Senior Neuropsychology Researcher: Alzheimer's Disease Clinical Trials

hace 4 semanas


Bogotá, Bogotá D.E., Colombia Igc Pharma Sas A tiempo completo

Career Opportunities at IGC Pharma SAS: Transforming Alzheimer's Research



Job Summary



Igc Pharma SAS, a subsidiary of a leading NYSE-listed pharmaceutical company, is seeking a highly skilled Senior Neuropsychology Researcher to join our team in Bogota. The successful candidate will play a pivotal role in the Alzheimer's disease clinical trials, driving innovative research and advancing our understanding of cognitive function.



About the Role



In this exciting position, you will oversee cognitive assessments, interpret neuropsychological test results, and contribute to the overall study design. You will work closely with researchers, neurologists, and clinical teams to ensure accurate evaluation of participants' cognitive function and monitor the impact of treatments over time. Key responsibilities include:





  • Design and refine cognitive testing protocols for Alzheimer's disease trials, ensuring tests are aligned with the objectives of the study.

  • Collaborate with clinical trial teams to monitor and assess cognitive outcomes over the course of the study.

  • Provide guidance in the selection of neuropsychological tests and the interpretation of cognitive data.

  • Participate in meetings with study investigators and trial teams to train them on neuropsychological tests.

  • Stay informed on the latest research and developments in Alzheimer's disease, cognitive testing, and neuropsychology.



Requirements



To be successful in this role, you will need:





  • A Master's degree in clinical psychology or Neuropsychology from an accredited program.

  • 2-3 years of experience conducting neuropsychological assessments, preferably in clinical research or with patients with neurodegenerative disorders.

  • Experience with Alzheimer's disease or other dementias is highly preferred.

  • Proficiency in a range of neuropsychological tests, including those commonly used for cognitive assessments in Alzheimer's disease research (e.g., ADAS-Cog, MMSE, MoCA).

  • Strong analytical skills and experience interpreting cognitive data in a clinical trial context.

  • Strong written and verbal communication skills in English.



Preferred Qualifications



Prior experience in clinical trials, particularly in the evaluation of cognitive function in neurodegenerative disease populations. Knowledge of regulatory standards for clinical trials, including Good Clinical Practice (GCP), is also an advantage.



What We Offer



Igc Pharma SAS offers a competitive salary, ranging from $80,000 to $110,000 per annum, depending on experience. Additionally, we provide excellent benefits, including travel opportunities to the U.S., training programs, and a dynamic work environment. Our company culture values diversity, teamwork, and continuous learning, making us an exciting and supportive workplace.



Location



This position is based in Bogota, Colombia. It is essential to have a valid U.S. Visa or be in the process of obtaining one.



Are You the Right Fit?



Are you a highly talented, collaborative, intelligent, compassionate, committed, well-traveled, self-driven individual with leadership qualities, a passion for working in healthcare, and a calling to help make lives better?



Please submit your application, including your resume and a cover letter, to [insert contact information]. We look forward to hearing from you.



Salary Estimate



The estimated annual salary for this position is $90,000, based on the national average salary for neuropsychology researchers in Colombia.



  • Bogotá, Bogotá D.E., Colombia Clínica Colombia Es A tiempo completo

    Regulatory Affairs Specialist Clinical TrialsAbout the CompanyIGC Pharma SAS is a subsidiary of a U.S. start-up clinical-stage pharmaceutical company based in New York, specializing in preventing and managing Alzheimer's and other CNS diseases. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the successful planning and...


  • Bogotá, Bogotá D.E., Colombia Igc Pharma Sas A tiempo completo

    Igc Pharma Sas Job Description:Company Overview:Igc Pharma Sas is a subsidiary of an NYSE-listed U.S. start-up development-stage pharmaceutical company that focuses on preventing and managing Alzheimer's and other CNS diseases. We also develop, manufacture, and over-the-counter market products for women's health.Job Description:We are seeking a highly...


  • Bogotá, Bogotá D.E., Colombia Icon A tiempo completo

    About the Role: We are seeking a Clinical Trials Administrator to support the coordination and administration of clinical trials at ICON. The successful candidate will assist in maintaining and organizing clinical trial documentation, ensuring compliance with protocols and regulatory requirements.Key Responsibilities:Assist in the coordination and...


  • Bogotá, Bogotá D.E., Colombia Eli Lilly and Company A tiempo completo

    At Eli Lilly and Company, we strive to make a meaningful difference in the lives of people around the world. Our commitment to innovation and excellence drives us to discover and develop life-changing medicines that improve the understanding and management of disease.Job Summary:We are seeking a highly skilled and experienced Clinical Research Physician to...


  • Bogotá, Bogotá D.E., Colombia Clínica Colombia ES A tiempo completo

    About the PositionClínica Colombia ES is seeking a highly skilled Regulatory Affairs Specialist to join our team in Bogota, Colombia. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the successful planning and execution of clinical trials and the regulatory approval of new drugs.Key Responsibilities:Regulatory Document...


