Houston, TX ***** 361-***-**** adz9fv@r.postjobfree.com

CRYSTAL N MATAKATLA

PROFESSIONAL SUMMARY:

● I am an organized and driven individual, with a clear desire to obtain professional development.

● Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures, and general trial oversight. Excellent problem-solving abilities with a detail- oriented nature. Ready to bring 2-3 years of related experience to a challenging new role.

● Knowledgeable CRC adapt recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.

● Validated warehouse data structure and accuracy.

● Ability in screening processes. Source documentation. eCRF data entry ability.

● Organized and dependable candidate successful at managing multiple priorities with a

positive attitude. Willingness to take on added responsibilities to meet team goals.

● Familiarity with GCP, ICH and FDA requirements as they apply to clinical data.

● Extensive understanding of CDISC, CDASH and SDTM Standards. Ability and knowledge using EMR systems.

● Strong knowledge of the Drug Discovery or Drug Surveillance Processes.

● To seek and maintain full-time position that offers professional challenges utilizing

interpersonal skills, excellent time management and problem-solving skills.

● Dedicated to using excellent clinical research, investigation, and project management

abilities to optimize management, organization, and reporting of clinical data.

● Results-driven, precise and systematic with quick learning and collaborative nature. Strong

history with data management companies.

● Self-motivated professional accustomed to handling sensitive and confidential records while

thriving in deadline-driven environments.

● Polished in developing information systems for medical establishments to provide

top-quality care. Valued contributor focused on accurately capturing, storing, securing and

wielding healthcare data.

● Reliable employee seeking clinical research coordinator position. Offering excellent

communication and good judgment.

SKILLS

● SKILLS TECHINICAL SKILLS ● MS-OFFICE:

● Word, PowerPoint and

Excel, IOS

● Proficient in English

● Informed consent

● Site management

● Good Clinical Practices ● Medication dispensing ● Trial Management

● Patient Care

● Data Collection

● Clinical Research

● Active Listening

● Planning and Coordination

● Multitasking Abilities

● Analytical and Critical Thinking

● Organization and Time

● Research Sops Understanding

● Documentation Requirements Management

● Interpersonal Communication

WORK HISTORY

CLINICAL RESEARCH COORDINATOR- ( Onsite clinical solutions, NC)– (05/2022 to 06/2023)

● Coordinated and scheduled protocol-related in-patient visits that required testing of the IP to demonstrate vigilance in patient safety, protocol compliance and data quality.

● Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.

● Gathered and organized clinical trial documentation to meet rigorous standards for site approval.

● Created and maintained database and records filing system to document data on specimen collection, processing, and storage.

● Organized and maintained research study regulatory documents in site binder to maintain accuracy and integrity.

● Liaised with clinical investigator to identify, assess, and resolve site performance, quality, and compliance issues.

● Implemented electronic data capturing systems to adhere with clinical research guidelines.

● Processed sample storage and assay to provide registry of samples for test

development, validation, and analysis.

CLINICAL RESEARCH COORDINATOR (10/2020 to 11/2021) EHEALTHCONNECT PRIVATE LIMITED, Hyderabad, India

● Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.

● Collected data and followed research protocols, operations manuals, and case report form requirements.

● Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.

● Collected, evaluated, and modeled collected data.

● Followed informed consent processes and maintained records.

● Maintainedcompliancewithprotocolscoveringpatientcareandclinicaltrialoperations.

● Completed paperwork, recognizing discrepancies, and promptly addressing for resolution.

● Drove operational improvements which resulted in savings and improved profit margins.

● Worked to maintain outstanding attendance record, consistently arriving to work ready to start immediately.

● Actively listened to customers, handled concerns quickly and escalated major issues to

supervisor.

● Maintained excellent attendance record, consistently arriving to work on time.

● Led projects and analyzed data to identify opportunities for improvement.

Worked as a CRC for Gastrointestinal studies like Inflammatory bowel disease, Crohn’s disease randomized, double-blind, placebo- controlled clinical trials from 2020-2021 at Ehealth connect India.

CLINICAL PHARMACIST INTERN (07/2019 to 07/2021) ASTER PRIME HOSPITALS, Hyderabad, India

● Compared prescription details against safety standards and insurance requirements to support patients.

● Educated patients on possible drug interactions, potential side effects and optimal methods of administration.

● Used pharmacy software to enter prescription and insurance information.

● Counseled patients on new medications and OTC products.

● Communicated closely with patients, ensuring medical information was kept private.

● Helped patients overcome vaccine hesitancy by providing facts about efficacy and safety data.

● Recommended OTC devices or medication options to help mitigate individual symptoms.

● Followed department policies, procedures, and best practices for pharmacy operations.

● Assisted pharmacist in final review of filled prescriptions.

● Updated patient profiles and prescriptions in CLINEREX with strong focus on accuracy.

● Performed blood pressure and blood glucose tests on patients.

● Monitored inventory levels and notified pharmacist of items requiring reorder.

● Communicated with patients to collect information about prescriptions and medical

conditions or arrange consultations with pharmacists.

● Discussed medical histories with patients to provide most effective medical advice.

EDUCATION:

JNTU, HYDERABAD Doctor of Pharmacy, PHARMACY, 11/2021

D PROGRAME GRADUATE with extensive experience in Hospital pharmacy, Infusions and Hospital and Clinical pharmacy related practices. Completed INTERNSHIP in ASTER PRIME hospital for 1 year. Strong knowledge in Pharmacology, Therapeutics, Patient Medication Therapy Management and Prescription Drug Interaction Assessment. Proficient in hospital infusions. Responsible for patients care documenting and evaluating patients' medical history Provided specialized services to help patients manage co- morbidities and conditions such as diabetes, hypertension, asthma etc. Gained knowledge in areas of drug interactions, AFFILIATIONS medication adherence and patient counseling of prescribed medications Volunteered in conducting health care medical camps, patient counseling, adverse drug interactions monitoring and bedside patient monitoring and interaction.

● Research Project: STUDY TO COMBAT RESISTANCE TO ANTIBIOTIC WITH STEWARDSHIP

PROGRAM.

● 3.88-GPA.

ACCOMPLISHMENTS

● Participated in quiz competition in school, 2010, in many inter-school competitions -2017

● Race to optimize Antibiotic usage for better therapeutic outcomes, SYNCHROPHARMA-,

● INTERNATIONAL HACKATHON for Smart India Hackathon

● Certified Life Saver for Indian Red cross- 2015

● BloodBank-Certifiedlifesaver-2012

● Participated in National Pharmacy week

ADDITIONAL INFORMATION

● I am an organized and driven individual, with a clear desire to obtain professional development. Respected professional with experience in coding, maintaining medical charts and improving patient documentation. Offering decision- making, leadership and communication talents. Well-qualified CLINICAL RESEARCH COORDINATOR successful at building and maintaining secure, accurate and efficient data collection systems. Hardworking and pragmatic with strong attention to detail and methodical approach. Prepared to offer 2-3 years of experience to fast-paced position with room for advancement. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Dedicated to using excellent research, investigation, and project management abilities to optimize management, organization, and reporting of clinical data. Results-driven, precise, and systematic with quick learning and collaborative nature. Strong history with data management companies. Self-motivated professional accustomed to handling sensitive and confidential records while thriving in deadline-driven environments. Polished in developing information systems for medical establishments to provide top-quality care. Valued contributor focused on accurately capturing, storing, securing, and wielding healthcare data.

● First Aid /CPR Certified.

● BLS Certified.

Contact this candidate