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Clinical Data Associate

2 months ago

Elk Grove Village, United States Jobot Full time
San Diego based Biotech looking for Clinical Data Associate - Contract Opportunity

This Jobot Consulting Job is hosted by: Victoria Casal
Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.
Salary: $40 - $50 per hour

A bit about us:

Biotechnology company based in San Diego, that specializes in discovering and developing RNA-targeted therapeutics

Why join us?
  • Competitive hourly rate
  • Benefits (medical, dental and disability)
  • Work remote if not in SoCal or hybrid if local to San Diego

This is a temp to hire position with 40 hours a week

Job Details

Responsibilities:
As a Consulting Clinical Data Associate, you will:

1. Assist in the design and implementation of EDC systems and other data management tools.
2. Ensure compliance with ICH guidelines, Good Clinical Practice, and regulatory requirements.
3. Utilize Medidata Rave and other CDMS to monitor and manage data.
4. Develop and maintain DMP and SAPS to ensure the integrity and quality of clinical data.
5. Perform data entry, validation, and quality checks on clinical data.
6. Assist in the creation and maintenance of eCRF.
7. Work closely with cross-functional teams to meet project timelines and goals.
8. Contribute to the continuous improvement of data management processes and systems.
9. Provide training and support to study teams on data management tools and processes.

Qualifications:
To be considered for the Consulting Clinical Data Associate role, you must have:

1. A Bachelor’s degree in Life Sciences, Biostatistics, or a related field.
2. Minimum of 2 years of experience in clinical data management in the pharmaceutical or biotech industry.
3. Proficiency in EDC, ICH guidelines, Medidata Rave, CDMS, DMP, SAPS, and NIH standards.
4. Experience in data entry, quality checks, and eCRF.
5. Strong analytical skills with the ability to identify and resolve data-related issues.
6. Excellent communication and interpersonal skills with the ability to work effectively in a team-based environment.
7. High level of attention to detail and accuracy.
8. Ability to manage multiple projects and meet deadlines.
9. Familiarity with regulatory requirements related to data management in clinical trials.

Interested in hearing more? Easy Apply now by clicking the "Apply Now" button.