Job Description
Read and understand Curation Protocol requirements.
Perform literature search - develop comprehensive search strings and screen abstracts for inclusion.
Develop source dataset Tabulate all search results, review and select references, track inclusions and exclusions.
Conduct a sample extraction that cover maximum scope in order to review and finalize the specifications of outcomes dataset
Extract data from full text articles:
Trial design, treatments, demographics and outcomes data (biomarker, efficacy, safety and quality of life outcomes) from clinical literature. Extract data from graphs for outcomes reported on linear or logarithmic scales with precision. Develop outcomes dataset Curate data, standardize curated data as per the requirements and specifications, perform QC checks and finalize for meta-analysis. Present and communicate data to stakeholders Identify any advance process improvement opportunities Conceptualize and contribute towards automation initiatives Maintain and enhance therapeutic area knowledge including, disease state and compound for assigned project. Maintain comprehensive knowledge of Clinical trials. Stay current with external environment and emerging technologies Proactively share knowledge and promote a culture of excellence Be a team player Minimum Qualification Requirements:
Masters Degree with:
At least 2-3 years of experience in systematic literature review and scientific research. Hands-on experience in data curation and exposure to quality check (QC) is an advantage. Familiarity with the use of controlled vocabularies and ontologies in clinical research and experience with reading and comprehension of scientific journal literature. Knowledge of drug development process, clinical study designs and basic statistical concepts used in clinical trials. Development of summary level Clinical Trial Outcomes Datasets for meta-analysis. Cognitive abilities including; verbal reasoning, attention to detail, critical thinking, and analytical ability. Excellent verbal and written communication skills are essential along with the ability to express thoughts logically and succinctly. Demonstrated project management and time management skills. Strong interpersonal skills and the ability to be flexible in varying environments and with multiple customer groups. Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates) particularly Excel. Contribute to process improvements, suggesting opportunities where appropriate Other Information/Additional Preferences:
Other Information:
Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience (e.g., neuroscience, immunology, oncology, or endocrine expertise) Statistical analysis and ability to learn analytics tools. Ability to work well independently and as part of a team. Limited travel, up to approximately 10%. Additional Preferences:
Ability to work well across cultures and time zones. Masters degree in a research focused discipline
Please sharee your updated CV to bh*******y@re**********a.com Job Classification
Industry: Pharma, Biotech, Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology,
Role Category: Drug Regulatory Affairs/Documentation
Role: Drug Regulatory Affairs/Documentation
Employement Type: Full time
Education
Under Graduation: BVSC in Veterinary Science, B.Sc in Any Specialization, B.Pharma in Pharmacy, MBBS in Medicine, BDS in Dentistry
Post Graduation: Any Postgraduate in Any Specialization, Post Graduation Not Required
Doctorate: Any Doctorate in Any Specialization, Doctorate Not Required
Contact Details:
Company: Recruise India
Location(s): Bengaluru
Keyskills:
Communication Skills
outcome data set
Clinical Research
Project Management
Clinical Pharmacology
Data Curation
Systematic Literature Review
Medical
Drug Development
Clinical Trials
Data extraction