In-House Clinical Research Associate
$50k - $70kAlira Health
Are you being referred to one of our roles by a connection in Alira Health? Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary The In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel. KEY RESPONSIBILITIES Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, etc. Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs Responds to sites’ regulatory board requests for protocol and ICF clarification as needed Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews Analyzes site performance problems (protocol adherence) and identifies solutions; provides ongoing training for study sites Maintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requests Conducts remote review of data entered on electronic Case Report Forms (eCRFs) Works closely with field CRAs and data management to resolve queries on discrepant data Assists with efforts to recruit investigative sites to participate in clinical studies Complies with ICH GCP guidelines, FDA regulations, and company SOPs Participates in internal, client/sponsor, scientific, and other meetings as required Manages and resolves conflicting priorities to deliver on commitments Performs additional duties as assigned DESIRED QUALIFICATION & EXPERIENCE BS/BA from an undergraduate program or equivalent experience 1-2 years of experience in clinical research Permanent authorization to work in the U.S. Languages English TECHNICAL COMPETENCES & SOFT SKILLS Proven ability to be careful, thorough, and detail-oriented Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills Self-starter who thrives in a collaborative, yet less structured team environment Ability to problem-solve unstructured or ambiguous challenges Strong command of English, both written and verbal Excellent communication and interpersonal skills with customer service orientation Proficient with MS Office Suite, particularly Word and Excel Contract Type Regular Salary Range The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope. USD $50,000 - 70,000 Alira Health is a global advisory firm providing consulting and research and clinical development services whose mission is to humanize healthcare and life sciences, in partnership with patients, through innovative technologies and expert guidance. From development to medical care, we complement the expertise of our Pharma, Biotech, and MedTech clients with a full spectrum of services across their entire solutions lifecycle. With offices around the world, Alira Health provides a vibrant and creative environment with benefits that include professional development, global travel, flexible work programs and more. We welcome your passion and drive, talent and entrepreneurial spirit, sense of service and teamwork. We are an integrated team of over 800 scientists, strategists, economists, clinicians, and biostatisticians representing over 30 nationalities. This broad global perspective and cultural richness has a direct impact on providing innovative solutions for our clients that lead to higher standards of care and an improved patient experience. #J-18808-Ljbffr Alira Health
- ...new medicines to those who need them. Job Description As a Clinical Research Associate you will work on the frontline of communication with project... ...communication and management Be a point of contact for in-house support services and vendors Communicate with internal project...HouseWork visa
$115k - $140k
...will utilize your skills, knowledge, and clinical judgement to provide a high standard of care... ...emergency situations based upon clinical research standards. Responsibilities Responsible... ...of computer software developed both in-house and off-the-shelf. Light to moderate lifting...HouseWork at officeLocal areaRemote workNight shift$100k
...protection is maintained, Good Clinical Practice (GCP), and... ...proficiency. Understanding of clinical research processes and regulations.... ...Society of Clinical Research Associates (SoCRA) or Association of Clinical... ...: Up to 20% travel for In-House Clinical Research Associates;...HouseContract workInterim roleLocal areaRemote work$85k - $130k
...important member of the Alira Health Clinical team. The CRA is highly motivated and... ...works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical Monitoring and... ...KNOWLEDGE AND LANGUAGES Knowledge of clinical research, ICH GCP and local regulations...HouseContract workInterim roleLocal areaRemote workFlexible hours- Cabaletta Bio is seeking a Senior In-House CRA to oversee monitoring of clinical trials, coordinate with sites, CROs, and vendors, and ensure inspection... ...friendly role reports to the Senior Clinical Trial Manager/Associate Director Clinical Operations and requires strong GCP,...HouseRemote job
$70 - $75 per hour
Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region (ideally based out of Boston, MA or Philadelphia, PA... ...visits according to established processes. Collaborate with in-house teams to ensure complete and timely submission of study...HouseHourly payContract workPart timeLocal areaRemote work$110.52k - $138.15k
...Oncology ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ..., or medicine. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and...Work experience placementFlexible hours- ...IQVIA is seeking a Clinical Research Associate to ensure smooth operation of study sites and drive breakthrough research in oncology. You will perform site visits, assist with recruitment plans, provide protocol training, and maintain TMF/ISF documents while ensuring regulatory...
