Clinical Operations Manager

1 semana atrás


Sao Paulo, Brasil MSD Tempo inteiro

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally.

Under the oversight of the Sr. COM, Head COMs or CRD, the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.

**Responsibilities include, but are not limited to**:

- Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA).
- Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Financial forecasting in conjunction with Sr.COM /other roles.
- Executes and oversees clinical trial country submissions and approvals for assigned protocols.
- Develops local language materials including local language Informed Consents and translations. Interacts with IRB/IEC and Regulatory Authority for assigned protocols.
- Manages country deliverables, timelines and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.
- Contributes to the development of local SOPs. Oversees CTCs as applicable.
- Coordinates and liaises with CRM, CTC, CRA, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
- Collaborates closely with Headquarter to align country timelines for assigned protocols.
- Provide support and oversight to local vendors as applicable.
- Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management. Enters and updates country information in clinical and finance systems.
- Ownership of local regulatory and financial compliance. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.
- Required to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed payment timelines.
- Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval relatedinteractions. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.
- Contribute or lead initiatives and projects adding value to the business, as appropriate/required.
- Contributes strongly to COM team and other Country Operations roles knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.
- Contributes to COM team knowledge by acting as buddy/mentor and sharing best practices as appropriate/required.

**Core competencies**:

- Expertise of core clinical systems, tools and metrics
- Excellent verbal and written influrencing and training/mentoring skills, in local language and English
- Strong coordination and organizational skills
- Skilled knowledge of budget and contract negotiations, local regulatory environment and submission and approval processes, and understanding of how these impact study start-up.
- Ability to indirectly influence investigators, vendors, external partners and country managers to address and resolve issues, with mínimal support from the Sr.COM or manager.
- Ability to make decisions independently with limited oversight from Sr.COM or manager.
- Requires strong understanding of local regulatory environment
- Ability to proactively develop risk management and mitigation plans in the country and resolve issues locally.
- Ability to lead a team of CTCs as applicable.

**Behavioural Competency Expectations**:

- Problem solving is essential to this position. Requires the ability to pro-actively identify issues and risks, analyse root cause, and propose solutions to problems and escalate to management as applicable. Specific examples of common problems include:

- 1) Issues in budget / CTRA negotiations
- 2) Quality and compliance issues
- 3) Regulatory and legal issues
- 4) issues related to functional area deliverables that could jeopardize protocol milestones.
- Effective and efficient time management, organizational and interpersonal skills, conflict management and problem-solving skills.
- High sense of accountability and urgency in order to properly prioritize deliverables
- Strong communication, leadership, and neg



  • São Paulo, Brasil ICON Plc Tempo inteiro

    Manager, Clinical Operations - Home Based - São Paulo / Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a...

  • Manager, Clinical Operations

    4 semanas atrás


    São Paulo, São Paulo, Brasil ICON Plc Tempo inteiro

    Manager, Clinical Operations - Home Based - São Paulo / BrazilICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Manager,...


  • Sao Paulo, Brasil MSD Tempo inteiro

    **Job Description**: Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. This role is accountable for performance and...


  • Sao Paulo, Brasil MSD Tempo inteiro

    This role is accountable for performance and compliance for assigned protocols in a country in compliance and regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally. The person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and...

  • Manager, Clinical Operations

    2 semanas atrás


    São Paulo, Brasil ICON Plc Tempo inteiro

    Manager, Clinical Operations - Remote - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development At ICON, it’s our people that set us apart. Our...


  • São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    Manager, Clinical Operations - Remote - BrazilICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentAt ICON, it's our people that set us apart.Our diverse...


  • São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$1.092.000 - R$1.365.000

    Job Title: Regional Clinical Operations LeaderWe are seeking a highly skilled Regional Clinical Operations Leader to lead regional clinical operations teams and ensure the successful delivery of clinical studies in the region.Key Responsibilities:Lead regional clinical operations teams effectively, ensuring effective decision-making and resolving issues...

  • Manager Clinical Operations

    1 semana atrás


    Sao Paulo, Brasil PPD Tempo inteiro

    PPD mission is enabling our customers to make the world healthier, cleaner and safer. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our...


  • São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$90.000 - US$120.000

    Clinical Operations Manager JobWe are seeking a skilled Clinical Operations Manager to join our team. This is an exciting opportunity for someone who wants to take on a challenging role and make a real impact in the field of clinical trials.Job Description:Accountable for study planning, start-up activities, and activation deliverables of assigned projects...


  • São Paulo, São Paulo, Brasil beBeeOperations Tempo inteiro R$138.656 - R$211.429

    Job Title:Operational Management ProfessionalAbout the Role:We are seeking a highly skilled professional to oversee the execution of clinical trials, ensuring they are conducted efficiently, on time, and in compliance with regulatory requirements.Manage a local team effectively, maximising resource use to deliver operational, quality, and fiscal targets...