As a healthcare professional with a qualification in M. Pharm / B. Pharm / BAMS / BHMS / BDS, you are invited to join our team in Mumbai. With 2 to 3 years of experience in drafting and reviewing PADER, PSUR, PBRER, and RMP, you will play a crucial role in our organization. Your responsibilities will include preparing and quality reviewing various types of Aggregate Reports (AR) such as PSUR, PBRER, Annual Safety Report, PADER, RMP, etc. You will also be involved in strategizing for the submission of ARs, arranging kick-off meetings with clients and relevant stakeholders, generating line listings and summary tabulations, and identifying and resolving issues. Additionally, you will provide support in other departmental activities. If you are a detail-oriented professional with a passion for healthcare and a strong background in aggregate reporting, we encourage you to share your CV with us at hr@fidelityhs.com. Join us in making a difference in the healthcare industry.,
Job Description: You will be responsible for checking the arrival of source documents and final signed off copies of aggregate reports. Additionally, you will need to keep a check on the online aggregate report tracker and assist with the analysis of action items populated in nonconformance. Qualification Required: - B Pharm, M Pharm, BHMS, BAMS Location: - Navi Mumbai Experience: - 2 to 4 years in safety writing & aggregate reports Please share your CV on hr@fidelityhs.com.,
As a Safety Data Exchange Associate at Fidelity Health Services, your role involves working on case processing and safety writing, with a focus on SDEA management. Your key responsibilities include: - Initiating communications with internal stakeholders such as business teams and subsidiaries to understand the requirements of SDEAs. - Following up with third parties/business partners to ensure SDEAs are in place. - Ensuring timely exchange of safety data with partners and conducting adverse event reconciliations. Qualifications required for this role include: - B. Pharm / M. Pharm/ BAMS/ BHMS degree. - Minimum 3-4 years of experience in case processing/ safety writing with knowledge of SDEA management. - Experience in exchanging safety data and conducting reconciliations with business partners. - Strong written and verbal communication / presentation skills. - Being up-to-date with the latest technical / scientific developments related to Pharmacovigilance. If you meet these qualifications and are looking to join a dynamic team, please share your CV on hr@fidelityhs.com.,
As a Health care professional (M. Pharm / B. Pharm / BAMS / BHMS / BDS), you should have 2 to 3 years of experience in drafting and reviewing PADER, PSUR, PBRER, and RMP. Your responsibilities will include: - Preparation and quality review of various types of Aggregate Reports (AR) such as PSUR, PBRER, Annual Safety Report, PADER, RMP, etc. - Strategizing for submission of ARs. - Arranging kick-off meetings with clients and relevant stakeholders like the ICSR team. - Generating line listings and summary tabulations by referring to processed ICSR for ARs and XML from a global safety database. - Identifying and resolving issues. - Providing support in other departmental activities. If you are interested in this position, please share your CV on hr@fidelityhs.com.,