About Company
Career.zycto champions the future of clinical research by empowering exceptional talent with unparalleled opportunities. For a Clinical Data Manager, this means direct access to pioneering projects, leveraging your expertise from the comfort of your remote workspace. We are dedicated to fostering environments where precision meets passion, ensuring every data point contributes meaningfully to global health advancements. Join a network that values your meticulous eye and drives significant impact in a flexible, supportive setting. Career.zycto is where your expertise finds its next challenge.
Job Description
Are you a highly meticulous and experienced Clinical Data Manager seeking a challenging remote opportunity within the dynamic realm of clinical research? Career.zycto is seeking a dedicated professional to join our network and contribute to groundbreaking studies that shape the future of medicine. In this fully remote role, you will play a critical part in managing clinical trial data, ensuring its integrity, accuracy, and compliance with regulatory standards. Your expertise will directly impact the reliability of study results, supporting critical decision-making processes and the advancement of new therapies.
We are looking for someone with a proactive approach to problem-solving, a deep understanding of data management principles, and a commitment to quality. This position offers the flexibility of remote work while keeping you closely connected to a collaborative team of experts. If you are passionate about data, thrive in a detail-oriented environment, and are eager to make a significant contribution to clinical development from anywhere in the UK, we encourage you to apply. This is an exceptional opportunity to enhance your career, work on diverse projects, and be part of an organization that truly values your contribution to scientific progress and patient well-being.
Key Responsibilities
- Develop and review Data Management Plans (DMPs), Case Report Forms (CRFs), and other study-specific documentation.
- Oversee the design, development, and validation of clinical trial databases (EDC systems).
- Perform data review, query generation, and resolution to ensure data accuracy and completeness.
- Implement and maintain data quality control procedures throughout the study lifecycle.
- Collaborate with cross-functional teams including clinical operations, biostatistics, and medical writing.
- Ensure adherence to Good Clinical Practice (GCP), regulatory requirements, and standard operating procedures (SOPs).
- Manage and reconcile external data (e.g., lab data, imaging data) with clinical database.
- Participate in the development and implementation of data management standards and processes.
- Prepare and present data management metrics and status reports to project teams.
- Support database lock activities and deliver clean datasets for statistical analysis.
Required Skills
- Minimum of 3 years of experience in Clinical Data Management within pharmaceutical, biotech, or CRO industries.
- Proficiency with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, InForm, Veeva Vault EDC).
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements (e.g., FDA, EMA).
- Strong understanding of clinical trial phases and data management lifecycle.
- Excellent analytical skills and attention to detail.
- Proven ability to work independently and as part of a remote team.
- Exceptional communication and interpersonal skills.
- Advanced proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
Preferred Qualifications
- Bachelor's degree or higher in a life science, health-related field, or computer science.
- Experience with SQL or other programming languages for data manipulation and reporting.
- Certification in Clinical Data Management (e.g., SCDM).
- Experience with CDISC standards (SDTM, ADaM, CDASH).
- Demonstrated experience in leading data management activities for complex studies.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and public holidays.
- Flexible remote work environment.
- Opportunities for professional development and continuous learning.
- Access to cutting-edge clinical research projects.
- Supportive and collaborative team culture.
- Contribution to impactful global health initiatives.
- Company-provided home office stipend or equipment.
How to Apply
Ready to make a significant impact from the comfort of your home? We invite you to apply for this exciting remote opportunity. Please click on the application link below to submit your resume and cover letter, detailing your relevant experience and why you are the ideal candidate for this role. We look forward to reviewing your application!
