8 days ago

Clinical Scientist

Parexel

Hybrid
Full Time
$120,000
Hybrid

Job Overview

Job TitleClinical Scientist
Job TypeFull Time
CategoryCommerce
Experience5 Years
DegreeMaster
Offered Salary$120,000
LocationHybrid

Who's the hiring manager?

Sign up to PitchMeAI to discover the hiring manager's details for this job. We will also write them an intro email for you.

Uncover Hiring Manager

Job Description

Job Purpose

The Clinical Scientist assists the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.

Key Accountabilities

Responsibilities for the Clinical Scientist role may include, but are not limited to, the following:

  • Clinical Trial Operational Delivery: May support a single study or multiple studies, and could lead a study with limited scope (e.g., Survival Follow-up). This role involves liaising with cross-functional lines as appropriate and interacting with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives.
  • Compliance with Parexel Standards: Ensures compliance with the required training curriculum, accurately completes timesheets, submits expense reports as required, and maintains an updated CV. The Clinical Scientist will maintain a working knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements.

Skills

  • Demonstrated oral and written communication skills
  • Proficiency in MS Office Suite, including Word, Excel, and PowerPoint
  • Advanced Excel skills required (pivot tables, v-lookups)
  • Proficient in written and spoken English
  • Willingness to travel as required for key company meetings

Knowledge And Experience

  • Pharmaceutical experience beneficial but not required
  • Oncology experience is required
  • 2 years medical monitoring experience preferred
  • Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management

Education

  • Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
  • If no degree in Life Sciences, a Bachelor's degree with significant experience in clinical development (>5 years) is required.

Key skills/competency

  • Clinical Research
  • Medical Monitoring
  • Oncology
  • ICH-GCP
  • Protocol Deviation Management
  • Adjudication Support
  • Data Reconciliation
  • Clinical Study Conduct
  • Cross-functional Collaboration
  • Microsoft Excel (Advanced)

Tags:

Clinical Scientist
Clinical Research
Medical Monitoring
Oncology
ICH-GCP
Protocol Deviation Management
Adjudication Support
Data Reconciliation
Clinical Study Conduct
Cross-functional Collaboration
MS Office
Excel
Word
PowerPoint
Clinical Trial Management
Regulatory Compliance
Life Sciences
Clinical Development
Stakeholder Management
Clinical Data

Share Job:

How to Get Hired at Parexel

  • Research Parexel's culture: Study their mission, values, recent news, and employee testimonials on LinkedIn and Glassdoor. Understand their global CRO leadership.
  • Tailor your resume for Clinical Scientist roles: Highlight relevant experience in clinical study conduct, medical monitoring, and oncology. Use keywords from the job description.
  • Prepare for technical interviews: Be ready to discuss ICH-GCP, clinical trial phases, and specific experiences with adjudication or protocol deviation management.
  • Showcase your oncology expertise: Emphasize any oncology-specific research or clinical experience during your application and interviews.
  • Demonstrate strong communication skills: Practice articulating your experience clearly, as effective liaison and meeting material preparation are key to success at Parexel.

Frequently Asked Questions

Find answers to common questions about this job opportunity

Explore similar opportunities that match your background