RAY is an outsourcing service provider dedicated to the Drug Development Process from phase II trials through phase IV in addition to post-marketing surveillance studies. Our Clinical Research Professionals RAY has access to a large clinical research resource pool spanning the Middle East region. Our range of clinical professionals includes, Project Management , Project Management Assistants, CRAs, CTAs, Medical Advisors, Medical Writers, Quality Assurance Professionals, Biostatistics and Data Management staff - a combination of experienced people, scientific excellence and state-of-the-art facilities.Responsibilities -Responsible for managing clinical trial databases including database design and maintenance, managing electronic data transfers, study randomization coordination, and programming of data rules, checks, listings, and reports.-Train team members on selected tasks-Lead database audit team.-Develop and test databases and edit specifications-Track and integrate queries-Develop and maintain good communications and interpersonal relationships with the team.-Prepare Data Validation Specification -Support Clinical Data Management activities (e.g., review of CRF design and data queries, CRF-tracking, coding, and locking).-Utilize current study documentation including protocol, Case Report Forms (CRFs) etc.-Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action-Track and integrate queries-Assist in early and final database QC activities-Ensur successful delivery of his/her direct report's project deliverables, on time with high quality. -Manage and develop the team to ensure their performance meets and /or exceeds both the business and their own personal goals/objectives-Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practice, Regulatory Agency requirements and Ray SOPs.-Perform other duties as assigned.

RAY is an outsourcing service provider dedicated to the Drug Development Process from phase II trials through phase IV in addition to post-marketing surveillance studies. Our Clinical Research Professionals Responsibilities:-Responsible for managing clinical trial databases including database design and maintenance, managing electronic data transfers, study randomization coordination, and programming of data rules, checks, listings, and reports.-Take responsibility for specific tasks on projects, or acts as the main CDM contact on individual projects-Train team members on selected tasks-Write and resolve data clarifications.-Lead database audit team.-Develop and test databases and edit specifications-Track and integrate queries-Prepare Data Validation Specification -Support Clinical Data Management activities (e.g., review of CRF design and data queries, CRF-tracking, coding, and locking).-Utilize current study documentation including protocol, Case Report Forms (CRFs) etc.-Generate and close queries or apply self-evident corrections to the data according to the relevant guidelines-Identify and report protocol violations-Review Manual and Patient Profile, issue queries-Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action-Track and integrate queries-Assist in early and final database QC activities-Ensure successful delivery of his/her direct report's project deliverables, on time with high quality. -Provide technical support to team members to ensure that they have the required knowledge to fulfill their duties.-Manage and develop the team to ensure their performance meets and /or exceeds both the business and their own personal goals/objectives-Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practice, Regulatory Agency requirements and Ray SOPs.-Perform other duties as assigned.

DataClin is a contract research organization with extensive experience that captures the full workflow of Clinical Data Management, Biostatistics and Medical Writing processes on both clinical trial and post marketing observational studies; the diversity of projects includes world’s leading pharmaceuticals organizations.DataClin offers experienced solutions and services across a broad spectrum of therapeutic areas, including:•Protocol design & review•Randomization schedules•Edit check specifications•Database design, build and test•Data management plan•CRF designing, annotation, completion guidelines•Data validation /verification guidelines•Data entry guidelines (Single and double data entry)•Query management•Coding services•SAEs reconciliation•Medication and laboratory•Quality analysis•Database lock / freeze and transfer•Generation of data listings•Migration of databases•Quality management procedures•Analysis and reporting of pre-clinical and Phase I-IV•Publications: Manuscripts, review articlesDataClin services are given end to end or in part as required by the client.DataClin services and systems are governed by well defined quality assurance structure where regulatory requirements such as ICH/GCP, FDA 21 CFR Part 11 and EMA- EudraLEX and other customer specific standards are respected.We at DataClin strive to provide effective solutions to our partners’ R&D investments in a true sense of ownership, accuracy and affordability.Our team comprises of outstanding talent medical personnel with broad experience in International Clinical Trials and Data Management guidelines. Our team members have experience in working across multiple therapeutic areas and all of them are extensively trained in ICH-GCP.DataClin has the ability and resources to work around the clock, allowing reduction in cycle times and achievement of rapid database locks, allowing our clients to meet and exceed timelines.

• Dispensing prescription medicine to public.• Ensuring that different treatments are compatible.• Checking dosage and ensuring that medicines are correctly and safety supplied and labeled• Arrange the delivery of prescribed medicine to patients.• Budgeting and financial management.• Keeping up to date with current pharmacy practice, new drugs and their uses.