What Data Managers Jobs are in Kenya?
Showing 25 Data Managers jobs in Kenya
Pharmaceutical Data Manager (Remote)
51100 Kakamega / Remote
Placements24
Posted 20 days ago
Job Viewed
Job Description
About the Role Our client, a dynamic pharmaceutical company at the forefront of medical innovation, is seeking a meticulous and experienced Pharmaceutical Data Manager to join their fully remote team. This position is integral to the integrity and reliability of clinical trial data, ensuring that all collected information is accurate, complete, and compliant with regulatory standards. Working from your home office, you will manage the setup, validation, and maintenance of clinical databases, collaborating closely with biostatisticians, clinical research associates, and site personnel. Our client is committed to providing a supportive and flexible remote work environment, equipping you with the necessary tools and resources to excel. This is an outstanding opportunity for a detail-oriented professional to play a crucial role in drug development while benefiting from a remote-first career. Key Responsibilities
- Oversee the design, development, validation, and maintenance of clinical trial databases using EDC (Electronic Data Capture) systems.
- Develop Case Report Forms (CRFs) and edit checks to ensure data quality and consistency.
- Manage data cleaning activities, including resolving data discrepancies and queries with clinical sites and study teams.
- Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company SOPs throughout the data management lifecycle.
- Develop and execute data management plans (DMPs).
- Collaborate with biostatisticians to ensure timely database lock and report generation.
- Contribute to the selection and implementation of new data management technologies and tools.
- Train study team members on data entry and data management procedures.
- Prepare data management status reports for project teams and management.
- Bachelor's degree in a relevant field such as Computer Science, Life Sciences, Statistics, or Health Informatics.
- Minimum of 4 years of experience in clinical data management within the pharmaceutical or biotechnology industry.
- Proficiency with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC).
- Strong understanding of clinical trial processes, GCP, and regulatory data management requirements.
- Excellent understanding of database design principles and data validation techniques.
- Exceptional attention to detail and organizational skills.
- Effective communication and interpersonal skills, crucial for remote collaboration.
- Ability to manage multiple tasks and priorities effectively in a remote work setting.
- Competitive salary and potential for performance incentives.
- Comprehensive health, dental, and vision insurance plans.
- Generous paid time off and company holidays.
- Retirement savings plan with employer matching.
- Home office stipend and remote work support.
- Opportunities for professional development and continuing education.
- Flexible remote working arrangements.
- Engaging role in advancing drug development pipelines.
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0
Clinical Data Manager - Remote
40100 Ongata Rongai / Remote
Placements24
Posted 20 days ago
Job Viewed
Job Description
About the Role Our client, a leading clinical research organization (CRO) dedicated to advancing pharmaceutical and biotechnological innovations, is seeking an experienced Clinical Data Manager for a fully remote position. This role is vital in ensuring the accuracy, completeness, and consistency of clinical trial data collected across global study sites. The Clinical Data Manager will be responsible for managing all aspects of clinical data collection, validation, and database lock, adhering to strict regulatory standards and company SOPs. You will work closely with clinical teams, statisticians, and programmers to develop data management plans, design data collection tools, and oversee the clinical database build and maintenance. As a fully remote role, you will benefit from a flexible work environment while collaborating seamlessly with international teams using advanced digital communication and project management tools. This is an excellent opportunity to contribute to critical drug development programs and enhance patient safety from your home office, based in **Kenya**. We champion a culture of quality, efficiency, and continuous improvement.
Key Responsibilities
Key Responsibilities
- Oversee and manage clinical data management activities throughout the clinical trial lifecycle.
- Develop Data Management Plans (DMPs) in accordance with study protocols and regulatory requirements.
- Design, build, test, and maintain clinical databases using EDC systems (e.g., Medidata Rave, Oracle Clinical).
- Develop and execute data validation plans, including edit checks and manual data review strategies.
- Manage data query processes to resolve data discrepancies and ensure data accuracy and completeness.
- Oversee the cleaning and reconciliation of data from various sources.
- Lead database lock activities and ensure all data is finalized according to specifications.
- Collaborate with biostatisticians, clinical programmers, and study teams to ensure data quality and timely delivery.
