Job Summary: We are seeking an entry-level Sales Associate to join their team. The primary function of this position is to support the sales team with marketing campaigns. This position researches contact information for physicians and clients who are potential clients to join the health insurance network. The ideal candidate will be self-driven, detail oriented, and experienced with multi-tasking.Day-to-day RolePlace follow-up calls to clinical and fitness practitioners after recruiter s initial outreach.Cal to coordinate field appointments.Handle inbound calls as needed during high call volume times.Handle typical objections and present information utilizing campaign scriptsInteract in a positive, respectful mannerEstablish and maintain cooperative working relationships.Quickly navigate internal databases, as well as search internet sites for informationDemonstrates accuracy and focus in a fast-paced environment.

Process medical dataEnsure the patient demographic details are updated appropriatelyVerification of the patient data mentioned in the medical claimsEnter charges and post payments in the softwareEnsure Report submission and verifications

CMC Regulatory Affairs AssociateOur client, a global pharmaceutical organisation based in Cork are currently recruiting for a CMC Regulatory Affairs Associate to join their global regulatory affairs group on a permanent basis. As CMC Regulatory Affairs Associate you will partner help build and manage submission content, provide guidance on structure and content placement within Common Technical Document (CTD) registration submissions.Responsibilities- Lead CMC submission management process by providing knowledge of CMC regulatory requirements- Comprehensive knowledge of ICH CTD and evolving global agency standards, of CMC RA submission processes, electronic submission regulations and guidance regarding structure requirements to CMC development teams regarding global CTAs and registration dossiers- Responsible for preparing CMC CTD content consistent with approved manufacturing changes, technical reports and procedural requirements- Partner with the CMC RA Scientist to plan and prepare submission content to support clinical studies and manufacturing process changes for development and marketed products- Partner with the CMC RA Scientist to drive the execution of submission planning for global registration and maintenance submissions- Implement and in some cases interpret global regulations and guidance’s and look to regulatory precedence into submission processes and publishing standards to ensure final document content and structure are aligned with local regulatory requirements.- Partner with other regulatory staff, as necessary, to gain alignment on establishing new submission standards to meet local agency requirements- Leverage internal forums to continue to develop and share regulatory and drug development expertise to meet critical product registration timelines and electronic submission structure and content requirements.