Praca Clinical Research Associate

Location: Poland Job Description: As a Clinical Research Associate, you will assume responsibilities encompassing various monitoring activities, contributing to clinical research across diverse therapeutic areas. Your role involves ensuring the adherence of clinical trials to the study protocol, ICH...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Regulatory Associate Consultant to join one of our clie...

IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and g...

Competitive Intelligence Associate page is loaded Competitive Intelligence Associate Bewerben locations Poland - Warsaw time type Vollzeit posted on Gestern ausgeschrieben job requisition id 4907411 Pfizer is continuously aiming to advance our business by delivering successful new medicines, forging...

I'm helping in the fight against cancer and beyond. And I do it I love to have brainstorming sessions when challenges come along, and we look for the best solution together as a team. Please introduce yourself and your role at Parexel. My name is Barbara Brzezińska. I am based in Poland and I work a...

Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with ...

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators...

Over one million people in the world today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many patients, the transplant itself can prove fatal or lead to serious conditions, such as graft versus host disease. Orca Bio's investigational, high...

Associate Market Access Specialist, Poznan page is loaded Associate Market Access Specialist, Poznan Apply locations Poznan, Poland time type Full time posted on Posted Yesterday job requisition id R1410754 Join the Angels Initiative Team today! Every 30 minutes a stroke patient who could have been ...

Primary Location Poland Job ID: PO_WA_CRA-0822 Job Type: Full-Time JOB DESCRIPTION Your main responsibilities: Perform site visits and monitoring activities in accordance with protocol, SOPs, GCP/ICH; Participate in study site selection, including on-site and remote (by phone) pre-study site evaluat...

Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do. Join ...

Overview Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, we’re committed to you ju...

Precision for Medicine is seeking an experienced Senior Clinical Data Associate to provide comprehensive data management support throughout all phases of the clinical trial data management process. Under direct supervision, you will ensure adherence to Standard Operating Procedures (SOPs), regulator...

Precision for Medicine is seeking an experienced Senior Clinical Data Associate to provide comprehensive data management support throughout all phases of the clinical trial data management process. Under direct supervision, you will ensure adherence to Standard Operating Procedures (SOPs), regulator...

Description of Services Co-ordinate/manage timely contributions of AZ core/extended members Interface with key stakeholders cross-functionally, and/or external partners, to identify, manage and resolve issues affecting study delivery Review protocol drafts and input operational perspectives/content ...