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Senior Clinical Data Analyst

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
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Offer summary

Qualifications:

Bachelor's degree in a relevant field, preferably in life sciences or data management., Advanced knowledge of Clinical Data Management Systems and proficiency in at least one system (e.g. InForm, Rave)., Strong problem-solving skills and ability to make decisions in ambiguous situations., Experience in the clinical research industry with a good understanding of ICH-GCP guidelines..

Key responsabilities:

  • Lead and coordinate clinical data validation activities on assigned projects.
  • Interact independently with sponsors to discuss data issues and validation requirements.
  • Provide technical expertise and operational leadership regarding data management processes.
  • Act as a subject matter expert on data management systems and processes, offering support to internal and external stakeholders.

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Parexel XLarge http://www.parexel.com
10001 Employees
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Senior Clinical Data Analyst (SCDA) independently performs/lead and/or coordinate all clinical data validation activities on assigned projects, commensurate with experience and/or project role, with high degree of proficiency and autonomy. Further responsibilities shall include providing technical expertise and/or operational leadership regarding all DM operational activities (data cleaning matrices), processes and Data Management documents regarding data validation. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.
SCDA acts as a subject matter expert on DM Systems/processes, providing technical support and expert advice to internal and external sponsors.
The SCDA may act as a back-up to or fulfill the Data Management Lead role where required.

 

Roles and Responsibilities

  • Proven ability to lead and collaborate with global and cross-functional teams - ability to coordinate & prioritize tasks for the DM operational and programming teams (when) in the Primary CDA role.
  • Ability to independently interact with Sponsor liaison to discuss data issues/project data validation requirements, as needed.
  • Proven negotiation skills and ability to influence in order to achieve mutually beneficial results.
  • Strong problem-solving skills and logical reasoning, including capability to make appropriate decisions in ambiguous situations, ability to conduct root cause analyses.
  • Commitment to first time quality, including a methodical, analytical and accurate approach to work activities (attention to detail).
  • Proven Time management and prioritization skills with a strong sense of urgency - in order to meet objectives.
  • Advanced interpersonal, oral and written communication skills - using concise phrasing tailored for the audience with a diplomatic approach
  • Good presentation skills.
  • Proven learning ability and knowledge sharing approach; swift understanding of technologies and new processes.
  • A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing technical environments.
  • Strong sense of accountability relative to Key Accountabilities in Job Description.
  • Innovative - ability to define strategies to improve efficiency when performing the Data Management tasks.
  • Written and oral fluency in English. Advanced understanding of data management processes and data validation flow (e.g. Data cleaning, DB lock).
  • Good understanding of relevant ICH-GCP Guidelines, local regulatory requirements and PAREXEL SOPs and study specific procedures.
  • Advanced knowledge of Clinical Data Management Systems and proficiency in at least one system (e.g. InForm, Rave, Veeva, DataLabs, ClinBase.)
  • Good understanding of Clinical Study Team roles within Data Management - awareness of DML activities e.g.: budget reviews, resource forecast, etc.
  • Experience in clinical research industry.
  • Advanced knowledge of medical terminology and coding dictionaries (e.g. MedDRA & WHODRUG).
  • Advanced knowledge of Data Management Operational processes and tasks during study start-up, conduct and close-out.
  • Advanced knowledge of Database set-up activities, including but not limited to Database Configuration Specifications and setup of Data Validation.
  • Basic knowledge of SAS (programmed listings).
  • Basic knowledge of Data standards (CDISC).
  • Good understanding of financial principles/drivers for management of DM project financials with regards to forecasting and scope of work.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Problem Solving
  • Social Skills
  • Willingness To Learn
  • Accountability
  • Communication
  • Time Management
  • Detail Oriented
  • Physical Flexibility

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