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Clinical Research Nurse Practitioner - Onsite

0-2 years
Not Disclosed
10 June 2, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Clinical Research Nurse Practitioner - Onsite

Job ID:

R-01275808

Location:

Birmingham, Alabama, United States (Fully Onsite)

Job Type:

Full-time

Work Schedule:

Standard (Monday–Friday)

Work Environment:

Office setting with occasional travel to clinical sites, domestic and international travel required. On-call coverage occasionally required.


Company Overview:

Thermo Fisher Scientific is a global leader in science, committed to enabling customers to make the world healthier, cleaner, and safer through innovative therapies and research solutions. The Clinical Research team powers the PPD® clinical research portfolio, conducting trials in 100+ countries and innovating clinical research frameworks.


Division Specific Information:

AES (a division of PPD Clinical Research Services) focuses on optimizing patient enrollment and site performance with 150+ clinical research sites worldwide. AES partners with One Tree Planted to support environmental sustainability.


Role Summary:

Serve as Sub-Investigator supporting the Principal Investigator with scientific and medical oversight in clinical trials. Evaluate compounds for subject safety, review medical data, and collaborate with clients and operational teams.


Key Responsibilities:

  • Review protocols for scientific, logistical, and safety feasibility.

  • Conduct assigned roles per protocol and delegation documents.

  • Ensure compliance with informed consent and IRB approvals.

  • Review and sign off on regulatory documents as Sub-Investigator.

  • Research compounds for subject safety.

  • Assess new clinical technologies (e.g., e-consent, automated scheduling).

  • Attend internal meetings for training, protocol discussion, and client updates.

  • Train staff on licensure, malpractice, and new procedures.

  • Support client consultations on study scheduling and assignments.

  • Travel with operational/business development staff to conferences and scientific meetings.

  • Prepare and review scientific posters, papers, and publications.


Candidate Requirements:

Education & Certification:

  • Master’s Degree in Nursing

  • APRN Prescriptive Authority

  • AANP Board Certified

Experience:

  • Clinical research or sub-Investigator experience preferred

  • Knowledge of regulatory considerations, drug safety assessment, and drug development process

  • Familiarity with clinical study guidelines and marketing authorization processes

Skills & Abilities:

  • Strong analytical, decision-making, negotiation, and influencing skills

  • Excellent communication and English fluency

  • Detail-oriented and organized leadership style

  • Proficient with basic computer applications

  • Ability to work independently and as part of a team

  • Flexibility to travel domestically and internationally


Physical Requirements:

  • Primarily office-based with exposure to office equipment

  • Frequent sitting (6-8 hours/day) with repetitive hand movements

  • Occasional physical activities such as bending, stooping, and lifting up to 15-20 lbs

  • Ability to handle variable tasks and work under stress


Benefits:

Competitive salary, annual incentive plan bonus, healthcare, and a comprehensive range of employee benefits. Culture focused on integrity, intensity, involvement, and innovation.