United States · Remote OK
$111k–$201k/yr
Position Summary: Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are condu…
Skills: Clinical trial management, ICH-GCP, Regulatory compliance, Clinical monitoring, Risk management
Rio de Janeiro, Rio de Janeiro, Brazil · Remote OK
Position Summary: The Change Order Manager will lead change order budget creation activities between project management, functional leads, and the financial analysts in order to develop, explain, and provide variance ana…
Skills: Change order management, Budget creation, Financial analysis, Variance analysis, Project management
Frederick, Maryland, United States · On-site
$18/hr–$26/hr
Position Summary: The Facilities & Cold Storage Technician is responsible for the daily monitoring, and reporting of all environmental storage units. Perform preventive maintenance, repair of refrigeration equipment and …
Skills: Refrigeration maintenance, Preventive maintenance, Low voltage wiring, Equipment monitoring, Temperature sensor calibration
Frederick, Maryland, United States · On-site
$203k–$305k/yr
Position Summary: The Senior Scientific Director, Flow Cytometry will use their scientific expertise to lead development and validation efforts for Flow Cytometry assays to support multiple fast-paced clinical and non-cl…
Skills: Flow cytometry, Assay development, Method validation, Regulatory compliance, GxP
Santiago del Estero, Santiago del Estero, Argentina · Remote OK
We’re hiring a Account Development Manager to help build and lead our expanding clinical offerings across the Americas. This is an exciting, high‑impact opportunity based in LATAM, with a focus on supporting a portfolio …
Skills: Account development, Lead generation, Inside sales, Sales strategy, Relationship management
Houston, Texas, United States · On-site
$76k–$113k/yr
The Senior Histotechnician will be responsible and lead operation and consistent accuracy throughout the processing of tissue sections or staining in the histo-lab; while demonstrating efficient work habits and flexibili…
Skills: Histology, Microtomy, Immunohistochemistry, Tissue processing, Quality control
Rio de Janeiro, Rio de Janeiro, Brazil · Remote OK
We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring our first Senior Regulatory and Start Up Specialist (Senior RSS) in Brazil! As the Senior RSS on our team, yo…
Skills: Regulatory affairs, Site start-up, Clinical trial submission, IRB/EC submissions, Informed consent form review
Rio de Janeiro, Rio de Janeiro, Brazil · Remote OK
Position Summary: The Senior Finance Analyst – Clinical Solutions Portfolio is a strategic, business-partnering role responsible for portfolio-level financial analysis across Clinical Solutions departments. The primary f…
Skills: Financial Analysis, Project Finance, Budgeting, Forecasting, Variance Analysis
Poland · Remote OK
$403k–$604k/yr
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site start-up, Clinical research, People management, GCP/ICH guidelines, Strategic planning
Slovakia · Remote OK
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site Start-up, Clinical Research, Leadership, GCP/ICH Guidelines, Regulatory Compliance
Romania · Remote OK
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site Start-up, Clinical Research, People Management, GCP, ICH Guidelines
Hungary · Remote OK
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site Start-up, Clinical Research, Leadership, Regulatory Compliance, GCP/ICH Guidelines
Spain · Remote OK
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site Start-up, Clinical Research, Leadership, Regulatory Compliance, GCP/ICH Guidelines
United Kingdom · Remote OK
Precision for Medicine is hiring a Director, Site Start up to join our team. We can consider candidates working remotely in the UK, Spain, Poland, Hungary, Serbia, Slovakia or Romania. Position Summary: Provides leadersh…
Skills: Site Start-up, Clinical Research, People Management, GCP/ICH Guidelines, Regulatory Compliance
Poland · Remote OK
$243k–$364k/yr
Precision Medicine Group are hiring a Principal Benefits Partner based remotely in Hungary, Poland or Turkey to join our team. The Principal Benefits Partner will be responsible for the execution and administration of PM…
Skills: Benefits administration, International benefits, Benchmarking, Compensation analysis, Payroll
Hungary · Remote OK
Precision Medicine Group are hiring a Principal Benefits Partner based remotely in Hungary, Poland or Turkey to join our team. The Principal Benefits Partner will be responsible for the execution and administration of PM…
Skills: Benefits administration, International benefits, Compensation analysis, Benchmarking, Payroll
Turkey · Remote OK
Precision Medicine Group are hiring a Principal Benefits Partner based remotely in Hungary, Poland or Turkey to join our team. The Principal Benefits Partner will be responsible for the execution and administration of PM…
Skills: Benefits Administration, International Benefits, Compensation Analysis, Benchmarking, Broker Management
Bangalore, Karnataka, India · On-site
Position Summary: The Central Monitor II will play a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management…
Skills: Clinical monitoring, Risk-based quality management, Statistical data review, Data quality assurance, Clinical trial management
Belgium · Remote OK
Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of b…
Skills: Clinical research, Site management, Monitoring visits, Protocol compliance, Regulatory submissions
Germany · Remote OK
Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. We are n…
Skills: Clinical research, Site management, Protocol compliance, Regulatory submissions, Oncology
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The Clinical Trial Manager is responsible for the planning, conduct, and operational oversight of clinical studies to ensure compliance with protocols and regulatory requirements. They serve as the primary point of contact for clients and lead internal clinical teams to manage site start-up, enrollment, and study maintenance.
Candidates must have a minimum of 7 years of clinical research experience, including significant clinical monitoring experience. A bachelor's degree in a science or health-related field is required, with an advanced degree preferred.
Position Summary:
Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements.
Essential functions of the job include but are not limited to:
Qualifications:
Minimum Required:
Preferred:
Other Required:
Competencies:
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.
A PerkinElmer Company
Project Farma is a patient-focused global leader in advancing technical operations from ideation through commercialization with a proven track record of planning, building, and maintaining manufacturing facilities, capital expansions, and technical operations for complex biologics and novel modalities. We provide end-to-end services for the entire manufacturing lifecycle for pharmaceutical and biotech companies, universities, hospitals, and government agencies. Project Farma has executed 100+ facility builds, retrofits and expansions, managed 400+ large scale capital projects, industrialized 10+ commercial cell, gene, and novel therapies, and managed $6B+ in technical operations capital investments. One of our core values is giving back. Volunteering at hospitals, supporting life science related fundraisers and partnering with nonprofit organizations is an integral part of our culture. In doing so, not only do we raise awareness of many life-threatening diseases, but we also bring our team and our client’s team closer to the actual patients and families that will be impacted by our work. Project Farma is a PerkinElmer company. (https://www.projectfarma.com/)
Offices: 710 Bridgeport Ave, Shelton, Connecticut 06484, US
A PerkinElmer Company
Project Farma is a patient-focused global leader in advancing technical operations from ideation through commercialization with a proven track record of planning, building, and maintaining manufacturing facilities, capital expansions, and technical operations for complex biologics and novel modalities. We provide end-to-end services for the entire manufacturing lifecycle for pharmaceutical and biotech companies, universities, hospitals, and government agencies. Project Farma has executed 100+ facility builds, retrofits and expansions, managed 400+ large scale capital projects, industrialized 10+ commercial cell, gene, and novel therapies, and managed $6B+ in technical operations capital investments. One of our core values is giving back. Volunteering at hospitals, supporting life science related fundraisers and partnering with nonprofit organizations is an integral part of our culture. In doing so, not only do we raise awareness of many life-threatening diseases, but we also bring our team and our client’s team closer to the actual patients and families that will be impacted by our work. Project Farma is a PerkinElmer company. (https://www.projectfarma.com/)
Offices: 710 Bridgeport Ave, Shelton, Connecticut 06484, US
