Clinical Research Associate II
Pfm
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 bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. We are now recruiting Clinical Research Associate II to join our team in the Netherlands. This is a remote based position with travel to sites for morning visits. We are looking for candidates in the Netherlands with biopharma monitoring experience. About you: You are calm, thoughtful, and responsive when things don’t go as planned. You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game. You find quick and creative ways of overcoming difficulties. You have an impeccable eye for detail. You identify potential study risks and propose solutions on how to mitigate them. You take responsibility in the quality and outcomes of your work. You are adept at handling conflict by using tried and true resolution strategies. How we will keep you busy and support your growth: You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.). Qualifications: Minimum Required: Life science degree and / or equivalent experience 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research. Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions) Other Required: Excellent communication and organizational skills are essential. A team player. Evidence of a client focused approach Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions) Fluency in English, Dutch French will be a plus oncology monitoring experience will be a plus Preferred: Study start up activities experience. Please apply in English. #LI-EK1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. 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 View email address on click.appcast.io. 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 View email address on click.appcast.io so we can investigate and take appropriate action. Candidates must be legally authorized to work in the country of employment without employer sponsorship. #J-18808-Ljbffr Pfm
- Job Title: Clinical Research Associate II (CRA II) Job Location: United States - Remote Job Overview: The Clinical Research Associate II (CRA II) is responsible for monitoring assigned investigational sites throughout the clinical trial lifecycle. The CRA II serves as...SuggestedInterim roleRemote work
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€47.8k - €63k per year
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II...Full timePart timeWork at officeLocal area- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities: Participate and...
$16.5 - $27.65 per hour
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Research Technician II, Department of Oral Biology Position Title: Research Technician II, Department of Oral Biology. A Research Technician... ...possible compensation at the time of posting, the role and associated responsibilities, and the experience, education, and training...$91.34k - $114.17k
Clinical Research Associate, Onc/Hem At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise... ...of treatments that benefit patients worldwide. As a CRA II at ICON, you will design and analyze clinical trials,...Worldwide- Experienced Clinical Research Associate | Regionally Aligned Across US Syneos Health® is a leading fully integrated biopharmaceutical solutions organization... ...training as required. For Real World Late Phase, the CRA II will use the business card title of Site Management...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
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...visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track... ...of independent on-site monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or similar setting. • Equivalent combination...Full timePart timeLocal areaImmediate startWorldwide$103k - $130k
...players in biopharma and translational research. We’re bringing the best minds together... ...it happen, from hospital labs to mobile clinics. By helping providers, patients, and families... ...possible.The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation...Hourly payFull timeContract workRemote workWork from homeWorldwideFlexible hoursNight shift$58.66k - $81.68k
...Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinical, Phase I through Phase IV, and post-marketing studies...TraineeshipLocal area$24 - $29 per hour
...Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the... ...the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative...Hourly payWork at officeFlexible hours- ...final disposition. Responsibilities include compiling, analyzing, redacting, and reproducing documents for discovery, filing, legal research, witness communication, and assisting ADAs in court and at trials. A NY driver’s license with at least two years of driving...Work at office
$25.84 - $34.94 per hour
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...patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists... ...to conduct innovative translational and clinical research that is driving a revolution in... ...an experienced Laboratory Technologist II to join our Main Hospital Rapid Results...Monday to FridayFlexible hoursShift workNight shift$150k - $180k
...Stifel Stifel strives for a culture that puts its clients and associates first: a culture where everyone belongs, everyone is welcome,... ..., modeling, and organizational support to the senior level Research Analysts. Has mastered the foundational skills required of an...Local areaFlexible hours
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