- Ensure compliance with ICH-GCP, HIPAA, and other relevant regulatory guidelines.
- Participate in study team meetings and provide input on data management aspects.
- Bachelor's degree in a scientific, health-related, or IT field.
- Minimum of 4 years of experience in clinical data management within the pharmaceutical, biotech, or CRO industry.
- Proven experience with Electronic Data Capture (EDC) systems and clinical data management software.
- Strong understanding of clinical trial processes, database design, data validation, and data query management.
- Knowledge of ICH-GCP guidelines and regulatory requirements related to clinical data.
- Excellent organizational, problem-solving, and analytical skills.
- Strong written and verbal communication abilities, with the capacity to communicate technical information clearly.
- Ability to work independently, manage multiple priorities, and meet project deadlines in a remote setting.
- Proficiency in standard office software (e.g., Microsoft Office Suite).
- Must be based in **Kenya** and eligible to work remotely full-time.
- Competitive salary commensurate with experience.
- Comprehensive health, dental, and vision insurance coverage.
- Generous paid time off and holidays.
- Opportunities for professional development and career advancement.
- Access to cutting-edge data management technologies and training.
- Flexible remote work schedule that promotes a healthy work-life balance.
- Be part of a dynamic team contributing to significant medical advancements.
- Retirement savings plan.
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1
Subsurface Data Manager (Remote)
Posted 10 days ago
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Job Description
About the Role Our client, a leading entity in the Oil & Gas sector, is seeking a highly organized and technically proficient Subsurface Data Manager to join their fully remote workforce. This critical role is responsible for overseeing the collection, organization, quality control, and accessibility of all subsurface data, including seismic, well logs, core data, and production information. You will implement and maintain robust data management systems and workflows to ensure data integrity and support geological, geophysical, and engineering teams in their decision-making processes. As a remote-first organization, we are dedicated to providing a seamless and collaborative digital environment for all team members. This is an excellent opportunity to shape data governance strategies and enhance data utilization in a globally significant industry. Key Responsibilities
- Develop and implement comprehensive data management strategies for subsurface data.
- Establish and enforce data quality control procedures and standards.
- Oversee the acquisition, cataloging, and archiving of all relevant subsurface datasets.
- Manage and maintain subsurface databases and data management systems.
- Ensure data security, integrity, and accessibility for authorized users.
- Collaborate with IT and subsurface teams to optimize data infrastructure and tools.
- Provide training and support to users on data management systems and best practices.
- Generate reports on data status, quality metrics, and system performance.
- Stay current with industry best practices and emerging technologies in subsurface data management.
- Bachelor's degree in Geoscience, Computer Science, Information Management, or a related field.
- Minimum of 7 years of experience in subsurface data management within the Oil & Gas industry.
- Proven experience with industry-standard data management software and databases (e.g., Petra, GeoScout, SQL).
- Deep understanding of various subsurface data types (seismic, well logs, core, production, etc.).
- Strong knowledge of data governance, quality control, and data lifecycle management principles.
- Excellent analytical, problem-solving, and organizational skills.
- Demonstrated ability to work independently and manage projects effectively in a remote setting.
- Strong communication and interpersonal skills for effective remote collaboration.
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2
Job Description
About the Role Our client, a rapidly growing pharmaceutical research organization, is seeking a diligent and detail-oriented Clinical Data Manager to join their team. This hybrid role offers a blend of remote flexibility and in-office collaboration, based in **Embu, Kenya**. You will be responsible for overseeing the collection, management, and quality control of clinical trial data, ensuring its accuracy, completeness, and compliance with regulatory standards. Your work is crucial for the integrity and success of clinical studies aimed at developing new pharmaceutical therapies. This position demands a strong understanding of data management principles, clinical trial processes, and regulatory requirements within the **pharmaceutical industry**. Key Responsibilities
- Develop and maintain Clinical Data Management Plans (CDMPs) in accordance with study protocols and regulatory guidelines.
- Design and build Electronic Data Capture (EDC) systems, including Case Report Forms (CRFs) and edit checks.
- Oversee data entry, data cleaning, and query resolution processes to ensure data quality and integrity.
- Perform data validation checks and identify discrepancies, working with study sites to resolve them promptly.
