TMF Specialist

Bachelor's in life sciences or public health; 1-2 years in clinical trials; TMF Reference Model, TMF Indexes, electronic TMF systems; interpret TMF index; strong communication; commitment to quality.

CMC Regulatory Strategist

Regulatory Strategist

PhD/PharmD or equivalent; 12+ years in development programs with inter-related clinical, nonclinical, CMC and regulatory experience; FDA experience required; strong regulatory intuition and leadership; excellent communication and project management; proficient with MS Project, Visio, Excel, PowerPoint, Word.

Clinical Research Associate II / Sr. CRA (Neurology/Parkinsons - Central)

Clinical Research Associate

BA/BS in life sciences with 4-5 years on-site monitoring in CRO/pharma/biotech; MS Office proficiency; strong communication; detail-oriented; adaptable.

Clinical Research Associate II / Sr. CRA (Major Depressive Disorder West Coast)

Clinical Research Associate II

BA/BS in life sciences with 4-5 years on-site monitoring in CRO/pharma; MS Office and EDC proficiency; strong communication; quality focus; teamwork; critical thinking; adaptability.

Quality Risk Manager

At least 6 years of industry experience; expert in GCP/ICH E6(R2); experience in RBQM strategies; strong computer skills; advanced MS Excel; data visualization; analytical and communication skills; travel ~15%.

Study Start Up Lead

4+ years industry experience, 2+ years SSU leadership; regulatory knowledge (ICH-GCP/EU directives); strong communication; organizational; travel 10%.

At least 4 years of industry experience, including 2+ years in study start-up leadership; strong leadership, regulatory knowledge (ICH-GCP/EU directives), risk management, and communication abilities; proficient with MS Office; willing to travel ~10%.

At least 4 years of industry experience with 2+ years in study start-up leadership; strong regulatory knowledge; capable of leading teams and coordinating cross-functional efforts.

At least 4 years in the industry, with 2+ years leading study start-up; strong leadership, regulatory knowledge (ICH-GCP/EU), submissions, risk management, communication, organization, and travel readiness.

At least 4 years industry experience, including 2+ years in study start-up leadership; regulatory knowledge (ICH-GCP/EU directives); strong leadership, communication, organizational and strategic thinking skills; travel ~10%; remote work.

At least 4 years in the industry, including 2+ years leading study start-up; regulatory and submission knowledge; strong communication and organizational skills; willingness to travel ~10%.

Senior Clinical Research Associate, Poland

Senior Clinical Research Associate

Bachelor’s in life sciences or nursing; RN or equivalent with 2+ years of clinical monitoring; 2 years CRO/Pharma/biotech monitoring experience; English + local language; ICH-GCP knowledge; ability to travel up to 80%; team mentoring and study support.

In-House Clinical Research Associate

Bachelors in life sciences, nursing, or pharmacy with 1+ year experience handling essential regulatory documents in CRO/pharma/biotech; knowledge of ICH/GCP; eagerness to become a traveling CRA; strong communication in English and local language; detail-oriented with high professional integrity.

Bachelor's degree in life science, nursing, or pharmacy with at least 1 year of direct work experience handling essential documents in CRO/pharma/biotech; knowledge of clinical research processes, regulatory and ethics submissions; aim to grow into traveling CRA; strong English and local language communication; high attention to quality and integrity; adaptable and collaborative mindset.

Bachelor’s in life science, nursing, or pharmacy with 1+ year CRO/pharma/biotech document management experience; strong ICH/GCP knowledge; English fluency; desire to travel as a CRA.

Bachelor’s in life sciences/nursing/pharmacy; 1+ year CRO/pharma documentation experience; knowledge of clinical research, regulatory submissions, ICH GCP; aim to become traveling CRA; fluent in English and local language; detail-oriented; adaptable; collaborative.

Bachelor's in life sciences/nursing/pharmacy with 1+ year experience managing essential documents in CRO/pharma/biotech; knowledge of clinical research processes, regulatory/ethics submissions, ICH/GCP; desire to grow into traveling CRA; strong communication; commitment to quality; high character; agile/adaptive.

Bachelor's degree in life sciences, nursing, or pharmacy plus 1 year of direct documents management experience in CRO/pharma/biotech; knowledge of ICH-GCP and regulations; English proficiency; desire to travel.

Freelance Regional Clinical Trial Manager

Regional Clinical Trial Manager

Degree in life sciences or nursing with at least 5 years of clinical trial management experience; multi-site/CRO experience; strong English communication; travel readiness; valid driver’s license.

Degree in life sciences or related field with 5+ years in clinical trial management, regional/multi-site experience; English proficient; travel and driver’s license; detail-oriented and ethical.

Senior Clinical Project Manager

BS in life sciences with 5+ years managing large clinical research projects; GCP/ICH knowledge; on-site monitoring or CRA team mgmt; strong communication; quality focus; agile/adaptable.

