Research Coordinator

The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation created to enhance and expand the ability of the Alliance for Clinical Trials in Oncology (Alliance) to conduct cancer clinical research and address important treatment questions through large-scale clinical trials. Through efforts of the Foundation in support of the Alliance, clinical trials and laboratory research are conducted to discover new or improved ways to prevent, treat, and cure many types of cancer, including leukemia and lymphoma, and cancers of the breast, prostate, lung, and gastrointestinal (GI) tract, and help educate the medical community on methods of cancer diagnosis, treatment, and prevention.

The Foundation is looking for experienced laboratory science professionals transitioning into clinical research. This role will support the Translational Research Program (TRP) at the Alliance for Clinical Trials in Oncology and Alliance Foundation Trials (AFT). This role will serve...

Job Title: Clinical Research Coordinator (CRC)

Location: Bay Area, California

Employment Type: Full-Time, Permanent

Job Description

Stirling Q&R is seeking a dedicated and detail-oriented Clinical Research Coordinator on behalf of our confidential client. This role is based in the Bay Area and offers an exciting opportunity to manage and coordinate clinical research studies. The successful candidate will ensure compliance with regulatory standards while maintaining high-quality data collection and management.

Responsibilities

• Act as the primary contact for research participants, sponsors, and regulatory agencies.
• Screen, recruit, and obtain consent from study participants; review medical records and conduct interviews as needed.
• Schedule participant appointments and provide reminders or other necessary communications.
• Prepare and maintain...

The R&D Coordinator supports the Badger mission and principles through supporting the R&D department throughout the new product innovation process by researching, networking, managing documents, databases and laboratory resources. The R&D Coordinator plays a fundamental role in the full product development process from ideation to ingredient sourcing and formulation all the way through to scale up.

Essential Responsibilities:

Ingredient Sourcing:

·       Source new ingredients and back up ingredient suppliers in close coordination with the Production and Procurement Manager.

·       Vet new ingredients against mission-based standards and make recommendations for ingredient innovation.

·       Keep a record of the recommended new ingredients for each upcoming product development....

Cure HHT is a leading organization dedicated to advocating for patients and families affected by Hereditary Hemorrhagic Telangiectasia. We are seeking a passionate and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting ongoing and upcoming research initiatives aimed at improving the understanding, diagnosis, and treatment of HHT. This position will involve coordinating clinical studies, liaising with researchers and clinicians, managing data, and ensuring that our research efforts align with the organization's mission to advance patient care.

Key Responsibilities:

• Project Coordination:
• Help to coordinate and manage research projects, including clinical and observational studies.
• Develop and maintain project timelines, ensuring that all milestones are met according to schedule.
• Organize and facilitate meetings with research teams,...

Job Summary:

The OCOM Research Coordinator / Grants Manager will work as an assistant to the Research Director and assist with the daily operation of the OCOM research department and will provide hands-on support to OCOM faculty and student research projects and scholarly activity under the direction of the Research Director.

Duties/Responsibilities:

• Apply for Grants from various organizations including: NIH, AOA, Industry
• Assist faculty and students with manuscript submission to medical journals under the guidance of the Research Director
• Daily attention to list of ongoing manuscript submissions, and tracking progress.
• Maintain roster of faculty and student scholarly activity including published articles, book chapters, and abstracts; and research presented at national and regional meetings.
• Maintain roster of faculty research compliance with CITI training.
...

Northwest Clinical Trials is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. As a leading research organization in the pharmaceutical research industry, we are dedicated to improving patient care through clinical trials. In this role, you will have the opportunity to work on groundbreaking research projects and contribute to medical advancements. If you have a strong passion for healthcare, attention to detail, and excellent organizational skills, we want to hear from you!

As a Clinical Research Coordinator, you will be responsible for managing all aspects of clinical trials, from planning to execution. You will work closely with physicians, nurses, patients, and other research staff to ensure the smooth operation of trials and the collection of accurate data. Your exceptional communication skills will be essential as you will act as the point of contact for study participants, providing them with detailed information about the trials...

About IHTC

At the Indiana Hemophilia & Thrombosis Center (IHTC), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As Research Data Coordinator, you will be responsible for the timely and accurate entering of large amounts of data into multiple systems, training staff on data entry to maintain continuity, and analyzing data for inconsistencies prior to entry.

