Job Title: Senior Associate, Clinical Contracts and Budgets – Biotech- Remote (JP8914) Location: Thousand Oaks, CA. (Remote Work) Employment Type: Contract Business Unit: US GSO-SM Duration: 12 months with likely extensions Rate: $35-40/Hr Posting Date: 7/22/2021 3 Key Consulting i...
Open Systems is searching for multiple Senior Project Managers in the Neuroscience space for a remote contract with complete understanding of the Clinical Trial process who has run his/her own trials. Specific indications within the neuroscience field include Rare Disease, Gene Therapy, Sleep/Ps...
Description Position at Premier Research Premier Research helps highly innovative bio-pharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, ra...
Description: Providence St. Joseph Health is calling a Research Budget Analyst PSJH to work remotely within our footprint: AK, CA, MT, NV, OR, TX and/or WA. We are seeking a Research Budget Analyst PSJH who will be responsible for the timely and accurate preparation and maintenance of budget...
Clinical Research Associate - Evidence (Remote) Location: United States Requisition Number3581Employment Type:Regular We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who...
Submission for the position: (Sr) Project Manager - Ophthalmology - PH IIIb/IV Team - Remote - (Job Number: 178628)PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right ...
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting...
JOB DESCRIPTION Role : Prepares, coordinates, and facilitates responses for sponsor Requests for Proposals (RFPs) or Requests for Information (RFIs). Works with assigned operational departments and Business Development (BD) to create and articulate win strategies, key selling points, and execu...
Description At UPMC, we’re all here for the same reason — to make Life Changing Medicine happen. If you are looking to start your career in recruitment or human resources joining our team in this role might be the perfect fit for you. The Temporary Onboarding Associate will play a unique an...
*Description*Position at Premier ResearchPremier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases.We're looking for an exceptional* C* *linical...
*Clinical Trial Manager - Major Sponsor **Remote *Kelly is currently seeking a Local Clinical Trial Manager for a long-term engagement at one of our Global clients.This role is a full-time, offering our enhanced benefit package options. As a Kelly employee within this group, you will be eligible for...
Senior Clinical Research Associate At ICON, it's our people that set us apart. As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only...
Overview ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our pat...
Position Title: Associate Director, Clinical Operations Program Lead (COPL) Function: Global Development Office Department: Global Clinical Operations Reports To (Position Title): Director or Senior Director, Clinical Operations OBJECTIVES: Provide operational expertise and strategic input to t...
Job Description Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
Job DescriptionSUMMARYThe Project Director (PD) oversees and directs a portfolio or program of multiple clinical trials, in accordance with Ergomed or Sponsor Standard Operating Procedures (SOPs) as applicable, federal and local regulations, ICH-GCP guidelines, and contracted parameters. The PD mana...
Job Description New hires based in the US & Puerto Rico will be required to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption or accommodation to this vaccination requirement, subject to applicable law. Our Clinical Research and Pharma...
Job Description New hires based in the US & Puerto Rico will be required to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption or accommodation to this vaccination requirement, subject to applicable law. Our Clinical Research and Pharma...
Job Description New hires based in the US & Puerto Rico will be required to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption or accommodation to this vaccination requirement, subject to applicable law. Our Clinical and Pharmacovigilan...
Job Description New hires based in the US & Puerto Rico will be required to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption or accommodation to this vaccination requirement, subject to applicable law. Our Clinical and Pharmacovigilan...
Remote USA or Canada GENERAL Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client. Serve as client’s contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working rela...
The Project Manager of biometrics, you will be responsible for supporting the Biometrics team comprised of biostatistics, data management and statistical programming. You will be the owner of Biometrics timelines for upcoming regulatory submissions and ad-hoc requests needed for presentation outside...
Remote Clinical Research Associate Location Austin, TX Type Direct Hire Salary $1 - $2 / yr ID BN38-2698383 Posted Aug 18, 2021 Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitor...
Submission for the position: (Sr) Project Manager - Early Development Services Team (Phase I Trials) - US Remote - (Job Number: 187415)PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not onl...
Summarized Purpose: Responsible for the overall coordination and management of clinical trials from start up through to final deliverables. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials. Works with major functional area lea...
Job Description Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
Job Description Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
Salary: $85,000 - 100,000/yearThis position is fully remote, and requires candidates to be local to the Baltimore, MD, area for occasional on site meetings. About usWe are an award-winning managed IT service provider, delivering professional services expertise and Cloud, Security, and...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Summarized Purpose: Responsible for the overall coordination and management of clinical trials from start up through to final deliverables. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials. Works with major functional area lea...
Job Overview: Labcorp Drug Development has an exciting opportunity for an Associate Clinical Data Manager within the Clinical Data Management team. The Associate Clinical Data Manager can be remotely located anywhere within the United States. Collaborate and functionally report to Lead DM (LD...
Job Overview: Labcorp Drug Development has an exciting opportunity for an Associate Clinical Data Manager within the Clinical Data Management team. The Associate Clinical Data Manager can be remotely located anywhere within the United States or Canada. Collaborate and functionally report to Lead DM ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Companys clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
$1 to $2 Per Year Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progre...
Responsible for completing and coordinating in-house project activities associated with monitoring functions of Phase I-IV clinical research studies. Perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).Conduct ...
HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our beco...
HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our beco...