- Manage database lock activities upon study completion, ensuring all data is accurate and finalized.
- Collaborate with Biostatisticians, Clinical Research Associates (CRAs), and other study team members to define data management requirements and resolve data issues.
- Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulatory requirements.
- Contribute to the development and implementation of data management standards and best practices.
- Train and provide guidance to data management personnel and site staff as needed.
- Bachelor's degree in Computer Science, Statistics, Life Sciences, or a related field.
- Minimum of 3 years of experience in clinical data management within the **pharmaceutical industry** or a CRO.
- Proficiency with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical) and data management software.
- Solid understanding of clinical trial processes, CDISC standards, and regulatory requirements (GCP, ICH).
- Strong analytical and problem-solving skills with meticulous attention to detail.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively.
- Experience in database design, data validation, and query management.
- Ability to manage multiple projects and meet deadlines in a dynamic environment.
- Competitive salary and performance incentives.
- Comprehensive health insurance coverage.
- Paid time off and holidays.
- Opportunities for professional growth and development in data management.
- Exposure to diverse clinical trial projects.
- Hybrid work model offering flexibility.
- Supportive team environment committed to quality research.
- Contribution to advancing pharmaceutical research and patient care.
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3
Data Manager (Clinical Trials - Remote)
41100 Garissa / Remote
Placements24
Posted 17 days ago
Job Viewed
Job Description
About the Role Our client, a prominent global **pharmaceutical** research organization, is seeking an experienced Data Manager to join their fully **remote** clinical trials team. This role is critical for ensuring the accuracy, completeness, and integrity of clinical trial data across all phases of research. You will be responsible for the design, development, and management of clinical databases, implementation of data management plans, and ensuring adherence to Good Clinical Practice (GCP) and regulatory standards. The ideal candidate is highly organized, possesses strong technical skills in clinical data management systems, and thrives in an independent, collaborative remote work environment. Your expertise will directly contribute to the successful execution of clinical studies and the advancement of new therapies. Key Responsibilities
- Oversee the design, development, validation, and maintenance of clinical databases using EDC systems (e.g., Medidata Rave, Oracle Clinical).
- Develop and implement comprehensive data management plans (DMPs) in collaboration with study teams.
- Define data collection standards, edit checks, and data validation procedures to ensure data quality and integrity.
- Manage data cleaning activities, including query generation, resolution, and trending, to ensure timely database lock.
- Perform quality control checks on data management deliverables and study conduct.
- Train site personnel and internal team members on data entry procedures and EDC system usage.
- Collaborate with biostatisticians, clinical programmers, and clinical operations personnel to meet study timelines and data requirements.
- Ensure compliance with GCP, regulatory requirements (FDA, EMA), and company SOPs throughout the data management lifecycle.
- Contribute to the development and improvement of data management processes and standards.
- Participate in study team meetings and provide regular updates on data management status.
- Bachelor's degree in a scientific, technical, or healthcare-related field. Master's degree is a plus.
- Minimum of 5 years of experience in clinical data management within the **pharmaceutical**, biotechnology, or CRO industry.
- Proven experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva Vault EDC).
- Strong understanding of clinical trial processes, GCP guidelines, and regulatory requirements (e.g., FDA 21 CFR Part 11).
- Proficiency in database design, data validation, query management, and database lock procedures.
- Excellent analytical and problem-solving skills with meticulous attention to detail.
- Strong written and verbal communication skills, with the ability to effectively interact with study teams.
- Demonstrated ability to work independently, manage multiple projects, and meet strict deadlines in a remote setting.
- Proficiency in standard office software and data management tools.
- Experience with data standards such as CDISC (SDTM, ADaM) is highly desirable.
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4
Senior Clinical Data Manager
Posted 20 days ago
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Job Description
About the Role Our client, a cutting-edge pharmaceutical research organization, is looking for an experienced Senior Clinical Data Manager to join their fully remote clinical operations team. This role is instrumental in ensuring the integrity, accuracy, and quality of clinical trial data across all phases of drug development. The ideal candidate will have a strong understanding of clinical data management systems, database design, data validation, and regulatory compliance within a remote setting. This is a fantastic opportunity to contribute to vital clinical research from your preferred location within Nyeri, Nyeri, KE , helping to bring life-changing therapies to patients faster. Our client is committed to a remote-first approach, providing the necessary technology and collaborative platforms for success. Key Responsibilities
- Oversee the end-to-end clinical data management process for assigned clinical trials.
