Assoc. dir., clinical data mgmt page is loaded assoc. dir., clinical data mgmt apply remote type hybrid locations col - cundinamarca - bogotá (colpatria) time type full time posted on posted 18 days ago time left to apply end date: august 22, 2025 (5 days left to apply) job requisition id r353934 job description under the direction of the global data operations (gdo) leadership, the gdo operations manager is responsible for leading senior clinical data managers (scdms) and clinical data managers (cdms) in operations tasks, both strategic and tactical in nature, within a data management center (dmc). they are responsible for ensuring the consistent execution of quality processes and deliverables and managing the workload and development of their direct staff. encourages effective interaction of dmc staff with business partners to achieve common objectives. primary activities include, but are not limited to: direct line management of scdm and cdms. talent management and performance management of teams with more than 10 members escalates to appropriate leadership/management as needed as risks and needs arise in the business increases functional effectiveness by supporting departmental efforts to simplify and standardize procedures to the greatest extent possible, sharing best practices and participating or leading in continuous improvement efforts. participates in or leads gdo business excellence networks (bens)gdo improvement efforts, gdo and/or gdms special initiatives as needed facilitates and/or participates in management and functional area meetings, contributing expertis...
Pharmacovigilance specialist page is loaded pharmacovigilance specialist apply remote type hybrid locations col - cundinamarca - bogotá (colpatria) time type full time posted on posted 3 days ago time left to apply end date: august 15, 2025 (5 days left to apply) job requisition id r360613 job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, p harmaceutical chemist * 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety repo...
Senior manager data integration page is loaded senior manager data integration apply remote type hybrid locations col - cundinamarca - bogotá (colpatria) time type full time posted on posted 12 days ago time left to apply end date: july 31, 2025 (2 days left to apply) job requisition id r352979 job description join our dynamic team as a senior manager data integration! in this role, you will play a vital part in leading and directing our functional area. you will be responsible for overseeing business deliverables, interpreting performance metrics, and ensuring the success of your team while aligning objectives with the broader goals of the organization. we are seeking a motivated individual who is passionate about fostering team development and driving performance. if you possess strong leadership capabilities and are ready to take the next step in your career, we encourage you to apply and join our innovative environment focused on excellence. key responsibilities: lead and manage direct reports, setting priorities and developing performance objectives that align with organizational goals. assign work and ensure team members receive necessary training for effective performance. motivate staff by managing workloads realistically, anticipating challenges, and elevating complex issues when needed. conduct regular performance assessments, provide constructive feedback, and facilitate annual appraisals for your team. support career development by collaborating with staff on development plans and growth opportunities. participate in recruiting efforts and may supervise continge...
Pharmacovigilance specialist page is loaded pharmacovigilance specialist apply remote type hybrid locations col - cundinamarca - bogotá (colpatria) time type full time posted on posted 3 days ago time left to apply end date: august 15, 2025 (5 days left to apply) job requisition id r360613 job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, p harmaceutical chemist * 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conduct...
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