ParexelPA

Senior Clinical Data Analyst

Parexel is a leading global CRO that specializes in clinical research and biopharmaceutical services to bring lifesaving treatments to patients faster.

Parexel

Employee count: 5000+

India only

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.

About the job

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Posted on

Job type

Full Time

Experience level

Senior

Location requirements

Hiring timezones

India +/- 0 hours

About Parexel

Learn more about Parexel and their company culture.

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At Parexel, we speed your life-changing medicines to patients through innovative and efficient clinical research. We are proudly among the world's largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. With a dedicated team of over 21,000 global professionals, we partner with biopharmaceutical leaders to design and deliver clinical trials that prioritize patient needs and experiences.

In a fast-evolving healthcare landscape, our commitment to inclusivity and diversity in clinical trial participation sets us apart. We focus on ensuring that clinical research is accessible and representative, fostering stronger relationships with communities to enhance healthcare equity. Our approach brings an empathetic focus to clinical trials, ensuring every patient’s voice is heard and valued. By adhering to our core values—Patients First, Quality, Respect, Empowerment, and Accountability—we strive for excellence in every aspect of our work, making a difference in patients' lives globally.

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