- Develop and maintain clinical databases, including database design, build, and testing.
- Create and execute data validation plans, specifications, and edit checks.
- Manage data cleaning activities, resolving data discrepancies in collaboration with study sites and project teams.
- Ensure compliance with Good Clinical Practice (GCP), relevant regulatory guidelines (e.g., FDA, EMA), and internal SOPs.
- Generate data management reports and status updates for project teams and management.
- Lead data management activities during study startup, maintenance, and close-out phases.
- Provide expertise and guidance on data management best practices to internal and external stakeholders.
- Contribute to the continuous improvement of data management processes and systems.
- Bachelor's degree in a scientific, medical, or related field. A Master's degree is preferred.
- Minimum of 6 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry.
- Proven experience with clinical data management systems (CDMS) such as Medidata Rave, Oracle Clinical, or similar.
- Strong understanding of database design principles, UAT, and data validation strategies.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical data.
- Experience in managing data for various trial phases (Phase I-IV).
- Excellent analytical, organizational, and problem-solving skills.
- Effective communication and collaboration skills, particularly in a remote team environment.
- Must be legally authorized to work in Nyeri, Nyeri, KE and have a reliable internet connection for remote work.
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5
Job Description
About the Role Our client, a prominent force in the pharmaceutical industry, is actively searching for an experienced Lead Clinical Data Manager to spearhead their data management operations. This is a fully remote position, offering a unique opportunity to contribute to groundbreaking clinical trials from the comfort of your home, regardless of your location. The successful candidate will be instrumental in ensuring the accuracy, integrity, and quality of clinical trial data, which is paramount to regulatory approval and the development of life-saving medications. This role demands a strategic thinker with a deep understanding of data management best practices and regulatory compliance. The ideal candidate will possess strong leadership capabilities and a proven ability to manage complex data sets across multiple studies. As a remote-first role, you will be empowered with the autonomy to manage your workload effectively while collaborating closely with global teams. This position is critical in upholding the highest standards of data integrity, directly impacting the success of our client's research and development pipeline. We are committed to fostering a remote work environment that promotes collaboration, innovation, and professional growth. The insights derived from the data you manage will pave the way for future therapeutic breakthroughs, making this a truly impactful role in the pharmaceutical landscape. You will be a key contributor to ensuring that our client's clinical research meets rigorous global standards. Your dedication to data quality will directly support the development of new medicines. Key Responsibilities
- Oversee all aspects of clinical data management for multiple complex clinical trials, ensuring adherence to study protocols and regulatory requirements (e.g., ICH-GCP, FDA, EMA).
- Develop and implement data management plans (DMPs), including data collection, validation, query management, and database lock procedures.
- Design and review case report forms (CRFs), electronic data capture (EDC) systems, and data validation specifications.
- Lead and mentor a team of clinical data managers, providing guidance and oversight on study activities and professional development.
- Ensure the quality and integrity of clinical databases through rigorous validation checks and reconciliation processes.
- Collaborate closely with principal investigators, clinical research associates (CRAs), biostatisticians, and programming teams to resolve data discrepancies and ensure timely database lock.
- Manage third-party data vendors and ensure their performance meets project and company standards.
- Contribute to the development and improvement of data management SOPs, processes, and systems.
- Stay updated on industry trends, best practices, and regulatory guidelines in clinical data management.
- Participate in data review meetings and present data management status updates to project teams and stakeholders.
- Bachelor's or Master's degree in a relevant scientific or technical field (e.g., Health Informatics, Computer Science, Statistics, Life Sciences).
- A minimum of 7-10 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry.
- Proven experience leading data management activities for global clinical trials, across various phases (I-IV).
- In-depth knowledge of EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva) and data management best practices.
- Strong understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Excellent leadership, project management, and organizational skills.
- Superior analytical and problem-solving abilities, with meticulous attention to detail.
- Exceptional communication and interpersonal skills, with the ability to effectively collaborate with diverse, remote teams.
