Clinical Research Executive Jobs

We are seeking a highly motivated Clinical Research Executive to assist in the planning, execution, and management of clinical trials. The role involves coordinating research activities, ensuring regulatory compliance, and collaborating with cross-functional teams to ensure the smooth execution of clinicalstudies.

Lenskart Optical is the premier destination for optical services at various Kerala locations. With the best optician in the area, we deliver top-notch eye care services to our customers.The Optometrist will be responsible for conducting eye exams, diagnosing and treating vision problems, prescribing corrective lenses, and providing personalized eye care services to patients.QualificationsStrong clinical skills in conducting eye exams and diagnosing vision problemsProficiency in prescribing and fitting corrective lensesExcellent interpersonal and communication skillsDetail-oriented and able to work in a fast-paced environmentBachelor's degree in Optometry or related fieldValid license to practice optometryContact HR: 7034659150

Dear CandidateWe are looking for Trainer for our academy in Deepam Hospitals.Please contact 9361069144 for more details.RegardsHR

Dear Everyone,Today's Greetings!!We are now looking for a Senior Clinical Research Associate. The specifics are provided below.Clinical operation departmentSenior Clinical Research Associate is a job title.Experience: 27 yearsBachelor of Pharmacy/Master of PharmacySalary: According to corporate policy.Immediate joining/one month's noticeWork mode: work from officeHyderabad is the location.Local candidates are preferred.

Position: Clinical Research CoordinatorQualification Bio Science (B.Pharm/Bio Tech etc.)Experience Above 1 Year (Clinical Research Experience must) Timing General ShiftSalary 2L 2.5L (Per annum)Location Visakhapatnam/Chennai/BangaloreLanguage Know English/Kannada/TeluguJOB Description Clinical Research Coordinator To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Coordinate between the local/Central laboratory and courier for the shipment. Assist the pharmacist in drug accountability and temperature maintaining logs. Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report Sr.DGM daily and take advice for further action.

1) Identify new sites. PIs and conduct the detailed protocol specific feasibility.2) Preparation for site selection visit3) IRB submission & approval4) Regulatory document collection5) Set-up. maintain & timely update or Trial Master File(TMF) & relevant site binders Files6) Prepare site for Site Initiation Visit (SIV)7) Assisting Principal Investigator in administering the Informed Consent Form process8) Ensure protocol adherence and Compliance; t document protocol deviations as appropriate and communicate any impacting subject safety to !he Ethics Committee. 9) Pre-screening, screening, enrolling & recruiting subjects.10) Creating and Preparing Source Documents and their templates11) Coordinate and schedule subject's regular follow-up Visit and Procedures. preventing lost to follow-up & missed visits. Maintaining regular contact With Subject Telephonically12) Manage Clinical Trial Materials (CTM ). accountability, distribution & logistics at site13) Filling the case reports forms and Electronic case report forms and resolving all data queries within timelines.14) Reporting and coordinating all Adverse Events & Serious Adverse Events according to their timelines.15) Filling up and maintaining trial related logs like drug dispensing logs, subject logs. investigational Product t Logs, temperature logs. Etc. 16) Maintaining Calibration records of Instrument used for the trials.17) Preparing Site for monitoring & audit visits. Coordinate close out visit & archival at site.18) Communicating all protocol-related issues problems to the appropriate management staff including but not limited to questions regarding the conduct of clinical trials. Concerns regarding possible serious adverse events or subject compliance.19) Co ordinate central lab logistics & sample flow. Review lab data & communicate abnormal values to the primary care provider(if appropriate) & investigator.20) Co ordinate subject reimbursements.21) Performing all the above activities i

1.Prepare, conduct and report on activities related to the completion of site selection, initiation, routine monitoring and close-out visits2.Monitor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level3.Perform source data verification and follow up on data queries at the site level, on-going review of any 4.Risk Based Monitoring related information influencing data quality and frequency of site visits5.Ensure accurate and timely reporting and follow up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations6.Act as the main line of communication between the Sponsor and the site.7.Be a point of contact/liaison for in-house support services and vendors.8.Ensure proper handling, accountability and reconciliation of all Investigational Product(s) and clinical study supplies9.Review the status and contents of essential documents at the site level and reconcile study OSF/ TMF at site and/or country level.10.Experience in all types of monitoring visits.

Oversight of externally and internally sourced data management Development of clinical testing systems, include documentation, implementation and report Must be self-motivated, with the ability to follow through on assignments without direct supervision, very attentive to detail, capable at multitasking across projects and able to effectively contribute in a team environment Should have the ability to deal with electronic format of clinical data Strong Analytical skills to facilitate detecting and resolving data problem encountered in clinical research studies. On-site training will be provided.Candidates ProfileB.Pharm or a basic science degree. Should have good presentation and good communication skills , majorly in English Ready to work in rotational shiftsOffice Address:RDB Boulevard, 4th floor, Plot- K 1,Block- EP & GP,Salt Lake, Sector-V,Kolkata - 700091.

Need a Clinical assistant for Clinical trial research work