Worldwide Clinical Trials

Clinical Research Associate II or SCRA - Poland

5 days left

Location
Warsaw (PL)
Salary
Competitive
Posted
25 Jul 2019
Closes
24 Aug 2019
Ref
VN2313
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Worldwide Clinical Trials are looking for an experienced Clinical Research Associate II or Senior CRA on a Permanent basis with IMID or CNS Therapeutic Area Experience.

Ideally office based from our Warsaw office but home-based will be considered if located in major city such as Lodz, Gdansk or Krakow.

SUMMARY:                       


Responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
 
RESPONSIBILITIES:
Tasks may include but are not limited to:

  • Perform feasibility studies for potential sites as requested
  • Conduct pre-study, study initiation and interim monitoring visits in adherence to the protocol requirements
  • Function in the role of Lead CRA for global studies, coordinating CRAs
  • Develop Clinical Monitoring Plan as requested
  • Conduct site visit trip report review and provide feedback and edits
  • Provide mentoring and guidance to less experienced CRAs and site staff when needed
  • Design study specific tools and templates as requested
  • Actively participate in study team and investigator meetings
  • Actively participate in bid defenses
  • Create and conduct training to study team members or colleagues as requested and appropriate
  • Work with Project Management to evaluate deliverables and study milestones
  • Compile and ensure completeness of regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB / IEC study approval, informed consent, etc.)
  • Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study site
  • Document site visit findings via written reports
  • Provide input into the design of protocols and CRFs as requested
  • Assess, monitor, and train study site staff on protocol adherence as required
  • Review study subject safety information and informed consent
  • Conduct source document verification for compliance, patient safety, and veracity of data
  • Review CRFs using paper or electronic data capture systems and assist sites with data query resolution
  • Assist the site in maintenance of the Investigator Site File
  • Maintain regular communication with sites
  • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
  • Ensure site compliance with IP receipt, accountability and return or destruction
  • Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate
  • Complete final site close out visit and report

 
Perform other duties as assigned.  The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
 
 
OTHER SKILLS AND ABILITIES:

  • Excellent oral and written communication skills
  • Excellent planning and organizational skills with effective time management
  • Excellent interpersonal skills
  • Demonstrate initiative and problem solving skills
  • Ability to lead and motivate assigned team (if applicable)
  • Ability to provide experience and input into process initiatives and development relating to monitoring and site management activities
  • Extensive understanding of clinical research principles and process
  • Through understanding of FDA and/ or EU Directives and regulations, ICH Guidelines and local regulatory requirements
  • Through understanding of two to three therapeutic areas sufficient to function as a Lead CRA as appropriate
  • Thorough understanding of standard operating procedures
  • Proficiency in Microsoft Office
  • Proficiency with IxRS, EDC systems

 
REQUIREMENTS:

  • Medical Doctor (MD) degree or Pharmacist (MSPH, PharmD, PhD, or equivalent Pharmacy degree, etc. ) and with a minimum experience of three years as a Clinical Research Associate OR
  • A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy or other related science and a minimum experience of five years as a Clinical Research Associate, OR
  • Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree preferred) and a minimum seven years as a Clinical Research Associate
  • Willingness to travel required
  • Valid current passport required
  • Driving license required
  • Fluent in the local languages of the countries under responsibilities and proficient in both spoken and written English
  • CNS and/or IMID Therapeutic Area Experience

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