M.D. - General Medicine
Kazan State Medical University
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