20 Best Clinical Research Associate jobs (Hiring Now!)

Senior Clinical Research Associate
Crinetics Pharmaceuticals —Remote
Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate…
$99,000 - $124,000 a year
Quick Apply
Clinical Research Coordinator
Mission Cancer + Blood —Des Moines, IA
Answer telephone, screen calls, take messages, and provide information to appropriate staff. Participate in presentations or seminars related to the field of…
Estimated: $46.2K - $58.5K a year
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3d
Clinical Research Associate/Senior Clinical Research Associate
Edgewise Therapeutics —Remote
The assigned clinical trials will be highly complex and high risk, e.g., multiple indications, data monitoring committees, interim analyses, adaptive design,…
$75,000 - $145,000 a year
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Clinical Research Associate
Katalyst Healthcares & Life Sciences —United States
Participating in regional and global conference calls and meetings to review progress of ongoing clinical trials. Familiarity with EDC systems (i.e. Oracle).
Estimated: $68.3K - $86.5K a year
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Clinical Research Associate
Sention Therapeutics, LLC. —San Diego, CA
The Clinical Research Associate is responsible for overall clinical site management, including site identification, feasibility, pre-study site evaluation,…
$140,000 - $190,000 a year
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Senior Clinical Research Associate I
Caidya —United States
Ability to drive an automobile and have a valid driver’s license, if applicable. Manages investigative sites in respect to the trial conduct and motivates sites…
Estimated: $92.8K - $117K a year
Clinical Research Coordinator, RN
Alliance for Multispecialty Research, LLC —Knoxville, TN
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$32 - $35 an hour
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Clinical Research Coordinator/Medical Assistant
Alliance for Multispecialty Research —Newton, KS
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
Up to $24 an hour
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1d
Research Budget & Contract Coordinator
Fort Wayne Medical Oncology & Hematology —Fort Wayne, IN
Works closely with Business Office, Pharmacist, hospitals and outside entities assuring budgetary compliance, invoicing, tracking payments and contract…
$22 - $25 an hour
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Clinical Research Assistant/Night Shift
Alliance for Multispecialty Research, LLC —Knoxville, TN
Assist in general office workflow which includes telephone answering. Answering and triage of research office calls. Experienced certified Medical Asst/EMT/LPN.
From $22 an hour
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Clinical Project Associate (REMOTE)
Fresenius Medical Care —Meriden, CT
Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
Estimated: $77.7K - $98.4K a year
3d
Senior Clinical Research Associate, Full Service
IQVIA —Remote
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
Estimated: $101K - $127K a year
6d
Clinical Research Coordinator
Essential Medical Research, LLC —Tulsa, OK
BS/BA in life sciences, biology, or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research…
$40,000 - $55,000 a year
Quick Apply
Principal Clinical Research Associate (Remote/Flexible)
Insulet Corporation —United States
Serves as initial point of escalation for sites and monitors/CRA and supports the monitoring of sites as needed with ability to manage complex studies and/or…
Clinical Research Associate I
Children's Minnesota —Minnesota
Assist research team with coordination and entry of research data. The department at Children's of Minnesota provides care for children of all ages with all…
$45,240 - $59,000 a year
Quick Apply
14d
Senior Clinical Research Associate
ProTrials Research, Inc. —United States
RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and…
$115,000 - $140,000 a year
3d
Clinical Research Assistant I - Infectious Diseases
The Henry M. Jackson Foundation for the Advancement of Military Medicine —Bethesda, MD
Preferred: Holds a valid driver’s license. Bachelor's Degree in Communications, Public Health, Life Sciences or a related field.
Estimated: $41.8K - $52.9K a year
16h
Clinical Research Coordinator/LPN
Alliance for Multispecialty Research, LLC —Norfolk, VA
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$24 - $27 an hour
Quick Apply
14d
In-house Clinical Research Associate
RHO —United States
Bachelors Degree in a life science, nursing or pharmacy field, along with at least 1 year of direct work experience managing essential documents within the CRO,…
$55,000 - $75,000 a year
9d
Clinical Research Contracts Associate
Dana-Farber Cancer Institute —Brookline, MA
Comprehension of science, research and translation of medical legal issues in clinical trials. Coordinates and holds independent meetings with industry partners…
Estimated: $80.8K - $102K a year
23h

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Senior Clinical Research Associate

Crinetics Pharmaceuticals - Remote

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Job Details

$99,000 - $124,000 a year

Benefits

Stock options
Employee stock purchase plan
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Biology
Management
Clinical research
5 years
Bachelor of Science
Writing skills
Bachelor's degree
Clinical trials
Good Clinical Practice
Documentation review
Communication skills
Negotiation

Full Job Description

Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world’s premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others.

