Top 9 Cra Jobs in Smithfield Nc

Clinical Research Associate II/III - US
Optimapharm d.o.o. —Raleigh, NC
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Dental insurance
- Paid time off
Drug Safety Scientist
Grifols —Clayton, NC
- Full-time
- Computer literacy
- Bachelor of Science
- Mid-level
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Raleigh, NC
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
Sr Clinical Research Associate
Veranex, Inc. —Raleigh, NC
- $98,400 - $140,690 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Senior Clinical Project Manager
Azurity Pharmaceuticals - US —Raleigh, NC
- Full-time
- Hybrid work
- 5 years
- Office
- Ability to climb stairs
- Fuel card
- Health insurance
3h

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Senior Clinical Research Associate - US
Optimapharm d.o.o. —Raleigh, NC
A current, valid driver’s license. At least 3-5 years of independent clinical trial monitoring experience in oncology.
$100,000 - $130,000 a year
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Raleigh, NC
A current, valid driver’s license. At least 2 years of independent clinical trial monitoring experience. Being part of a clinical research team that transforms…
$75,000 - $100,000 a year

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Clinical Research Associate II/III - US

Optimapharm d.o.o.
Raleigh, NC

Apply Now

Job Details

Full-time
$75,000 - $100,000 a year

Benefits

Dental insurance
Paid time off
Pension plan
Vision insurance

Qualifications

ICH guidelines
Bachelor's degree
Clinical quality assurance standards
Contract negotiation
Cross-functional collaboration
Technical Proficiency

Full Job Description

Location: Remote

Who we are?

Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I–IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence.

With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. At Optimapharm, you’ll contribute to meaningful clinical research while growing your career in a dynamic, people‑focused, global environment.

As we expand our US Clinical Operations team, we're searching for a CRA II/III who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives.

Joining Optimapharm means more than taking on your next role - it's an opportunity to build a long-term career with a global CRO that values growth, development, and excellence. Our structured career pathway provides clear progression and recognition of your expertise: CRA I CRA II CRA III Senior CRA.

Here, your dedication is rewarded with meaningful growth opportunities, exposure to diverse studies, and the support needed to reach your full potential.

What do we offer?

Working in a successful company that’s growing and developing every day
Being part of a clinical research team that transforms science into hope for patients
International projects and professional growth
Company that supports life balance
Company with healthy culture
Working with a highly experienced team of clinical research professionals
Competitive salary
Competitive PTO entitlement
Health insurance, including vision and dental plans, to meet your and your family's needs
Comprehensive pension plan to maximize savings and prepare confidently for the future
Employee engagement programs
Well-being initiatives
Training and development program
Fast-paced career path progression

Who are we looking for?

Qualifications and Experience

University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
At least 2 years of independent clinical trial monitoring experience
High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
Computer proficiency is mandatory
Ability to read, analyze, and interpret common scientific and technical journals
Excellent verbal and written communication skills
Very good interpersonal and negotiation skills
Ability to work independently, pro-active
Affinity to work effectively and efficiently in a matrix environment
A current, valid driver’s license

Your responsibilities

Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits
Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable
Identifying and escalating potential risks and identifying retraining opportunities for site personnel
Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution
Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor
Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable
Administration of site payments in accordance with relevant project instructions

By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.

If you would be interested in joining the Optimapharm team, please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.

Compensation is competitive and final offers will reflect each candidate’s experience, skills, and qualifications.

Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.

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cra jobs in smithfield nc

Clinical Research Associate II/III - US

Drug Safety Scientist

Senior Clinical Research Associate - US

Sr Clinical Research Associate

Senior Clinical Project Manager

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