20 Best Clinical Trial Administrator jobs (Hiring Now!)

Senior Clinical Trial Manager
BioPhase —San Diego, CA
Prepare/review site study documents (i.e., site-specific informed consent, study tools/worksheets, investigator contracts, and site payments).
$155,000 - $165,000 a year
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Clinical Trial Associate
Spectrum Staffing Services —Hopewell, NJ
Supports management and maintenance of filing systems for non-TMF documentation. The maintenance and management of assigned sites IRB initial submissions.
$70,000 a year
Clinical Trial Pharmacist
Re:Cognition Health —Chicago, IL
Essential to this endeavour is the requirement for all RCH staff to operate at the highest standards, adhering at all times to Re:Cognition Health’s own…
Estimated: $103K - $130K a year
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Clinical Trial Specialist
US Foot & Ankle Specialists —Cincinnati, OH
Bachelor’s degree in scientific or health related field. The CTS compiles and maintains project-specific status reports, interacts with the sponsor, study sites…
Estimated: $55.5K - $70.3K a year
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Clinical Trial Manager
Celldex Therapeutics, Inc. —New Haven, CT
For studies which are outsourced to CRO partners, management of CRO interactions, including sponsor oversight of relevant functional activities (e.g., study…
Estimated: $90.6K - $115K a year
Assistant Director – Pre-Award Clinical Trials (Vanderbilt Ingram Cancer Center)
Vanderbilt University Medical Center —Nashville, TN
Problem Solving/ Complexity of work: Integrate knowledge and in-depth analysis from several areas to resolve complex problems that are both technical and…
Clinical Trials Start-Up Officer
Re:Cognition Health —Fort Worth, TX
Bachelor’s Degree in a science, technical, health-related field. Responsible for the management of the Clinical trials pipeline tracker on a day-to-day basis,…
$55,000 - $65,000 a year
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Clinical Trials Research Nurse, Clinical Trials, FT,8A-4:30P
Baptist Health South Florida —Miami, FL
Experience with computer data entry and database management. Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts.
$39.80 - $52.93 an hour
Clinical Trial Contract Attorney (Fully Remote, Engagement)
Latitude —West Conshohocken, PA
Licensed to practice and in good standing in any state; Pennsylvania is a plus. Our own experience as practicing attorneys and our client relationships enable…
$150,000 - $190,000 a year
Clinical Trials Research Assistant
Palm Research Center —Las Vegas, NV
Seeking experienced, mature medical assistant for busy clinical trials site. Experience with GCP training, EDC, and understand how clinical trials work.
From $16 an hour
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Clinical Trial Budget Specialist
Technical Resources International, Inc. —Bethesda, MD
Develop and revise clinical trials budgets for industry sponsored clinical studies as per protocol and study timelines.
Estimated: $77.6K - $98.2K a year
Clinical Trial Administrator
PSI CRO —Durham, NC
Equivalency is defined as a minimum of 2 years’ experience in corporate or academic environment where administrative experience and technical skills have been…
Estimated: $65.7K - $83.2K a year
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Project Manager,Clinical Trial,Disclosure,Clinical Technical Document, Study Protocol Writing
Tellus Solutions —Remote
Bachelor's degree required, preferably in a health or biological science field. Exhibits a moderate level of technical competencies and requires a low level of…
$47.19 an hour
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9d
Clinical Trial Manager
Arcellx —Redwood City, CA
BA/BS in science-related field with 6+ years' relevant work experience. Oversees scope, quality, timelines, and budget with the internal functional leads, CRO,…
$160,000 - $175,000 a year
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Senior Clinical Trial Manager
Genmab —Princeton, NJ
Experience within the field of oncology and/or first in human trials is preferred. Ability to proactively identify risks, develop mitigations, & resolve issues.
Estimated: $131K - $166K a year
Clinical Research Specialist -Cancer Clinical Trials
Houston Methodist Academic Institute —Houston, TX
Bachelor's degree in health science-related field. The Academic Institute aligns our research and education initiatives in service to the clinical mission,…
Estimated: $64.4K - $81.6K a year
Clinical Trial Associate
Deciphera Pharmaceuticals —Waltham, MA
May develop and maintain study documents. We are seeking a Clinical Trial Associate (CTA) to assist and provide support to the members of the clinical…
Estimated: $63.8K - $80.8K a year
Quick Apply
9d
Clinical Trial Manager
Asklepios BioPharmaceutical —Remote
Manage the cross functional study management team and CRO/vendor(s) related to all aspects of clinical trial operations and continuously assess operational…
Estimated: $125K - $158K a year
11d
Clinical Trial Associate
Bristol-Myers Squibb —Princeton, NJ
For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf…
Estimated: $73.2K - $92.8K a year
Clinical Trial Administrator
Kerecis —Minneapolis, MN
Bachelor’s degree in science-related field preferred. Very good knowledge of the English language (enabling free verbal and written communication and…
Estimated: $66.8K - $84.5K a year
6d

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Senior Clinical Trial Manager

BioPhase - San Diego, CA

Quick Apply

Job Details

Full-time $155,000 - $165,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Management
Clinical research
Vendor management
5 years
Master's degree
Bachelor's degree
Data management
Immunology
Clinical trials
Oncology
Clinical trials management
FDA regulations

Full Job Description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Life Sciences community. We are currently looking for an ONSITE Sr. Clinical Trial Manager to work for a leading San Diego area biotech company.