Position Summary:

The Senior Clinical Research Associate (Sr. CRA) will participate in the preparation and execution of Phase 1-3 clinical trials. The Sr. CRA oversees the progress of clinical investigations by conducting site qualification, initiation, interim, and close-out visits. The Sr. CRA monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by Crinetics Pharmaceuticals and partner CRO(s). The Sr. CRA works closely with the Clinical Trial Manager (CTM) and Clinical Monitoring management to ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits, internal CRA training and evaluation visits, and CRO monitoring visit report review.

Essential Job Functions and Responsibilities:

These may include but are not limited to:

Develop strong, collaborative investigational site relationships and ensure continuity of relationships through all stages of the trial.
Perform clinical study site management/monitoring activities efficiently in compliance with GCP/ICH requirements, SOPs, local laws and regulations, protocol, Clinical Monitoring Plan, and associated documents.
Participate and provide input on site selection and site qualification activities.
Coordinate and manage assigned tasks in collaboration with the study team to achieve site activation.
Perform remote and on-site monitoring activities using various tools to ensure subject rights, safety and well-being are protected as well as the reliability and integrity of study data.
Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate visit reports and letters in a timely manner.
Review and verify study records including source documents, case report forms, informed consent forms and other materials to ensure data is complete and accurate.
Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain additional information on potential serious adverse events.
Assess and monitor investigational product receipt, storage, administration, accountability and return processes.
Collect, review, and monitor essential regulatory documentation maintained by the site for study start-up, study maintenance, and study close-out.
Submit site essential documents to the TMF following inline quality review and resolve any quality issues related to submitted documents.
Train and assist site coordinators, investigators, and CRO (as applicable) in collecting data and executing the study in a timely manner that meets the protocol requirements and timelines/milestones; serve as a resource to site coordinators, investigators and other staff members regarding investigational products and protocols.
Communicate and document contacts with investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, adverse event reporting, site audits/inspections, and overall site performance.
Identify, assess, and resolve site performance, quality or compliance problems and escalate as needed per defined escalation pathway in collaboration with CTM and/or Clinical Monitoring management.
Assist in the development and implementation of subject enrollment and recruitment strategies for site.
Manage and maintain visit information such as site/subject visit tracking and other documentation in Clinical Trial Management System (CTMS), Trial Master File (eTMF) and other systems.
Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, office and travel expense submissions and approvals as needed).
Ensure internal and study-related trainings are completed per study timelines.
Ensure all study deliverables are completed per Crinetics and study timelines.
Perform other Clinical Operations duties, as requested.

These activities may be performed by the Senior Clinical Research Associate depending on study assignment:

Review protocols, eCRFs, study manuals and other related documents, as requested by the CTM and Clinical Monitoring management.
Conduct CRA monitoring assessment visits, as needed.
Conduct co-monitoring, data collection visits with Crinetics or CRO CRAs, as needed.
Provide training/mentoring on operational tasks/projects to more junior staff.
Conduct monitoring oversight visits (MOVs) with CRO CRAs to assess compliance to the protocol and Clinical Monitoring Plan and document results of the visit.
Review monitoring visit reports from CRO and escalate monitoring trends or findings to the CTM and Clinical Monitoring management.

Education and Experience:

Required:

BS in biological sciences or related discipline with at least 5 years of experience in the role of Clinical Research Associate (an equivalent combination of experience and education may be considered).
Demonstrate an in-depth understanding of the study protocol and related procedures.
Demonstrate critical thinking, root cause analysis and problem solving to identify site process failures; develop corrective and preventative actions to bring sites into compliance.
Ability to motivate clinical site personnel to compliantly maintain/accelerate timelines to achieve clinical operational milestones.
An understanding and demonstrated application of Good Clinical Practices, ICH Guidelines and regulatory requirements. Able to comply with safety standards and respect privacy and confidentiality.
Excellent writing skills as they relate to the preparation of clinical trial documents.
Excellent interpersonal skills with strong oral/written communication and presentation skills.
Excellent negotiation skills and a tactful approach that leads to high value on services obtained and outcomes achieved.
Well versed with the latest trends in the clinical trial industry.

Preferred:

Monitoring experience in startup, execution and close out activities related to clinical studies; experience using risk-based monitoring processes preferred.

Physical Demands and Work Environment:

Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities.

Travel:

You may be required to travel for up to 75% of your time.

The Anticipated Base Salary Range: $99,000 - $124,000

In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience and education. Crinetics Pharmaceuticals is a multi-state employer, and this salary range may not reflect positions that work in other states. Your recruiter can share more about the specific salary range during the hiring process.

Equal Opportunity Employer:

Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender (including gender identity and/or expression), pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws.

Vaccination Requirement:

Following extensive monitoring, research, consideration of business implications, and advice from internal and external experts, Crinetics requires that all employees and contractors be fully vaccinated and have received the COVID-19 vaccines as a condition of employment. “Full vaccination” is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation.

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