Clinical Research Coordinator Fresher Jobs in Chennai

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Job descriptionPosition title: Manager- Sales And Marketing (Pre Engineered Buildings)DescriptionFunction : Sales and Business Sales / Business Development/Direct SalesResponsibilities Candidate will be responsible for sales of Pre Engineered Steel Buildings Pan India. Past Experience in the PEB industry. Should be technically sound to have meetings with Architects/Consultants and Clients. Should Belong to the industry having a strong network with various clients. Exploring new markets and business from existing customers all over india. Maintained, Developed and increased customer base and followed up with customers for their New upcoming projects. Handling sales of product & services to prospective customers, keeping the view of the defined targets. Tracking Market/ competitor trends to keep abreast of the changing clients requirement/expectations. A keen planner , strategist & implementer with demonstrated abilities in devising marketing activities and accelerating business growth Proven track record of success in the sales cycle from plan to close good communication, interpersonal, and organizational skills extensive travel, exposure to work sales and marketing with peb co.Immediate joiners will be preferred: Please mention PEB Site Engineer Profile in the subject line.Salary:The salary for this position will be commensurate with experience and qualifications.Application Process:To apply for this position, please submit your resume and cover letter to [Insert contact information]. We thank all applicantsContact:- Tejashwani V - Mobile no:- +91 89258 27724 - email:- tejashwanitrs@gmail.com

Position Clinical Research CoordinatorQualification B.PharmExperience - Above 1YearsTiming - General ShiftSalary Based upon PerformanceLocation ChennaiLicence: Pharmacy Lice(Only B. Pharm is eligible for this Job)Job 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 the Site Head in the managing the Site to ensure ethical conduct of research activities. Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. Provide guidance to 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. Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Assist the pharmacist in drug accountability and temperature maintaining logs. Monitoring Sr. CRC and 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 to the Site Head daily and take advice for further action. Delegate the work to Senior/Junior/Trainee CRCs as per the requirement.Job Types: Full-time, PermanentSalary: ?10,000.00 - ?15,000.00 per month