Job Title:
eClinical Project Manager Location:
London, United Kingdom (Hybrid or Office-Based) Employment Type:
Contract - Outside IR35 Rate:
£350 - £400 p/d About the Role: BioTalent is excited to partner with a globally renowned CRO to find an experienced
eClinical Project Manager
to join their growing team in London. This role offers a fantastic opportunity for an accomplished professional to oversee and manage eClinical solutions, driving the delivery of cutting-edge technologies that enhance clinical trial outcomes. As the eClinical Project Manager, you will collaborate with internal and external stakeholders, ensuring the seamless implementation of eClinical systems, such as EDC, eCOA, CTMS, and other digital platforms, to optimize clinical trial efficiency and data quality. Key Responsibilities: Serve as the primary point of contact for clients, ensuring effective communication and collaboration throughout the project lifecycle. Oversee the planning, implementation, and delivery of eClinical solutions, ensuring projects are completed on time, within scope, and budget. Develop and manage project timelines, milestones, and deliverables, ensuring alignment with client expectations and organizational objectives. Collaborate with cross-functional teams, including IT, clinical operations, and data management, to address technical and operational challenges. Monitor project progress, identify risks, and implement mitigation strategies to ensure successful outcomes. Provide training and support to internal teams and external stakeholders on eClinical systems and workflows. Ensure compliance with regulatory requirements, industry standards (ICH-GCP), and company policies. Prepare and present project status reports, metrics, and updates to clients and senior management. Candidate Profile: This role is ideal for a proactive and detail-oriented professional with strong project management expertise and a passion for leveraging technology to improve clinical trial processes. Qualifications: Education:
Bachelor’s degree in Life Sciences, Computer Science, or a related field (advanced degree preferred). Experience:
Minimum of 3-5 years of project management experience within a CRO, pharmaceutical, or clinical technology environment, with a strong focus on eClinical systems. Proven track record of managing multiple eClinical projects (e.g., EDC, eCOA, CTMS) successfully. Familiarity with clinical trial processes, regulatory guidelines, and industry standards (e.g., FDA, EMA, ICH-GCP). Strong technical understanding of eClinical platforms and their integration within clinical trial workflows. Skills: Exceptional project management and organizational skills, with the ability to prioritize tasks and manage competing deadlines. Excellent communication and interpersonal skills, with the ability to build strong client relationships. Analytical and problem-solving mindset, with the ability to identify and resolve issues effectively. Proficiency in project management tools and methodologies (e.g., Agile, Waterfall, MS Project).
#J-18808-Ljbffr
eClinical Project Manager Location:
London, United Kingdom (Hybrid or Office-Based) Employment Type:
Contract - Outside IR35 Rate:
£350 - £400 p/d About the Role: BioTalent is excited to partner with a globally renowned CRO to find an experienced
eClinical Project Manager
to join their growing team in London. This role offers a fantastic opportunity for an accomplished professional to oversee and manage eClinical solutions, driving the delivery of cutting-edge technologies that enhance clinical trial outcomes. As the eClinical Project Manager, you will collaborate with internal and external stakeholders, ensuring the seamless implementation of eClinical systems, such as EDC, eCOA, CTMS, and other digital platforms, to optimize clinical trial efficiency and data quality. Key Responsibilities: Serve as the primary point of contact for clients, ensuring effective communication and collaboration throughout the project lifecycle. Oversee the planning, implementation, and delivery of eClinical solutions, ensuring projects are completed on time, within scope, and budget. Develop and manage project timelines, milestones, and deliverables, ensuring alignment with client expectations and organizational objectives. Collaborate with cross-functional teams, including IT, clinical operations, and data management, to address technical and operational challenges. Monitor project progress, identify risks, and implement mitigation strategies to ensure successful outcomes. Provide training and support to internal teams and external stakeholders on eClinical systems and workflows. Ensure compliance with regulatory requirements, industry standards (ICH-GCP), and company policies. Prepare and present project status reports, metrics, and updates to clients and senior management. Candidate Profile: This role is ideal for a proactive and detail-oriented professional with strong project management expertise and a passion for leveraging technology to improve clinical trial processes. Qualifications: Education:
Bachelor’s degree in Life Sciences, Computer Science, or a related field (advanced degree preferred). Experience:
Minimum of 3-5 years of project management experience within a CRO, pharmaceutical, or clinical technology environment, with a strong focus on eClinical systems. Proven track record of managing multiple eClinical projects (e.g., EDC, eCOA, CTMS) successfully. Familiarity with clinical trial processes, regulatory guidelines, and industry standards (e.g., FDA, EMA, ICH-GCP). Strong technical understanding of eClinical platforms and their integration within clinical trial workflows. Skills: Exceptional project management and organizational skills, with the ability to prioritize tasks and manage competing deadlines. Excellent communication and interpersonal skills, with the ability to build strong client relationships. Analytical and problem-solving mindset, with the ability to identify and resolve issues effectively. Proficiency in project management tools and methodologies (e.g., Agile, Waterfall, MS Project).
#J-18808-Ljbffr
