Updated: Yesterday Location: London, LND, United Kingdom Job ID: Summary Demonstrates process expertise and therapeutic area knowledge. Acts as a key scientific leader on projects. Collaborates with Medical and Scientific Management (MSM) team members as well as with functions outside to provide high-quality deliverables. Responsible for coordinating the functional team members and their activities for medical and scientific services, liaising with project leadership and the customer to ensure that the MSM deliverables (timelines, quality, productivity) are met. This role has overall accountability for the execution of the Medical Management strategy on the project. Job Responsibilities Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical monitoring, medical data review, eligibility review and other project specific medical services. Works with Medical Directors to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Works with customers to develop non-standard procedures and project plans. Performs regular and ad-hoc medical review of data listings and visualizations as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise. Provides advanced medical data review on various project level data as needed. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Identifies and escalates ongoing and newly developed study concerns such as at risk project deliverables and out of scope tasks to the project leads in a timely manner. Troubleshoots situations as needed. Acts as key scientific leader on customer partnership/portfolio/coalition level. Attends strategic meetings with customers. Leads Scientific Services team on a project and evaluates resourcing needs. Serves as respective area's Subject Matter Expert (SME) to ensure that project teams consistently operate in compliance with research principles and procedures. Provides scientific oversight and project/product development training to Company staff and project teams. Attends and presents at Trusted Process meetings and may participate in internal and external audits or inspections. Assists with responding to findings from audits or inspections. Contributes to general and project specific training. Assists Medical Director(s) on the review and development of training material and project level documents, including but not limited to clinical protocols, clinical study reports, abstract and manuscripts, presentations, investigator brochures, and various other internal and external documents and communications as needed. Develops, or oversees the development of, work orders and change orders for projects involving MSM. Contributes to Company business development activities by providing scientific input into data collection tools, data monitoring plans, requests for proposals (RFPs), as assigned. Acquires understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Provides strategic oversight and active contributions to the planning and development of medical monitoring and scientific services activities, as well as provides direction and oversight across all research projects, and other research related activities. Evaluates processes for improvement in efficiency and effectiveness and recommends changes; participates in process development and improvement of departmental functions. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Equity, Diversity, and Inclusion Statement Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Apr 24, 2026
Full time
Updated: Yesterday Location: London, LND, United Kingdom Job ID: Summary Demonstrates process expertise and therapeutic area knowledge. Acts as a key scientific leader on projects. Collaborates with Medical and Scientific Management (MSM) team members as well as with functions outside to provide high-quality deliverables. Responsible for coordinating the functional team members and their activities for medical and scientific services, liaising with project leadership and the customer to ensure that the MSM deliverables (timelines, quality, productivity) are met. This role has overall accountability for the execution of the Medical Management strategy on the project. Job Responsibilities Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical monitoring, medical data review, eligibility review and other project specific medical services. Works with Medical Directors to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Works with customers to develop non-standard procedures and project plans. Performs regular and ad-hoc medical review of data listings and visualizations as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise. Provides advanced medical data review on various project level data as needed. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Identifies and escalates ongoing and newly developed study concerns such as at risk project deliverables and out of scope tasks to the project leads in a timely manner. Troubleshoots situations as needed. Acts as key scientific leader on customer partnership/portfolio/coalition level. Attends strategic meetings with customers. Leads Scientific Services team on a project and evaluates resourcing needs. Serves as respective area's Subject Matter Expert (SME) to ensure that project teams consistently operate in compliance with research principles and procedures. Provides scientific oversight and project/product development training to Company staff and project teams. Attends and presents at Trusted Process meetings and may participate in internal and external audits or inspections. Assists with responding to findings from audits or inspections. Contributes to general and project specific training. Assists Medical Director(s) on the review and development of training material and project level documents, including but not limited to clinical protocols, clinical study reports, abstract and manuscripts, presentations, investigator brochures, and various other internal and external documents and communications as needed. Develops, or oversees the development of, work orders and change orders for projects involving MSM. Contributes to Company business development activities by providing scientific input into data collection tools, data monitoring plans, requests for proposals (RFPs), as assigned. Acquires understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Provides strategic oversight and active contributions to the planning and development of medical monitoring and scientific services activities, as well as provides direction and oversight across all research projects, and other research related activities. Evaluates processes for improvement in efficiency and effectiveness and recommends changes; participates in process development and improvement of departmental functions. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Equity, Diversity, and Inclusion Statement Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Medical Scientist (12 Month Fixed Term Contract- UK) Updated: April 13, 2026 Location: GBR-Remote Job ID: Responsibilities Work with the Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, Eligibility Review Plan); engage outside experts, consultants and advisors to coordinate necessary medical/scientific input. Perform regular and ad hoc medical reviews of data listings and visualisations; analyse the data to identify risks, patterns and trends, and support documentation of medical reviews. Author medical data queries, review query responses and approve query closure in association with the Medical Director. Assist the Medical Director with patient profile reviews, scientific reviews of study level data, protocol deviation reviews and the creation of Medical Review Summary reports when needed. Partner with Medical Directors for medical data review meetings and safety review meetings, including slide preparation. Manage project scope, objectives and quality of deliverables to ensure project specific milestones and timelines are met; serve as the primary interface between the internal team, customers and vendors in medical data review and eligibility review areas. Collaborate with study team members (Clinical Operations, Data Management, Drug Safety & Pharmacovigilance, Project Management) to identify risks related to data integrity and subject safety; promptly escalat e concerns to the project leads. Attend Trusted Process meetings and may participate in internal and external audits. Acquire a basic understanding of ongoing protocol designs, disease related terminology and pathology. Adhere to data privacy guidelines, ICH, GCP, enterprise policies, SOPs, work instructions, project plans and customer policies. Qualifications MD is required. Minimum two years of direct patient care experience post residency. Must be located in the UK; no sponsorship will be considered. Excellent time management skills to handle multiple tasks and meet deadlines in a highly regulated environment. A self starter comfortable with fluctuating timelines, changing scope and work demands. Ability to troubleshoot situations and determine when to escalation issues to leadership. Understanding of scientific principles to assure effective and high quality medical data analysis. Excellent written and oral communication skills. Strong computer skills: MS Office, spreadsheets, presentations. Preferred knowledge of drug development and proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and capability to work effectively in a cross functional team environment. Additional Information Tasks, duties and responsibilities listed above are not exhaustive. The Company may assign additional duties. Equivalent experience, skills or education will be considered. The Company will determine what constitutes an equivalent qualification. This description complies with all applicable legislation, including the EU Equality Directive and the Americans with Disabilities Act. Equal Opportunity Statement Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, age, religion, marital status, ethnicity, national origin, sex, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any portion of the application process, please contact: .
Apr 21, 2026
Full time
Medical Scientist (12 Month Fixed Term Contract- UK) Updated: April 13, 2026 Location: GBR-Remote Job ID: Responsibilities Work with the Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, Eligibility Review Plan); engage outside experts, consultants and advisors to coordinate necessary medical/scientific input. Perform regular and ad hoc medical reviews of data listings and visualisations; analyse the data to identify risks, patterns and trends, and support documentation of medical reviews. Author medical data queries, review query responses and approve query closure in association with the Medical Director. Assist the Medical Director with patient profile reviews, scientific reviews of study level data, protocol deviation reviews and the creation of Medical Review Summary reports when needed. Partner with Medical Directors for medical data review meetings and safety review meetings, including slide preparation. Manage project scope, objectives and quality of deliverables to ensure project specific milestones and timelines are met; serve as the primary interface between the internal team, customers and vendors in medical data review and eligibility review areas. Collaborate with study team members (Clinical Operations, Data Management, Drug Safety & Pharmacovigilance, Project Management) to identify risks related to data integrity and subject safety; promptly escalat e concerns to the project leads. Attend Trusted Process meetings and may participate in internal and external audits. Acquire a basic understanding of ongoing protocol designs, disease related terminology and pathology. Adhere to data privacy guidelines, ICH, GCP, enterprise policies, SOPs, work instructions, project plans and customer policies. Qualifications MD is required. Minimum two years of direct patient care experience post residency. Must be located in the UK; no sponsorship will be considered. Excellent time management skills to handle multiple tasks and meet deadlines in a highly regulated environment. A self starter comfortable with fluctuating timelines, changing scope and work demands. Ability to troubleshoot situations and determine when to escalation issues to leadership. Understanding of scientific principles to assure effective and high quality medical data analysis. Excellent written and oral communication skills. Strong computer skills: MS Office, spreadsheets, presentations. Preferred knowledge of drug development and proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and capability to work effectively in a cross functional team environment. Additional Information Tasks, duties and responsibilities listed above are not exhaustive. The Company may assign additional duties. Equivalent experience, skills or education will be considered. The Company will determine what constitutes an equivalent qualification. This description complies with all applicable legislation, including the EU Equality Directive and the Americans with Disabilities Act. Equal Opportunity Statement Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, age, religion, marital status, ethnicity, national origin, sex, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any portion of the application process, please contact: .
A global healthcare solutions provider is seeking a Medical Scientist for a 12-month fixed-term contract in the UK. Responsibilities include developing medical plans, analyzing data reviews, and collaborating with various teams. The ideal candidate must hold an MD, have at least two years of direct patient care experience, and be based in the UK. Strong time management and communication skills are essential. This position fosters a dynamic work environment focused on quality and effective medical data analysis.
Apr 21, 2026
Full time
A global healthcare solutions provider is seeking a Medical Scientist for a 12-month fixed-term contract in the UK. Responsibilities include developing medical plans, analyzing data reviews, and collaborating with various teams. The ideal candidate must hold an MD, have at least two years of direct patient care experience, and be based in the UK. Strong time management and communication skills are essential. This position fosters a dynamic work environment focused on quality and effective medical data analysis.