  • Bogotá, Bogotá D.E., Colombia CDS Fortrea Inc. A tiempo completo

    OverviewCDS Fortrea Inc. is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.SalaryThe estimated salary for this position is $85,000 - $110,000 per year.Job DescriptionThis Senior Clinical Trials Coordinator role involves serving as the primary contact for project teams and...


  • Bogotá, Bogotá D.E., Colombia BOG Fortrea Colombia Ltda. A tiempo completo

    About Bog Fortrea Colombia Ltda.As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, our company provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20...


  • Bogotá, Bogotá D.E., Colombia Lilly A tiempo completo

    We are seeking a highly skilled Medical Affairs Director Alzheimer Disease Expert to join our team at Lilly. This role is a critical member of the medical affairs team, responsible for providing expert medical support to all aspects of the local business.Key Responsibilities:Provide expert medical support to all aspects of the local business.Develop and...


  • Bogotá, Bogotá D.E., Colombia Psi Cro A tiempo completo

    **Job Summary:**Psi Cro is a leading Contract Research Organization (CRO) seeking an experienced Clinical Trials Data Programmer to join our team. As a key member of our statistical programming team, you will be responsible for developing and maintaining high-quality data sets, programs, and documentation for global clinical trials.**Responsibilities:Develop...


  • Bogotá, Bogotá D.E., Colombia PSI A tiempo completo

    Job Title: Clinical Trials Regional Project LeadThis exciting opportunity is within PSI, a leading organization in the healthcare industry.Job DescriptionAs a Clinical Trials Regional Project Lead, you will be responsible for coordinating activities of project teams, ensuring milestones are met, and maintaining consistency of Clinical Operations processes...


  • Bogotá, Bogotá D.E., Colombia IQVIA A tiempo completo

    Job OverviewAs a Clinical Trials Operations Lead at IQVIA, you will be responsible for providing leadership of the centralized monitoring team to achieve the delivery of project objectives to the sponsor's satisfaction. You will work in partnership with project and clinical lead, and in collaboration with other functional teams, to optimize speed, quality,...


  • Bogotá, Bogotá D.E., Colombia Msd A tiempo completo

    At MSD, we're driven by a passion to innovate for life, bringing forward medicines and vaccines for many of the world's most challenging diseases.We're looking for a seasoned Senior Clinical Data Management Specialist to join our team, who will play a vital role in ensuring the quality and consistency of our data management deliverables.Key...


  • Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    About the Job:The Clinical Trials Coordinator will provide administrative and technical support to the project team. This includes ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document.Main Responsibilities:Coordinate, oversee, and complete functions on assigned trial activities as detailed...


  • Bogotá, Bogotá D.E., Colombia Psi Cro A tiempo completo

    Job DescriptionAs a Statistical Programmer at Psi Cro, you will contribute to statistical programming activities related to global clinical trials. You will work closely with international teams of statisticians, programmers, and data managers, programming data sets and summaries.Duties and ResponsibilitiesDevelop analysis data sets structureDevelop program...


  • Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job Title: Senior Clinical Research AssociateJob Summary:The Senior Clinical Research Associate will be responsible for managing and monitoring clinical research studies in a country, ensuring compliance with ICH/GCP and country regulations. The role will involve developing and expanding the territory for clinical research, finding and developing new sites,...


  • Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job Title: Principal Clinical Data ManagerJob Summary: We are seeking a highly skilled and experienced Principal Clinical Data Manager to join our team at MSD. The successful candidate will be responsible for ensuring the quality and consistency of clinical data management deliverables, providing technical guidance and design-specific recommendations, and...

  • SAS Programmer I

    hace 3 semanas


    Bogotá, Bogotá D.E., Colombia Psi CRO Ag A tiempo completo

    We are a dynamic, global company that cares for our staff, clients, partners, and the quality of work we do. With over 2,700 driven individuals, we work on the frontline of medical science, changing lives and bringing new medicines to those who need them.Job OverviewAs a SAS Programmer I at Psi CRO Ag, you will contribute to statistical programming...


  • Bogotá, Bogotá D.E., Colombia PSI A tiempo completo

    Job Title: Clinical Trials Regional Project LeadJob Summary:We are seeking a highly skilled Clinical Trials Regional Project Lead to join our team at PSI. As a key member of our Clinical Operations department, you will be responsible for coordinating project activities, ensuring milestones are met, and maintaining consistency of Clinical Operations processes...


  • Bogotá, Bogotá D.E., Colombia PSI A tiempo completo

    About this role:As a Clinical Trials Regional Project Lead at PSI, you will play a key role in coordinating project teams and ensuring milestones are met while maintaining consistency of Clinical Operations processes across regions.Key responsibilities:Coordinate project team work and supervise clinical project team members' performance.Implement and manage...


  • Bogotá, Bogotá D.E., Colombia Eli Lilly and Company A tiempo completo

    We are seeking a highly skilled Medical Director to lead our Alzheimer disease therapeutic area team. As a key member of our medical affairs team, you will be responsible for providing expert medical support to all aspects of our business, enhancing customer experience and addressing unmet needs of the medical scientific community.Key...