Financial Systems Administrator (NetSuite, Concur, FloQast)

Financial Systems Administrator

Bachelor's degree in a related field; 3–5+ years NetSuite admin experience; strong integration, reporting, and data management skills; Oracle NetSuite certification preferred; experience with CRO or project-based orgs; excellent analytical and communication abilities.

Clinical Research Associate II / Sr. CRA (Central or West Coast)

BA/BS in life sciences with 4-5 years of on-site monitoring in CRO/pharma/biotech; proficient in MS Office and EDC; strong communication; detail-oriented; team-focused; able to adapt and think critically.

Medical Director / Senior Medical Director (Pain Experience)

Medical Director

Medical degree with active medical license; 5+ years in clinical medicine post-residency and 5+ years in clinical development, pain-management focus; knowledge of trial design, biostatistics, and regulatory guidelines; ability to manage priorities and communicate effectively.

Clinical Team Lead

8+ years in clinical research (CRO/pharma/biotech); 1-2 years leading clinical operations; 2+ years on-site monitoring; BA/BS in life sciences; strong communication; quality-focused; adaptable; travel up to 25%.

Title	Location	Date
TMF Specialist Full Time · 1+ YOE Warsaw or Poland · Remote	Warsaw or Poland Remote	Apr 24, 2026
CMC Regulatory Strategist Full Time · $190K-$210K · 12+ YOE United States · Remote	United States Remote	Apr 21, 2026
Clinical Research Associate II / Sr. CRA (Neurology/Parkinsons - Central) Full Time · $90K-$140K · 4+ YOE United States · Remote	United States Remote	Apr 17, 2026
Clinical Research Associate II / Sr. CRA (Major Depressive Disorder West Coast) Full Time · $90K-$140K · 4+ YOE United States · Remote	United States Remote	Apr 17, 2026
Quality Risk Manager Full Time · $95K-$108K · 6+ YOE United States · Remote	United States Remote	Apr 14, 2026
Study Start Up Lead Full Time · 4+ YOE Bulgaria · Remote	Bulgaria Remote	Apr 8, 2026
Study Start Up Lead Full Time · 4+ YOE Italy or Spain or Poland or Latvia or Lithuania or Bulgaria · Remote	Italy or Spain or Poland or Latvia or Lithuania or Bulgaria Remote	Apr 8, 2026
Study Start Up Lead Full Time · 4+ YOE Spain · Remote	Spain Remote	Apr 8, 2026
Study Start Up Lead Full Time · 4+ YOE Lithuania or Italy or Spain or Poland or Latvia or Bulgaria · Remote	Lithuania or Italy or Spain or Poland or Latvia or Bulgaria Remote	Apr 8, 2026
Study Start Up Lead Full Time · 4+ YOE Latvia · Remote	Latvia Remote	Apr 8, 2026
Study Start Up Lead Full Time · 4+ YOE Poland · Remote	Poland Remote	Apr 8, 2026
Senior Clinical Research Associate, Poland Full Time · 2+ YOE Poland · Remote	Poland Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time · 1+ YOE Estonia · Remote	Estonia Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time · 1+ YOE Lithuania · Remote	Lithuania Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time, Part Time, Contract, Internship, Temporary, Seasonal, Volunteer · 1+ YOE Latvia · Remote	Latvia Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time · 1+ YOE Spain · Remote	Spain Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time · 1+ YOE United Kingdom · Remote	United Kingdom Remote	Apr 2, 2026
In-House Clinical Research Associate Full Time · 1+ YOE Poland · Remote	Poland Remote	Apr 2, 2026
Freelance Regional Clinical Trial Manager Contract · 5+ YOE Latvia · Remote	Latvia Remote	Apr 2, 2026
Freelance Regional Clinical Trial Manager Contract · 5+ YOE Poland · Remote	Poland Remote	Apr 2, 2026
Senior Clinical Project Manager Full Time · $110K-$150K · 5+ YOE United States · Remote	United States Remote	Apr 2, 2026
Financial Systems Administrator (NetSuite, Concur, FloQast) Full Time · $90K-$120K · 3+ YOE United States · Remote	United States Remote	Mar 27, 2026
Clinical Research Associate II / Sr. CRA (Central or West Coast) Full Time · $90K-$140K · 4+ YOE United States · Remote	United States Remote	Mar 27, 2026
Medical Director / Senior Medical Director (Pain Experience) Full Time · 5+ YOE United States · Remote	United States Remote	Mar 20, 2026
Clinical Team Lead Full Time · $130K-$150K · 8+ YOE United States · Remote	United States Remote	Mar 19, 2026

Activities	clinical trial managementbiostatistical analysisregulatory submission planningclinical data managementmedical monitoring
Headquarters	US
Industries	PharmaceuticalsBiotechnology
Name	Rho
Employees	1,000
Type	Private
Subsidiaries	Dokumeds
Tagline	Provides clinical research services to advance drug development programs.
Founded	1,984
Website	rhoworld.com
Latest Funding Round	Grant
Latest Funding Year	2,021
Latest Funding Amount	369,000
Latest Investors	Public Health EmergencyHHS

Rho

About Rho