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Clinical Research Coordinator Internship

Clinical Research Coordinator Internship

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Clinical Research Coordinator Certification – CRC Training & Placement Program

A (CRC), sometimes called a clinical trial manager, plays an integral role in medical studies of all kinds. They typically work under the direction of the principal investigator (PI), who is in charge of designing, conducting, and managing the clinical trial from a high level. It is the CRC’s job to support, facilitate, and organize daily clinical trial activities.

Clinical research coordinators also work in conjunction with the department, sponsor, and institution to guide them through compliance, finances, and personnel issues. In short, the CRC manages the day-to-day clinical operations activities, overseeing and executing delegated tasks to appropriate parties.

What is Clinical Trial Management System – CTMS

  • CTMS helps to maintain and manage the planning, performing, and reporting functions, along with participant contact information, tracking deadlines, and milestones.
  • This system maintains and manages the planning, performing, and reporting functions, along with participant contact information, tracking deadlines, and milestones.

    • Software’s In the Clinical Trial Management System:

    • Clinical Conductor CTMS
    • BioClinica CTMS
    • BSI CTMS
    • RealTime-CTMS
    • Ennov CTMS
    • DatStat CTMS
    • CoreValue CTMS
    • Intrinsic CTMS
    • MasterControl CTMS
    • LifeSphere CTMS
    • Clinical Studio

Roles And Responsibilities of Clinical Research Coordinator:

    Key responsibilities of the CRC include the planning and management of the study, enrollment, and maintenance, training initiatives, and maintaining compliance with federal, state, and institutional regulations. In addition, they carry out experiments, clinical research, and medical studies. They also engage directly with the trial participants as they screen them for eligibility, develop and implement recruitment strategies, and liaise with all teams throughout the trial. From evaluating research protocols to seeking approval from regulatory committees, CRCs have a broad reach within laboratories, medical centers, and research hospitals.

    Our  Interactive-CRC training program for Clinical Research Professional are designed for persons with or without prior on-site clinical trials experience, seeking qualifications and/or current practical knowledge to effectively work as a Principal Investigator (PI), Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Coordinator or Clinical Data Manager (CDM) in the monitoring of clinical trials globally in all countries that follow the ICH-GCP guidelines for conducting clinical trials. All courses include ICH-GCP certification.

    Prior to the start of the course, participants will receive comprehensive course material. Come to class prepared to interact – you will be able to ask questions, provide feedback and participate in discussions and group work. Upon course completion, participants will be provided training certificates.

Program Objective:

  • Describe the drug development process, the importance of Good Clinical Practice, and the roles and responsibilities of the research team
  • Define the regulatory requirements, explain the differences between ICH and FDA guidelines, and describe the elements of a protocol
  • Outline required elements of the informed consent
  • Identify the investigational product accountability requirements and impact of the reconciliation process on the study
  • Define the safety definitions and comprehend the safety reporting requirements
  • Prepare for and complete source document verification
  • Perform the steps involved in monitoring the study pre-visit, during the visit, and post-visit
  • Create cohesive, well-written protocol deviations and action items, and accurately complete the monitor visit report and site follow-up letter
  • Define the impact of quality assurance and audits in clinical research

CRC Course syllabus

Module 1: Drug Development Process, Good Clinical Practice (GCP), and Clinical Research Team Roles and Responsibilities

Module 2: IRB, Clinical Study Protocol Elements and Amendments

Module 3: Informed Consent

Module 4: Investigational Product Accountability

Module 5: Safety Definitions and Reporting Requirements

Module 6: Source Document Verification

Module 7: Monitoring the Study

Module 8 and Module 9: Monitoring Visit Reports and Contact Reports

Module 10: Regulatory Compliance and Quality Assurance: Audits and Inspections

Eligibility for CRC Certification Program:

  • Any Graduate/ B.tech/ B.Sc. in Microbiology/ Life Sciences/ Botany/ Zoology/ Food Science/ Food Technology/ BE/ B.Pharma/ MBBS/ BDS/ BHS/ BUMS/ BAMS or any other discipline. Diploma holders are eligible for our Executive Diploma, Industry Certificate, and Certificate Programmes.
  • To secure a job as a CRC, professionals must have at least a four-year bachelor’s degree in a field such as medical technology, microbiology, or public health administration. However, some employers require an additional two-year master’s degree, particularly for management positions.