The Opportunity

• ATHN data entry and quality assurance report review and monitoring
• Participate in projects requiring data collection, entry and analysis as requested.
• Troubleshoot data entry and other technical issues with various staff members.
• Train staff on appropriate data entry methods to ensure...

About IHI

At Innovative Hematology, Inc. (IHI), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As Research Regulatory Coordinator, you will be responsible for initiating, coordinating, and leading all IRB and regulatory processes within the Research department. This role will also support the Research department in a variety of other capacities, including ongoing audit preparation and internal document creation and review as needed.

The Opportunity

• Maintain IRB Tracker for all research studies within department
• Prepare and process new submissions, amendments, continuing reviews, and study closures
• Develop and create patient-facing study documents that comply with the...

About IHTC

At the Indiana Hemophilia & Thrombosis Center (IHTC), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As a Research Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.

The Opportunity

• Participate in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
• Function as an integral part of the research and comprehensive care teams, working with colleagues to meet deadlines and maintain a flexible schedule based on the needs...

A multi-year Clinical Research Coordinator (CRC) position is available at our research site in Plano, TX with an initial focus on an active pulmonary study from a major pharmaceutical sponsor. Working independently under the Research Program Manager, the CRC will be responsible for carrying out clinical research studies, including but not limited to participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. The CRC must be able to work in a medical clinic setting supporting the principal investigator (PI) with protocol requirements, display a high degree of initiative, and have excellent interpersonal, organizational, and time management skills.

The company is hiring full-time and part-time positions.

Interested candidates should send a current resume and introductory cover letter to s.mcauley@empowerclinics.com

May perform some or all the...

Are you a driven and detail-oriented individual with a passion for clinical research? Look no further! EPW Curesearch LLC is seeking a Clinical Research Coordinator (CRC) to join our dedicated team in Los Angeles County, CA

In this multi-year position, you will have the opportunity to work on an active pulmonary study conducted by a major pharmaceutical sponsor. As a CRC, you will be responsible for various aspects of clinical research including participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. You will work closely with the Research Program Manager and support the principal investigator (PI) in meeting protocol requirements.

We are looking for someone who can thrive in a medical clinic setting, exhibit a high degree of initiative, and possess excellent interpersonal, organizational, and time management skills.

We are currently hiring for...

The Senior Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI and internal teams to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

The Senior Clinical Research Coordinator will coordinate all research-related activities, including the initial set-up of the study, study participant recruitment and retention, delivery of the intervention, data collection, entry, and quality control activities, protocol compliance and patient safety. He/She will also work on monitoring...

The Research Coordinator is an integral part of the Design and Analytics team that bolsters the efforts of our advisors in a wide array of situations and applications. The Research Coordinator will have the opportunity to be a part of a department whose capabilities become increasingly critical in how we do business. As Commercial Real Estate becomes increasingly driven by analytics, our clients continue to demand data driven recommendations from our brokerage team. It is the role of the research team not only to provide innovative data solutions to our clients, but to also provide interpretation of this data and how it impacts the Wisconsin market. The role is ever evolving and requires flexibility and adaptability to new and unique requirements.

Responsibilities

• Update internal databases including but not limited to tenants in the market, competitive sets and business park summaries, property stacking plans and development...

About IHTC

At the Indiana Hemophilia & Thrombosis Center (IHTC), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As a Research Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.

The Opportunity

• Participate in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
• Function as an integral part of the research and comprehensive care teams, working with colleagues to meet deadlines and maintain a flexible schedule based on the needs...

About IHTC

At the Indiana Hemophilia & Thrombosis Center (IHTC), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As a Research Coordinator (Nurse), you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.

The Opportunity

• Participate in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
• Function as an integral part of the research and comprehensive care teams, working with colleagues to meet deadlines and maintain a flexible schedule based on the...

The Position

We seek to fill a Research Nurse Coordinator role in the Chicago, IL area. The candidate will be responsible for the accurate completion of visit procedures and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants.

The position includes a generous salary and benefits. (This is not a remote position).

Research Nurse Coordinator responsibilities include:

• Ensuring the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, ICH/GCP guidelines, Institutional Review Board (IRB) approvals, and institutional policies and procedures.
• Performing medical tests, including, but not limited to, patient vital signs, EKGs, phlebotomy, and nursing assessments.
• Administering investigational medications including oral,...