*Must be local to San Diego, CA & can accommodate 4 days/ week onsite schedule

Key Responsibilities:

· Oversee the performance of CROs and third-party vendors, including co-monitoring, to ensure compliance with study protocol and in accordance with scope of work; identify areas of concern and escalate to Clinical Operations Managers.

· Perform initial review of CRO and other third-party study vendor invoices for correctness.

· Develop and maintain good working relationships with CRO, investigators and study staff.

· Perform clinical data review of data listings and summary tables, including query generation.

· Assist with third-party vendor training on protocols and practices. Coordinate the logistics of product readiness with sites and internally. Work cross-functionally with product manufacturing, QA and supply chain management, to coordinate site training, product delivery, supply management to ensure readiness and product availability prior to patient treatment.

· Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations and study-specific manuals and procedures.

· Ensure timely response to queries and monitoring discrepancies.

· Plan and conduct investigator meetings as directed.

· Manage the investigational product (IP) and non-IP study drug accountability and reconciliation process.

· Review and/or approve IP release packages.

· Review key study quality metrics (e.g. patient eligibility, primary endpoint data, etc.) and determine appropriate action in conjunction with study team.

· Prepare and/or review study-related documents (e.g., Monitoring Plan, Laboratory Manual, Patient Diary, Pharmacy Manual, CRF Completion Guidelines, etc.).

· Track and report on current progress of the study including site activation, patient enrollment, monitoring visits and data submission backlogs.

· Contribute to the preparation of clinical protocols, amendments, informed consent forms, study manuals and guides, electronic case report forms, and any other clinical research related documents.

· Participate in the planning of QA activities, coordinating the resolution of applicable audit findings.

· Ensure audit-ready condition of clinical trial documentation including central clinical files; review monitoring visit reports to ensure quality and resolution of site-related issues; coordinates and assist in the planning of regulatory or ethics committee activities, as appropriate.

· Prepare/review site study documents (i.e., site-specific informed consent, study tools/worksheets, investigator contracts, and site payments).

· Manage clinical monitoring activities (including approval of visit report templates, monitoring plan, etc.) ensuring compliance with ICH/GCP and applicable regulations, including the management through resolution (e.g. CAPA) of any site or study level issues, deviations, etc.

· Participate in the selection, training, and evaluation of study personnel (contract and internal) to ensure the efficient operation of the function.

· Collaborate with cross-functional teams (e.g. Medical Monitor, Regulatory Affairs, CRO, vendors and Investigators/site staff).

Education/Experience Requirements:

Bachelor’s in Life Sciences or equivalent. Graduate degree preferred.
Therapeutic experience in autoimmunity is strongly preferred.
Proven experience in early phase clinical trials.
Thorough knowledge of clinical research concepts, practices, FDA regulations and ICH guidelines regarding drug development and data management methods.
5 or more years' experience managing clinical trials as the sponsor is preferred; prior working experience at a site or in a CRO is a plus.
Strong site management and CRO management skills required.
Experience monitoring sites and conducting other site management activities.

*Travel requirement up to 30%

What we offer:

As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

· Full support and career-development resources to help you reach your potential

· A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

Apply now and let's make work better!

www.biophaseinc.com

Job Type: Full-time

Pay: $155,000.00 - $165,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Experience level:

5 years

Medical specialties:

Oncology

Schedule:

8 hour shift
Monday to Friday

Education:

Bachelor's (Required)

Ability to Commute:

San Diego, CA 92121 (Required)

Ability to Relocate:

San Diego, CA 92121: Relocate before starting work (Required)

Willingness to travel:

25% (Required)

Work Location: In person

Quick Apply

Clinical Trial Administrator jobs

Senior Clinical Trial Manager

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Clinical Trial Specialist

Clinical Trial Manager

Assistant Director – Pre-Award Clinical Trials (Vanderbilt Ingram Cancer Center)

Clinical Trials Start-Up Officer

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Clinical Trial Contract Attorney (Fully Remote, Engagement)

Clinical Trials Research Assistant

Clinical Trial Budget Specialist

Clinical Trial Administrator

Project Manager,Clinical Trial,Disclosure,Clinical Technical Document, Study Protocol Writing

Clinical Trial Manager

Senior Clinical Trial Manager

Clinical Research Specialist -Cancer Clinical Trials

Clinical Trial Associate

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