DOCS Global

Country Study Manager / Homebased / UK

6 days left

great perks and package - career scope
09 Feb 2021
11 Mar 2021
Full Time
Contract Type
Experience Level

Country-level Clinical Study Manager / Permanent / Home-based


To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with the client’s Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.

In addition to leading LST(s), the Local Study Manager (LSM) may perform site monitoring as needed to support the flexible capacity model.

The Local Study Manager (LSM) is responsible to ensure that sites are identified, site qualifications performed, set up, initiated,    monitored, closed and documentation archived.

Job Functions/Responsibilities

  • Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
  • Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies
  • Leads and optimises the performance of the Local Study Team(s) at country level ensuring compliance with the client’s Procedural Documents, ICH-GCP and local regulations.
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment and conducting Site Qualification Visits to evaluate suitability and quality risks.
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.
  • Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in the client’s clinical studies financial system by regular checks of the system and financial reports (as agreed with ADSMM/CH).
  • Ensures timely preparation of local Master CSA (including site budget) and amendments as needed.
  • Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant client’s SOPs and local regulations.
  • Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with the client’s SOPs.
  • Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).
  • Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations.
  • Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.
  • Reviews monitoring visit reports (as required and following the client’s SOPs) and pro-actively advices the monitor(s) on study related matters.
  • Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs.
  • Proactively identifies risks and facilitates resolution of complex study problems and issues.
  • Organises regular Local Study Team meetings on an agenda driven basis.
  • Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders.
  • Reports study progress/update to the Global Study Leader/ Global Study Team including SMM Lead.
  • Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.
  • Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.
  • Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.
  • Plans and leads National Investigator meetings, in line with local codes, as required.
  • Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies.
  • Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organised at country level.
  • Ensures accurate payments related to the study are performed according to local regulations and agreements.
  • Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and the client’s Procedural Documents.
  • Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline manner to maintain the eTMF “Inspection Ready”.
  • Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.
  • Plans and leads activities associated with audits and regulatory inspections in liaison with CQM and QA.
  • Provides input to process development and improvement.
  • Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues.
  • Updates Line Managers about the performance of the CRAs/CSAs.
  • Ensures that study activities at country level comply with local policies and code of ethics.
  • Ensures compliance with Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).
  • Collaborates with local Medical Affairs team.
  • Supports SMM in different initiatives (local, regional or global) as agreed with the CH/CD SMM.

What is required

  • Bachelors degree in related discipline, preferably in life science, or equivalent qualification (*).
  • Ideally minimum 3 years of experience as a CRA or Senior CRA or other related fields (Medical Affairs-led or Academic-led studies).
  • Good knowledge of international guidelines ICH-GCP as well as relevant local regulations.
  • Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
  • Excellent project management skills.
  • Excellent team building and interpersonal skills.
  • Excellent organisational skills.
  • Excellent verbal and written communication skills.
  • Excellent ability to prioritize and handle multiple tasks.
  • Good negotiation skills.
  • Good ability to learn and to adapt to work with IT systems.
  • Ability to travel nationally and internationally as required.
  • Good medical knowledge and ability to learn relevant Therapeutic Areas.
  • Good knowledge of the Drug Development Process.
  • Excellent understanding of the Clinical Study Process including monitoring.
  • Very good understanding of the Study Drug Handling Process and the Data Management Process. 
  • Good decision making and delegation skills.
  • Good financial management skills.

What is offered

  • Permanent contract of employment with DOCS seconded to the client;
  • Full-time;
  • Fully home-based or possibility of office-based
  • Competitive salary  depending on level of skills and experience;
  • Company benefits: car allowance paid monthly, 25 days annual leave, pension and healthcare.

    Why Join DOCS?

    If you are an experienced country-level clinical study manager looking for a new career opportunity with a well-established pharmaceutical company, please contact me with your CV today or for more information: or ring +33 964 25 67 65.

    *Applicants who have not had a response within two weeks should assume

    their application has been unsuccessful*

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