- Ability to work independently, manage priorities, and meet deadlines in a fast-paced, remote environment.
- Experience with data standards such as CDISC (SDTM, ADaM) is highly preferred.
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6
Remote Pharmaceutical Clinical Data Manager
30100 Eldoret / Remote
Placements24
Posted 20 days ago
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Job Description
About the Role Our client, a globally recognized pharmaceutical organization, is seeking a highly skilled and dedicated Remote Pharmaceutical Clinical Data Manager to join their expanding clinical operations team. This fully remote position empowers professionals to contribute significantly to clinical trial data management from the comfort of their home office. The Clinical Data Manager will be responsible for the end-to-end management of clinical trial data, ensuring its accuracy, completeness, and integrity in compliance with regulatory standards. This role is crucial for supporting the successful execution of clinical trials and enabling the timely analysis of trial results. We are looking for a meticulous individual with a strong understanding of clinical trial processes and data management best practices, eager to contribute to life-saving research in a flexible, remote-first capacity. Key Responsibilities
- Oversee the design, development, and implementation of clinical databases (EDC systems).
- Develop and maintain Data Management Plans (DMPs) for clinical trials.
- Define data collection requirements and create Case Report Forms (CRFs) and eCRFs.
- Manage data cleaning activities, including query generation, reconciliation, and resolution.
- Ensure compliance with ICH-GCP guidelines, HIPAA, and other relevant regulatory requirements.
- Perform data validation checks and quality control procedures.
- Collaborate with clinical research associates (CRAs), study statisticians, and investigators.
- Manage external data integrations (e.g., labs, imaging).
- Prepare database lock packages and ensure data archival.
- Contribute to the continuous improvement of data management processes and standards.
- Train and mentor junior data management personnel as needed.
- Bachelor's degree in a relevant scientific or healthcare field (e.g., Nursing, Pharmacy, Life Sciences, IT).
- Minimum of 5 years of experience in clinical data management within the pharmaceutical or CRO industry.
- Extensive experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC).
- Strong understanding of clinical trial processes, regulatory guidelines (ICH-GCP), and data standards (CDISC).
- Proficiency in database design, data validation, and data cleaning techniques.
- Excellent organizational, problem-solving, and analytical skills.
- Ability to manage multiple projects simultaneously and meet deadlines.
- Exceptional written and verbal communication skills.
- Proven ability to work independently and effectively in a remote team environment.
- Detail-oriented with a strong commitment to data quality and integrity.
- A competitive annual salary of KSh , reflective of your expertise.
- A fully remote work setup, providing ultimate flexibility.
- Comprehensive health, dental, and vision insurance plans.
- Generous allowance for paid time off and holidays.
- Opportunities for professional development and certifications in clinical data management.
- Access to industry-leading data management software and tools.
- A collaborative and supportive remote team culture.
- Reimbursement for home office equipment and internet services.
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7
Senior Pharmaceutical Clinical Data Manager
00200 Ongata Rongai / Remote
Placements24
Posted 16 days ago
Job Viewed
Job Description
About the Role Our client, a leading pharmaceutical company dedicated to advancing medical treatments, is seeking an experienced Senior Pharmaceutical Clinical Data Manager to join their dynamic, fully remote team. This essential role will oversee the collection, management, and quality assurance of clinical trial data, ensuring its accuracy, integrity, and compliance with regulatory standards. While the position is remote, it will contribute to global clinical trial efforts supporting research relevant to **Ongata Rongai, Kajiado, KE**. The ideal candidate will possess a strong understanding of clinical data management systems, EDC platforms, and regulatory requirements such as ICH-GCP. You will play a crucial part in enabling robust clinical decision-making and regulatory submissions through meticulous data handling. Join a collaborative and innovative environment focused on bringing life-changing therapies to market, all within a flexible, remote-first setup. Key Responsibilities
- Oversee the design, development, and implementation of clinical databases, including eCRF design and UAT.
- Develop and execute Data Management Plans (DMPs) in collaboration with clinical study teams.
- Manage data cleaning activities, including query generation, resolution, and reconciliation with external data sources.
- Ensure data accuracy, completeness, and consistency in compliance with study protocols and SOPs.