Clinical Research Associate VS Clinical Research Coordinator:

A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a research professional with a minimum of a bachelor’s degree (usually nurses!) who works under contracts or is hired by sponsors, CROs, or freelancing (by biopharma and research institutes) to perform roles listed in ICH GCP guidelines for monitoring clinical trials.
When a PI (principal investigator, i.e. often a busy, working physician running a trial on the side) is chosen to conduct a trial at their site, clinical research coordinators often take over part of the essential responsibilities of PI. This includes making sure the trial is:
  1. Conducted
  2. In compliance with the protocol and federal or international regulations

Programme Deliverables

  • A comprehensive study material for all the modules in hard copies ensuring the needs of the audience. The accompanying CRC online training material is appropriately aligned with the current Industry’s expectations.
  • Assignments for all the programme modules for continuous evaluation and guidance.
  • Interactive or online live sessions on all key areas of the programme giving all flexibility to the participants.
  • CRC Online classes for all the modules will be conducted on the weekends. Moreover, a doubt clearing session will also be scheduled before the examination.
  • All the efforts are made by IGMPI faculty members to make the entire programme modules easily understandable.
  • Clinical trail program Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job.
  • At the end of each programme modules, the trainers shall obtain feedback from the participants using specially designed questionnaires.

Interview Preparation Sessions

  • Participants who have completed the Clinical Research Coordinator course training will be put under our Placement Incubation Program. As part of this program, participants will undergo a thorough CRC interview preparation process. A huge repository of Clinical Research Coordinator Interview questions with answers will be provided for the participants to prepare after CRC online Certification. A dedicated Clinical Research Coordinator Expert Trainers (SME) will help in resume building, conduct mock interviews and evaluate each participant’s knowledge, expertise and provide feedback. Clinical Research coordinator Resume Samples will be given and the participant should Update With Clinical Research coordinator Skills. Our SMEs will do the necessary handholding on Clinical Research coordinator interview preparation process till the time the participant is placed in Clinical Research Companies in Hyderabad,Pune Mumbai and Bangalore etc. Guidance is also provided on Linkedin profile building and tricks of the trade to improve the marketability of the resume. – Clin Infotech Management.

Assessment & Certification

    All the participants are expected to appear online assessment . After successful completion the participants will be certified as professional in Clinical Research Coordinator (CRC) by Clin Infotech. For all the above mentioned elaborate study resources, Assessment test papers and case studies would be provided by the Institute from time to time. Details get updated on the webpage as well. The CRC certification will be awarded after the required levels of knowledge, skills, professionalism and attitude are assessed through the Clin Infotech assessment process.

Placement Assistance & Corporate Relations

    In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc. The IGMPI’s Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare and Food industries on regular basis.

Clinical Research coordinator Companies

    IQVIA, Covance, Parexel, Asiatic clinical Research, Astron research, BioAxis, Bioclinica, Axis Clinical, Croissance, Dubar Research foundation, Eresearch technologies, Global clinical Trials, GVK Biosciences, Kemwell Biopharma, Labcorp, Lambda Therapeutics, Makro care, Navitas Life Sciences, Novotech, PPD, Sai Life Sciences, Spectrum Clinical Research, Strides Pharma Research symphony, syneos Health Care, Syngene, Techobserver, Vedic  Life sciences Etc.

    Why CLIN INFOTECH?

