Landmark Research, a leading CRO, is dedicated to advancing clinical research through education and training. The organization offers a comprehensive range of certificate courses tailored to enhance professional skills and deepen knowledge in several specialized areas of clinical research. These courses are meticulously designed to meet the evolving needs of the industry and provide practical, hands-on experience alongside theoretical learning. Each program is led by experienced industry professionals who bring real-world insights into the classroom, ensuring that participants are well-equipped to excel in their respective fields.
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The clinical research course at Landmark Research offers a thorough grounding in the essentials of clinical research, covering study design, methodology, ethical considerations, and regulatory requirements
Participants will gain insights into the various phases of clinical trials, understand the critical aspects of data collection and analysis, and learn the roles and responsibilities of clinical research professionals
This course is designed to equip learners with the necessary skills to effectively manage and conduct clinical trials, adhering to good clinical practice (GCP) and other regulatory guidelines
The Pharmacovigilance course is designed to train participants in the monitoring and assessment of pharmaceutical product safety
The program covers adverse drug reactions, risk management, and the regulatory aspects of drug safety reporting
Students will acquire the skills needed for adverse event reporting, signal detection, and risk assessment, ensuring they can effectively contribute to the safety and efficacy of pharmaceutical products in compliance with regulatory standards
Landmark Research’s medical writing course trains the participants to produce precise, accurate, and compliant clinical documents
The curriculum covers scientific writing principles, the structure and content of clinical study reports, and the creation of regulatory documents
Participants will learn to write for regulatory submissions, conduct literature reviews, and synthesize information ethically and effectively, preparing them to meet the high standards required in clinical research documentation
The Biostatistics course comprehensively introduces the statistical methods used in clinical research
It encompasses basic and advanced statistical techniques, including hypothesis testing, regression, and survival analysis
This course is tailored to help participants analyze clinical trial data rigorously, providing them with the statistical tools necessary to interpret results and make informed decisions in the clinical research process
The regulatory writing course at Landmark Research provides specialized training in creating essential documents for regulatory submissions
This course covers the preparation of clinical evaluations, clinical investigations, and comprehensive regulatory documents in line with global standards
The training emphasizes the importance of adhering to regulatory requirements, ensuring document accuracy, and maintaining ethical standards in clinical regulatory writing
Landmark Research’s clinical data management course delves into the intricacies of managing clinical trial data
The curriculum includes database design, data entry, and data validation, emphasizing the use of software tools to ensure data integrity and regulatory compliance
Participants will learn to develop data management plans, design case report forms (CRFs), and implement electronic data capture (EDC) systems, preparing them to handle clinical data with accuracy and efficiency
Eligibility
The minimum eligibility criteria for enrolment in the online course would be either of the following:
MBBS | BAMS| BDS| BHMS| Physiotherapy and occupational therapy graduates
B.Pharm/M.Pharm graduates/ Post graduates in sciences/life sciences/ biosciences with any of the following subjects-chemistry, botany, zoology, biochemistry, microbiology, genetics, and biotech.
What are future career opportunities in CRO in India?
- Pharmacovigilance specialist
- Clinical research associate (CRA)
- Clinical trial associate
- Data analyst/scientist
- Pharmacovigilance consultant
- Medical writer
- Medical coder
- Regulatory affairs officer
Sectors where candidates can find opportunities
Candidates who have completed pharmacovigilance courses will be placed in the following sectors
- Biotechnology company
- Clinical data management companies
- Pharmacovigilance centres
- Pharmaceutical companies
- IT companies in healthcare
- Knowledge process outsurcing such as Accenture, Quintiles, etc.
- Clinical CRO (contract research organization)
- Data management CROs
- Packaging labeling and contract manufacturers
- Regulatory agencies such as DCG (I) & CDSCO