- Oversee the setup and validation of Electronic Data Capture (EDC) systems.
- Participate in the development and execution of risk-based data management strategies.
- Generate and review data management metrics, status reports, and audit trails.
- Ensure compliance with all applicable regulatory requirements, including ICH-GCP, FDA, and EMA guidelines.
- Collaborate with statisticians, programmers, clinical operations, and other study team members to ensure data quality and timely database lock.
- Contribute to the continuous improvement of data management processes and systems.
- Bachelor's degree in a scientific, technical, or healthcare-related field. Master’s degree preferred.
- A minimum of 5-7 years of experience in clinical data management within the pharmaceutical or biotech industry.
- Proven experience with EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC) and data cleaning/query management.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical data management.
- Experience in database design, UAT, and data validation processes.
- Strong understanding of clinical trial processes and terminology.
- Excellent analytical, problem-solving, and organizational skills.
- Strong written and verbal communication skills, with the ability to clearly articulate data issues and resolutions.
- Ability to work independently, manage multiple priorities, and meet strict deadlines in a remote environment.
- Proficiency in data analysis tools and reporting capabilities is a plus.
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8
Remote Clinical Data Manager - Pharmaceutical Trials
20100 Naivasha / Remote
Placements24
Posted 15 days ago
Job Viewed
Job Description
About the Role Our client, a trailblazing biopharmaceutical company dedicated to advancing novel therapies, is actively seeking a highly skilled and detail-oriented Remote Clinical Data Manager to contribute to critical clinical trial operations. This fully remote position allows you to leverage your expertise in data management from anywhere, playing a crucial role in ensuring the integrity, accuracy, and timeliness of clinical trial data that underpins life-changing drug development. You will be responsible for overseeing the entire data management lifecycle, from database design and setup to data cleaning, validation, and database lock. This role demands a strong understanding of clinical trial processes, regulatory requirements, and data management best practices. As a remote team member, you will collaborate closely with clinical operations, biostatistics, and programming teams to ensure the successful execution of studies and the delivery of high-quality data for regulatory submissions. The opportunity to work remotely provides unparalleled flexibility while making a significant impact. Key Responsibilities
- Oversee the design, development, and validation of clinical databases (e.g., EDC systems) in accordance with study protocols and regulatory requirements.
- Develop and maintain clinical data management plans (CDMPs) and data validation plans (DVPs).
- Manage data entry, query generation, and resolution processes to ensure data accuracy and completeness.
- Perform data review and quality control checks throughout the study lifecycle.
- Collaborate with statisticians and programmers to define data analysis specifications and reporting requirements.
- Ensure compliance with GCP, ICH guidelines, and relevant data privacy regulations.
- Oversee the vendor management of clinical data management service providers.
- Lead database lock activities upon study completion, ensuring all data issues are resolved.
- Contribute to the continuous improvement of data management processes and standards.
- Train and mentor junior data management personnel as needed.
- Bachelor's degree in a scientific or technical field (e.g., Computer Science, Statistics, Life Sciences) or equivalent experience.
- Minimum of 6 years of experience in clinical data management within the pharmaceutical or biotechnology industry.
- Proven experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva Vault EDC).
- Strong understanding of clinical trial processes, drug development, and regulatory requirements (GCP, ICH).
- Experience in developing data management plans, validation checks, and standard operating procedures (SOPs).
- Excellent analytical and problem-solving skills, with a meticulous attention to detail.
- Proficiency in database programming or SQL is a plus.
- Strong communication and interpersonal skills, with the ability to work effectively in a remote, cross-functional team environment.
- Ability to manage multiple projects simultaneously and prioritize tasks effectively.
- Commitment to data integrity and patient safety.
- Highly competitive salary and potential for performance-based bonuses.
- Comprehensive medical, dental, and vision insurance plans.
- Generous retirement savings plan with employer contributions.
- Flexible work hours and a fully remote work environment.
- Opportunities for professional growth, including training and conference attendance.
- Collaborative and innovative work culture focused on scientific advancement.
- Work on groundbreaking clinical trials that have a direct impact on patient lives.
- State-of-the-art remote work infrastructure and support.
- Paid time off and holidays.
- The satisfaction of contributing to the development of new medicines from your home office.
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