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Skills: Registered Nurse, Clinical Research, Patient Care, Good Clinical Practice, Documentation
San Francisco, California, United States · Remote OK
$132k–$175k/yr
Senior$579M raised
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TJT
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Part-time
professional certificate
Posted 9d ago
~40 hrs/week
Responsibilities
The Registered Nurse will provide quality clinical research services to patients at locations outside of investigator sites, such as homes or offices. They are responsible for completing study-specific requirements, maintaining accurate source documentation, and communicating patient safety concerns to the project team.
Requirements
Candidates must hold an active, unencumbered RN license in the US with at least 2 years of post-graduate experience. Proficiency in clinical research practices, Basic Life Support certification, and the ability to travel with necessary medical equipment are required.
Full job description
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Key Responsibilities:
Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school). Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems. Completes source documentation during DCVs following Good Documentation Practice and submits source to project team in a timely manner. Communicates issues and patient safety concerns to GCPM, GCPC, and investigator site as appropriate. Physically able to perform assigned nursing tasks and lift equipment up to 25lbs in weight. Access to a reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).
Qualifications: Education & Experience
Active, unencumbered RN licensure or certification in US
Multistate practice/licensure preferred where applicable Minimum 2+ years post-graduate experience Clinical research experience preferred Basic Life Support (BLS) Certification
Preferred Skills
Ability to communicate in English (both verbal and written). Flexible and able to make quick accommodations to schedule changes as well as process changes and to travel with limited notice. Ability to work afterhours or weekends preferred. Computer skills/experience. Working knowledge of MS Office suite and Google applications. Willingness to gain expertise in the use of propriety eSource software. Organized and able to multitask; prioritizes based on protocol and visit parameters. Consistent preparedness for specific visits requirements as well as equipment and additional supplies for potential trouble shooting at the visit.
Additional Information: All candidates must be legally eligible to work in the US
#LI-mk1
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.
End-to-end bespoke solutions that de-risk & accelerate our partners' and sponsors' drug and device development programs
Industry
Business Consulting and Services
Company size
1,001-5,000 employees
Founded
2001
Headquarters
Raleigh, North Carolina
LinkedIn followers
202,745
Total funding
$9M
At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success.
Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risks and accelerates high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
Offices: 107 W Hargett St, Raleigh, North Carolina 27601, US · Olliver, Richmond, North Yorkshire DL10 5HX, GB · Schipholweg 59, P.O. Box 255, Leiden, AG 2316 ZL, NL · Siemensdamm 62, Berlin, Germany 13627, DE · Solnavägen 3H, 113 63 Stockholm, Sweden, Stockholm, Stockholm County SE -112, SE
How many Consulting jobs are open in Raleigh, NC right now?
There are currently 1,011 open consulting positions in Raleigh, NC listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Consulting roles in Raleigh, NC?
Companies currently hiring include ProPharma, AECOM, JMT, ECS Group of Companies, Cherry Bekaert, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Consulting jobs in Raleigh, NC?
Yes — 501 of the 1011 open consulting positions offer remote or hybrid work (142 remote, 359 hybrid).
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