Full-time
In-House Clinical Research Associate II, Sponsor-Dedicated (Contract)
Competitive
Full-time, ContractScience & PharmaceuticalPosted 20d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
20 days ago
Job description
In-House Clinical Research Associate II, Sponsor-Dedicated (Contract) jobs in United States
Tags
50+ applicants
Original Job Post
Premier Research
70
GOOD MATCH
Experience Level
100
Skill
33
Industry Exp.
81
Health Care
Responsibilities
Partners with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams
Carry out remote monitoring of clinical trials
Serves as the secondary contact for sites supporting CRAs
Responsible for the proper reporting and follow up of SAEs and ensures all reportable events are identified, clearly documented and reported per protocol as well as applicable requirements and regulations
Ensures any identified non-compliance issues are addressed, clearly communicated, documented and escalated as required through monitoring visits, analyzing study metrics, and general study data overview
Assists with audit/inspection readiness, study start-up activities, data listing reviews, monitoring visit support and issue resolution
Preferred
Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
preferably in a clinical, biological, scientific, or health-related field
Preferred Location: East Coast / Central
Benefits
Remote work
Flexibility and balance your life requires
Glassdoor
3.4
Global clinical research and consulting services for life sciences.
Morrisville, North Carolina, USA
https://premier-research.com
Distribution of Different Job Fields Receiving Sponsorship
80
Represents job field similar to this job
Engineering and Development
Legal and Compliance
Management and Executive
Accounting and Finance
Customer Service and Support
Trends of Total Sponsorships
*2026
(5)
2025
(9)
2024
(10)
2023
2022
(19)
2021
(17)
2020
(6)
Late Stage
Qualifications
Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience
3 to 5 years of practical experience in clinical trials. Alternately, a proven experience in all primary job functions
Demonstrates excellent English verbal and written communication skills
Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverable, and task ownership
Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
Preferably in a clinical, biological, scientific, or health-related field
Preferred Location: East Coast / Central
Required skills
Represents the skills you have, click on the tags, Neurology, Psychiatry, Schedule I Controlled Substances
Preferred skills
Preferred Location: East Coast / Central
Experience
3-5 years
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