Syneos Health

CRA II or SCRA - Denmark - home based

Salary
Competitive
Posted
14 Jan 2019
Closes
14 Feb 2019
Ref
18010192

CRA II / SCRA II

Home based Denmark

Full time permanent position

General Medicine

 

The Senior Clinical Research Associate II (SCRA II) will perform monitoring and site management activities for Phase I-IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites (either on site or remotely) and to ensure clinical projects are conducted, recorded, and reported in accordance with the protocol, Company and Sponsor standard operating procedures (SOPs), ICH-GCP, and all applicable local and federal regulatory requirements.  Performs all tasks routinely and independently.  Mentors and/or trains, as well as may assume line management responsibilities for less experienced employees. May assume clinical functional leadership tasks as assigned, acting as Lead CRA for a project.

 

JOB RESPONSIBILITIES

 

·        Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance.  Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans.  Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.

 

·        Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.

 

·        Per the Clinical Monitoring/Site Management Plan (CMP/SMP):

 

o   Assesses site processes

o   Conducts Source Document Review of appropriate site source documents and medical records

o   Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records

o   Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines

o   Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture

o   Verifies site compliance with electronic data capture requirements.

 

·        May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.

 

·        Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. 

 

·        Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.  Supports subject/patient recruitment, retention and awareness strategies.  Enters data into tracking systems as required to track all observations, ongoing status and action items to resolution.

 

·        Understands project scope, budgets, and timelines for own and others’ activities in the clinical team; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.  Must be able to quickly adapt to changing priorities to achieve goals / targets. 

 

·        May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.  Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.

 

·        Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.  Participates in and may lead global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.      

 

·        Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.  

 

 

·        May provide direct supervision, training and/or mentorship to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned.

 

·        May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager. This could include participation in business development proposals and/or defense meetings.

 

·        For Real World Late Phase (RWLP), the Sr. CRA II will use the business card title of Sr.Site Management Associate II.  Additional responsibilities include:

 

o   Site support throughout the study lifecycle from site identification through close-out

o   Knowledge of local requirements for real world late phase study designs

o   Chart abstraction activities and data collection

o   As required, collaborate and build relationship with Sponsor and other affiliates, medical science liaisons and local country staff

o   The SMA II may be requested to train junior staff

o   Identify and communicate out of scope activities to Lead CRA/Project Manager

o   Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations.

o   Identify operational efficiencies and process improvements

o   Develop study and country level informed consent forms

o   Collaborate with RWLP Regulatory team to ensure updated regulatory information is applied and shared

o   Participate in bid defense meetings

o   Provide input into Requests for Proposals (RFPs), scope and budgeting.  Develop site management strategy. 

o   Participate in Case Report Form design and edit check development.

 

 

QUALIFICATION REQUIREMENTS

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
  • Must demonstrate good computer skills and be able to embrace new technologies
  • Excellent communication, presentation and interpersonal skills. Moderate level of critical thinking skills expected.
  • Ability to manage required travel of up to 50% on a regular basis