Responsibilities Qualifications Bachelor’s Degree in scientific discipline or Business Informatics or similar area with 1-2 years of directly related experience; Preferred Qualifications: Apply : https://international-medpace.icims.com/jobs/8292/safety-database-specialist/job?hub=6
Discy Latest Articles
Study Start up Submissions CoordinatorClinicalresearchinfo
Responsibilities Qualifications Apply : https://international-medpace.icims.com/jobs/8533/study-start-up-submissions-coordinator/job?hub=6
IRT programmer -Entry levelClinicalresearchinfo
Responsibilities Qualifications Apply : https://international-medpace.icims.com/jobs/8560/irt-programmer–entry-level/job?hub=6
Core Lab Clinical Database ProgrammerClinicalresearchinfo
Responsibilities Qualifications Apply : https://international-medpace.icims.com/jobs/8702/core-lab-clinical-database-programmer/job?hub=6
Clinical Specialist – MSD (Chennai)Clinicalresearchinfo
Job Description: Summary: Function as “Professional Services Manager” in the critical and chronic care solutions division of the Health Care group. The position is based out of Chennai and will be responsible for the southern region of India. Work week ...
Project Coordinator 1Clinicalresearchinfo
Responsibilities as Project coordinator: Educational Qualification: BPharma, MSc Technical/functional Skills: Experience: 0-3 years Behavioral Skills: Apply : https://career10.successfactors.com/career?career%5fns=job%5flisting&company=syngeneP1&navBarLevel=JOB%5fSEARCH&rcm%5fsite%5flocale=en%5fUS&career_job_req_id=54173&selected_lang=en_GB&jobAlertController_jobAlertId=&jobAlertController_jobAlertName=&browserTimeZone=Asia/Calcutta&_s.crb=0JnT5KucdlPJBVbb8iYZJM9IZStQKl0XXbglIHn9VXo%3d
Mandatory expectation for all roles as per Syngene safety guidelines Key Responsibilities: Educational Qualification & Experience MSc (Polymer Chemistry) with 0 -3 years Technical/functional Skills: Apply : https://career10.successfactors.com/career?career%5fns=job%5flisting&company=syngeneP1&navBarLevel=JOB%5fSEARCH&rcm%5fsite%5flocale=en%5fUS&career_job_req_id=54239&selected_lang=en_GB&jobAlertController_jobAlertId=&jobAlertController_jobAlertName=&browserTimeZone=Asia/Calcutta&_s.crb=0JnT5KucdlPJBVbb8iYZJM9IZStQKl0XXbglIHn9VXo%3d
Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments ...
Project Support CoordClinicalresearchinfo
Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. – Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. – Ensures allocated tasks are performed on time, within ...
Feasibility Data ScientistClinicalresearchinfo
Roles and Responsibilities: • Recognize, exemplify and adhere to ICON’s values which center around our commitment to People, Clients and Performance.• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement ...
JOB-DESCRIOTION Essential Duties and Responsibilities include the following. Other duties may be assigned. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ...
Responsibilities Education/Qualifications Experience/Skills Preferred Apply : https://careers.labcorp.com/global/en/job/2329925/Data-Analyst
Centralised Study Associate IClinicalresearchinfo
Experience Minimum Required: Education: University/College degree (Business or Accounting preferred) AND three 0-1 years work experience in a financial, clinical trial, or grant payment position. Apply : https://careers.labcorp.com/global/en/job/235482/Centralised-Study-Associate-I
Clinical Research Assoc IClinicalresearchinfo
Job Description Qualifications • M.Pharm pharmacology / B.Pharm+M.Sc. in Clinical Research • Should have 2-3 Years’ experience of monitoring clinical trials. • Experience in monitoring the clinical trials which includes SIV, SMV, SCV & Site selection visit • Travelling included ...
Feasibility Site SpecialistClinicalresearchinfo
A day in the Life: Education Experience Apply : https://jobs.thermofisher.com/global/en/job/226490/Feasibility-Site-Specialist