Clinical Research Job Training
There has never been a better time to enter research. As the number of clinical trials continues to rise, so does the demand for qualified research professionals to conduct the trials effectively and efficiently.
Why become a Clinical Researcher?
- High Demand: A job search for clinical research on LinkedIn in the United States lands over 68,000 available positions as of September 2021
- Trials: A quick trial search of clinical trials on clinicaltrials.gov reveals over 145,000 trials in the United States as of September 2021.
Be job-ready in 12 weeks
- Learn day-to-day job skills and activities as a clinical research professional.
- Career Coaching + Resume Building + Cover Letter + Interview Preparation + Networking Support.
Why choose NLCR?
- An effective, engaging, interactive, and self-paced learning experience that fits in with most types of learners.
- Interact with highly qualified instructors, Research Coordinators, and Principal Investigators.
- A more pragmatic approach helps to develop and master fundamental skills in less time.
- Oncology research special sessions.
- Externship (Optional).
- Affordable fee compared to others available in the market.
ADMISSION REQUIREMENTS
Trainees must be at least 21 years of age with at least two years of college credit and some medical/healthcare background. To enroll, click here.
Our Instructors
EKTA GREWAL, M.Sc. (Lead instructor)
Ekta started her career as a researcher at university and later pursued her career as a lead coordinator and development specialist at multiple sites working in collaboration with world-renowned Sponsors/CROs. Over the years she has worked in different capacities, including building study pipelines for the sites, boosting patient enrollment through refined strategies, and managing day-to-day operations of clinical trials. She has significant exposure to several aspects of clinical trials, including supporting physicians to build research arms in their practice, training research coordinators, recruiting research staff, cross-functional research knowledge, and execution success. Her years of experience and expertise led to the formation of NLCR. She is very passionate about research and her goal is to excel and help others excel in research.
NIRAJ PATEL, MS
Niraj is an experienced Oncology Research Professional with an amazing background in working in the research industry. He is skilled in Medical drugs and Devices, Clinical TrialOperations, Biotechnology, and Healthcare. He is a strong business development professional with an education background focused on Clinical Research Administration from Johns Hopkins. He founded PRiSMS Group and works with community hospitals in the development of clinical trial programs. He is an irreplaceable asset for NLCR as an Instructor for the Clinical Research Training program; passionate about sharing his decades of research knowledge and insights with new trainees.Guest Speakers
Susan Kesler, RN
Susan Kesler, RN has decades of clinical research experience in phase II-IV trials. She has been working as a Research Nurse at a busy site Dayton Gastroenterology, Inc. in Ohio, the largest gastroenterology practice in the area focused on providing treatment for digestive disorders in the digestive tract, which includes the esophagus, stomach, small intestine, and colon. Her strengths include supporting the day-to-day operations at the site, patient care, new staff training, ensuring enrollment success, and adherence to SOPs and industry guidelines. She is a very proactive and charming personality with extensive knowledge of ICH/GCP guidelines, QA processes, and regulatory standards. She has been a speaker at research conferences and will serve as a Guest Speaker in the clinical research training program at New Life Clinical Research.
Aman Khera
Aman Khera, a global regulatory affairs leader, and strategist has 25 years of experience in the clinical research industry. She is a recognized expert, providing global strategic direction in regulatory affairs. She has led a wide variety of regulatory projects providing regulatory strategy and development services in many therapeutic indications. She is passionate about helping sponsors develop comprehensive regulatory strategies and has worked with a number of agencies across the world. She is well respected and recognized for her track record in anticipating and addressing inevitable regulatory challenges in the development journey. Her insight has changed the way people think about regulatory affairs and has resulted in fewer late-stage surprises, smoother trials, and optimal outcomes for the development of new therapies. She is committed to diversity and inclusion in clinical research and advises in the industry on how best to action into practical strategies. She serves on the emTRUTH advisory board, bringing a unique perspective on how regulations, ethics, and compliance interplay within blockchain for healthcare. She is also a 2021 PharmaVOICE 100 honoree, recognized as one of the most influential and inspiring people in the life sciences industry. She volunteers her time with organizations such as DIA, The Organization for Professionals in Regulatory Affairs (TOPRA), and the Regulatory Affairs Professionals Society (RAPS) as well as Sikhs in Clinical Research.Student Testimonials
Public Opinion
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