    1. Clin Infotech is a leading training institute in the field of Advance Clinical Research Training Program. Here's why you should choose us:
    2. Industry-Experienced Faculty: Our instructors are seasoned professionals with extensive industry experience, ensuring that you receive practical insights and real-world perspectives.
    3. Hands-on Approach: We emphasize a hands-on learning approach, enabling you to apply theoretical concepts to practical scenarios.
    4. Customized Learning Paths: Our programs are designed to cater to learners of various backgrounds and skill levels, allowing you to learn at your own space.
    5. Job Placement Assistance: We provide comprehensive job placement assistance to help you secure lucrative career opportunities in the IT industry.

    Our Alumni Work At:

    Our alumni have successfully secured positions in leading organizations. Their achievements reflect the quality of our training programs and the practical skills they gained during their time with us.

    Eligibility:

    Minimum Eligibility Criteria For Application To The Course Would Be Either Of The Following:

    Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) and all professionals working with Pharmaceutical companies, CROs and Hospital.

    Admission Process:

    The admission process for the Medical Writing Course with 100% placement assistance is very simple. Candidates can apply online through our website. After examining your application our executives contact you to complete the further procedure.

    At Clin Infotech Systems, we are committed to assisting you every step of the way with our user-friendly online application process and committed admission officers. Prepare yourself to begin a fulfilling career in Medical Writing with our thorough admissions procedure.

    Step 1: Apply Online at https://www.clininfotech.com

    Step 2: Review the Application

    Step 3: Contact and Further Process

    Step 4: Enrolment and Confirmation

    Step 5: Course Completion

    Step 6: Assessments and Assignments

    Step 7: Mock Test and Mock Interview

    Step 8: Resume Preparation

    Step 9: Skill Development

    Step 10: Placement Assistance

    Trainers and Training Process

    At Clin Infotech, we have the best faculties with 15+ years of real-time experience in the clinical research industry. The course curriculum is specially developed with respect to the current industry trends and standards. Students will have the access to our online sessions. Additionally, the students will get a chance to clear their doubts on alternate weekends. Also, the practice interview sessions are also conducted by our trainers followed by timely assessments.

    The trainers will help our students to pass their interviews smoothly and get placed in a good company.

    Clin Infotech Advantage:

    1. Complete Course Material will be provided including detailed information about the entire workflow of a Clinical Research Associate.
    2. 2 months internship available after rigorous training in Medical Writing.
    3. Own CRO live projects.
    4. Highest placement record across all training institutes.
    5. Industry-based SOPs training.
    6. Trainers with a minimum of 7+ years of experience.
    7. Comprehensive teaching by medical doctors.
    8. Hands-on training will be provided on clinical research sites.

    Our team of experienced drug safety specialists also provides the following services upon successful completion of the training:

    1. Resume Preparation
    2. Interview Preparation with real-time questions and answers
    3. Mock Interview Sessions
    4. Communication Skills and Personality Development Sessions
    5. Placement Assistance
    6. Placement Assurance

    It's time to comprehend and put standard trail management ideas into practice in order to build a solid methodology for the evaluation and boost the timely completion of crucial trials for the benefit of patients. To plan, produce, monitor, and complete all project duties, you must acquire specific skills and knowledge.

    Through its comprehensive certification program, Clin Infotech offers thorough instruction in clinical research throughout the whole clinical trial process. With the help of this clinical trial management course, instructors will make sure that students have a procedural and administrative understanding of the clinical trial process as well as the capacity to advance their knowledge and abilities.

    This curriculum will teach you the whole Regulatory responsibilities involved in Document Creation; Planning, Organizing, Monitoring, Recording, Analysis, and Reporting of Human Clinical Trials, as well as the most recent discoveries and specialties in e-Clinical Technology.

    Enroll Now!!

    Take advantage of this opportunity to engage with cutting-edge industry technologies and learn how to apply them in the domain of Clinical Trial Management.

      Certification:

    • Certificate will be provided for this Course on successful completion of Assignments & Projects.
    • Certificate would be awarded at the end of the program by Gratisol Labs. A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry.

    For more information, please contact Clin Infotech at careers@clininfotech.com or 8374457387

      Ready to Apply For a Job Immediately After Your Internship