Romania · Remote OK
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precisio…
Skills: Clinical Trial Management, Oncology, GCP/ICH Guidelines, Site Selection, Enrolment Management
Serbia · Remote OK
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precisio…
Skills: Clinical Trial Management, Oncology, GCP/ICH Guidelines, Site Selection, Enrolment Management
Poland · Remote OK
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precisio…
Skills: Clinical Trial Management, Oncology, GCP/ICH Guidelines, Site Selection, Enrolment Management
Hungary · Remote OK
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precisio…
Skills: Clinical Trial Management, Oncology, GCP/ICH Guidelines, Site Selection, Enrolment Management
India · Remote OK
Position Summary: The Analyst, Business and Competitive Intelligence is responsible for the identification, information gathering, planning and coordinating of sales-based communication activities for a selection of desi…
Skills: Competitive Intelligence, Business Development, Lead Qualification, Outbound Prospecting, Market Research
Paris, Ile-de-France, France · Remote OK
Precision for Medicine is looking for a Senior Site Contracts Manager to join our FSP group in Europe. We are looking for someone with extensive site contracts and budgets experience across European region. This position…
Skills: Site contract management, Budget negotiation, Clinical trial agreements, Legal agreement drafting, Clinical operations
Canada · Remote OK
$149k–$246k/yr
Position Summary: Provides statistical leadership and support for all phases of clinical development. Specific responsibilities include consulting with clients regarding clinical trial study design and regulatory strateg…
Skills: Statistical leadership, Clinical trial study design, Regulatory strategy, Statistical analysis plans, Sample size calculations
United States · Remote OK
$147k–$243k/yr
Position Summary: Provides statistical leadership and support for all phases of clinical development. Specific responsibilities include consulting with clients regarding clinical trial study design and regulatory strateg…
Skills: Statistical leadership, Clinical trial study design, Regulatory strategy, Statistical analysis plans, Sample size calculations
Frederick, Maryland, United States · On-site
$25/hr–$38/hr
Position Summary: The Processing Team Lead provides technical leadership and daily operational coordination within the sample processing laboratory while performing complex biological sample processing activities. This r…
Skills: Sample processing, Laboratory operations, Cryopreservation, Aseptic technique, Data management
Germany · Remote OK
Position Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing au…
Skills: Regulatory strategy, Companion diagnostics, IVD development, FDA regulations, EU IVDR
France · 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 Monitoring, Oncology, Regulatory Submissions, ICH-GCP
United States · Remote OK
$111k–$166k/yr
Position Summary: Responsibilities will include but may not be limited to; project specific teleconferences/meetings(i.e. Kick off meetings, internal study specific meetings, client governance meetings) Safety budget rev…
Skills: Pharmacovigilance, Clinical safety, SAE case management, Regulatory reporting, MedDRA
United Kingdom · Remote OK
Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical docume…
Skills: Clinical Document Planning, Medical Writing, QC Review, Regulatory Compliance, Clinical Study Protocols
Romania · Remote Solely
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and m…
Skills: Project Timeline Management, Meeting Coordination, Clinical Trial Management System (CTMS), Trial Master File (TMF), Training Record Management
Slovakia · Remote OK
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and m…
Skills: Project Timeline Management, Meeting Coordination, Clinical Trial Management System (CTMS), Trial Master File (TMF), Training Record Management
Poland · Remote Solely
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and m…
Skills: Project Timeline Management, Meeting Coordination, CTMS, Training Record Management, SharePoint
Hungary · Remote OK
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and m…
Skills: Project Timeline Management, Meeting Coordination, Clinical Trial Management System (CTMS), Trial Master File (TMF) Management, Training Record Maintenance
Serbia · Remote OK
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and m…
Skills: Project Timeline Management, Meeting Coordination, Clinical Trial Management System (CTMS), Trial Master File (TMF), Training Record Management
Canada · Remote OK
$93k–$139k/yr
Position Overview We are seeking a highly organized and detail-oriented Marketing and Events Manager to lead the planning, execution, and optimization of our event marketing initiatives globally. This role is ideal for a…
Skills: B2B Event Management, Marketing Campaign Management, HubSpot, Salesforce, Vendor Coordination
Serbia · Remote OK
Position Summary: The Safety Specialist II is an integral part of the safety team at Precision and performs all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR) for clinical …
Skills: ICSR Processing, Argus Safety Database, MedDRA, WHODrug, FDA Safety Regulations
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Lead the operational delivery of clinical trials, overseeing CRAs and managing all clinical aspects across multiple countries. Ensure timeline adherence, quality delivery, and effective communication between the sponsor and functional team members.
Requires a bachelor's degree in a science or health-related field and significant experience leading oncology clinical trials within a CRO, Pharma, or Biotech environment. Must have strong knowledge of GCP/ICH guidelines and the ability to travel internationally.
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Hungary, Poland, Romania, Serbia or Slovakia.
Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.
You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.
We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.
Minimum Required:
Other Required:
Skills:
Competencies:
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
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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