- ...Clinical Research AssociateTo be eligible for this position, you must reside in the same country where the job is located. 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...Local area
- ...Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect...Work at officeRemote workFlexible hours2 days per week
- ...AbbVie is seeking a Clinical Research professional to advance clinical trials by engaging investigators, training site staff, and monitoring site performance with a strong focus on data integrity and patient safety. You will partner with sites to ensure compliant trial...
$92.32k - $126.94k
...that drive clear economic value, better clinical outcomes and improved quality of life for... ...CRA supports the day to day operations associated with the execution of clinical trials. He... ...of operational aspects of clinical research and regulatory regulations; Good interpersonal...Temporary workWork experience placementInterim roleWorldwide- ...SUMMARY: Under direction of the Manager of Grants & Special Projects, the Clinical Research Associate coordinates all aspects of clinical trials within the assigned unit.at the Adult Immunology Clinic, Highland Campus. In consultation with providers and other clinical...Full time
- ...Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to... ...PSI is the right place for you. Job Description As a Lead Clinical Research Associate, you'll provide leadership, oversight, and mentorship...Contract workRemote workWorldwideWork visa
- ...abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance...Contract workTemporary workLocal area
- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$90k - $110k
Avania is hiring Clinical Research Associates II (CRA II) - Medical Device Clinical Trials Salary range $90,000 - $110,000 + Annual performance related bonus + Benefits - Minimum 2+ years of prior CRA experience needed Avania's Clinical Research Associate II (CRA II)...- Clinical Research Assoicate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster... ...field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations...Flexible hours
- Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, ensuring compliance with the trial protocol and GCP. The role is remote with travel across the United States, coordinating between sponsors and sites to maintain trial...Remote job
- Elanco seeks a Senior Clinical Research Associate (CRA) - Animal Health to lead and execute monitoring for farm and companion animal studies within the Global Clinical Development Sciences team, ensuring studies meet GCP/VICH standards and support regulatory approvals....
- Syneos Health is seeking a Clinical Research Associate - Full-Service to support remote monitoring of site activities across the United States. You will conduct site qualification, initiation, interim monitoring, and close-out visits, ensuring compliance with ICH-GCP and...Remote jobInterim role
- Abbott Laboratories in Alameda, California is seeking a Clinical Research Associate I to support clinical trials, monitor site activities, and ensure protocol compliance under supervision. You will collaborate with cross-functional teams, assist with data collection and...
- ...office. QT Imaging is a medical device company engaged in research, development, and commercialization of innovative body imaging... ...QT Imaging is seeking a motivated and detail-oriented Clinical Research Associate (CRA) to support the execution and management of clinical...Contract workPart timeInterim roleWork at officeRemote work
- JOB DESCRIPTION: Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company...Worldwide
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
$130k
Avania is hiring SeniorClinical Research Associate (Sr CRA) Salary Range up to $130,000 + Annual Performance related bonus + Benefits Avania's ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical...- The Department of Digestive Diseases at UCLA is seeking a Staff Research Associate to support clinical studies in general gastroenterology, GI hemorrhage, and digestive diseases. You will collect and manage research data, maintain study databases, prepare reports, and...
$83.48k - $125.22k
About Karius Karius is a life science, venture-backed clinical metagenomics company, focused on elevating patient care through microbial... ...of education and experience. Three to five years of clinical research monitoring experience, including independent site management responsibilities...Interim roleWork at officeLocal areaRemote work- Location Portola Valley, San Mateo County Posted Aug 2026 About this position Position: Clinical Research Associate (CRA) Location: Redwood City, CA Length: 6 Month Contract Job Description: Were seeking a Clinical Research Associate (CRA) with strong clinical monitoring...Contract workInterim role
- Alameda Health System seeks a Clinical Research Associate to coordinate all aspects of clinical trials at the Adult Immunology Clinic, Highland Campus. Under the Manager of Grants & Special Projects, you will select, implement and monitor trials, educate staff and enroll...
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