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Clinical Trial Management Jobs in Philadelphia, Pennsylvania

Clinical Trial Manager Jobs
By EPM Scientific At Philadelphia, PA, United States
Minimum 3 years of CAR-T experience
Strong oral and written communication skills with ability to work with cross-functional teams
Formulate and execute operational strategies to achieve successful in-house implementation and oversight of clinical trials focused on CAR-T
Oversee all aspects of trial initiation procedures, working in coordination with other departments within Clinical Operations
Uphold adherence to regulatory requisites, encompassing ICH-GCP, FDA directives, and other pertinent regulations throughout every phase of the trial's lifecycle
A BA/BS in science related field
Clinical Trial Associate Jobs
By ICON Strategic Solutions At Philadelphia County, PA, United States
You are part of the vendor selection and management process where appropriate
You prepare and execute Statement of Work (SOW) with vendor for local drug management
University degree in Health Science, or a related field (an equivalent combination of education, training, and work experience may be considered)
You review, discuss, and communicate packaging and labelling requirements, as defined by the protocol, with vendors
Two years experience in Clinical Research or related industry
Strong social and interpersonal skills (written and oral). You will be confident speaking to Health Care Professionals.
Clinical Trial Coordinator Jobs
By BriaCell Therapeutics Corp. At Philadelphia, PA, United States

We seek a clinical trial coordinator who worked at a patient care level, to supervise sites remotely from the Sponsor's perspective.

Clinical Trial Assistant Jobs
By RemeGen Biosciences At Pennsylvania, United States
Assist with general response to patient enrollment inquiries and seek management support when needed.
Manage SVP and study team calendars and set up meetings.
Excellent written and verbal communication skills.
Strong attention to detail and problem-solving skills.
· 3+ years of experience in health care, biopharmaceutical experience is strongly preferred.
Assist the clinical development teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Manager Jobs
By Iovance Biotherapeutics, Inc. At United, PA, United States
Lead role in vendor identification/qualification/selection, systems set-up/management including EDC, IWRS, Central Laboratories, specialty services (ePRO, eDiary, etc.)
Demonstrated experience in management of CROs, in vendor selection
Required Education, Skills, And Knowledge
Risk management and mitigation including prioritization of competing tasks and issues to ensure program/study objectives are successfully accomplished.
Ability to critically review and supervise a multifunctional vendor groups including clinical operations, data management and biometrics
Effectively tracks and communicate program/study progress to Senior Management with ability to create and update detailed dashboards and trackers
Clinical Trial Assistant / Etmf (Electronic Trial Master File) Coordinator
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Knowledge of clinical research processes, regulatory requirements, and good clinical practice (GCP).
Familiarity with eTMF systems and other clinical trial management systems.
Liaise with project managers, clinical operations staff, and other relevant team members to facilitate document collection and retention.
Monitor the progress of clinical trials and report updates to the project manager or clinical team lead.
Previous experience in a similar role, preferably within a pharmaceutical or biotech environment.
Excellent organizational skills and attention to detail.
Trial Attorney Jobs
By The Law Offices of Frederic I. Weinberg & Associates, P.C. At Conshohocken, PA, United States

Creditor’s Rights firm seeks associate to handle all aspects of litigation in all court levels in PA and NJ. Must be licensed in PA and NJ. Candidate must have 1 to 2 years litigation experience. ...

Comparator Sourcing Specialist - Clinical Trial Supply
By Eurofins Lancaster Laboratories At Horsham, PA, United States
Good organizational and time management skills
Proven work experience, preferably in a GMP area
Proficiency in Microsoft Word, and experience with ERP preferable
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Acting as primary point of contact internally for comparator sourcing
Advises on appropriate sourcing strategy
Remote - Senior Clinical Trial Specialist
By Beacon Hill Staffing Group At United States
5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.
Must have the ability to build and maintain positive relationships with management and peers
Manage the collection, review and approval of regulatory documents from clinical sites
Manages and tracks study specific payments
Manage ancillary vendors, such as a specialty lab
Review site visit reports, under the direction of the Clinical Program Manager or designee
Clinical Trial Manager Jobs
By SciPro At South San Francisco, CA, United States
**This opportunity may have future direct management responsibilities.
Manage vendor operational meetings to ensure project goals and timelines are met.
Early phase and start up experience required.
Demonstrated experience in selecting, managing, overseeing, and successfully developing effective relationships with multiple vendors and CROs.
Prior experience working in a start-up environment is a highly desired.
Responsible for study start-up, including working with cross functional teams on startup, and with the CRO on site selection/activation
Clinical Trial Manager Jobs
By Verily At Boulder, CO, United States
Experience in study project management and prior management of contracted resources/CROs.
Experience in site monitoring, clinical quality compliance and international study management.
Deep knowledge of the range of tools used in the clinical study management space.
BA/BS/BScN degree in health or biologic science, or equivalent practical experience.
Master's degree in health or biologic science, or equivalent practical experience.
Advanced knowledge of Good Clinical Practices and current knowledge of FDA regulations for clinical trials.
Clinical Trial Manager Jobs
By Cpl Life Sciences At Ohio, United States
Minimum of 2 years of Clinical Trial Management experience within a CRO
Project Management experience desirable for Senior Clinical Trial Manager (Associate Director level)
Location: Hybrid - (Remote considered for 5+ years CTM experience with some in-person meeting requirements)
Are you an experienced Clinical Trial manager or Project manager?
Management of overall project timeline
Do you have previous Oncology, Rare Diseases or CNS experience?
Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Nurse Navigator
By The Leukemia & Lymphoma Society At Rye Brook, NY, United States
Use problem solving skills to help patients overcome obstacles to enrollment
Maintain/increase knowledge and understanding of hematologic cancers, blood and bone marrow transplant and psychosocial aspects of living with cancer
Outstanding critical thinking, problem-solving, and collaboration skills
Demonstrated commitment to independent learning and skill enhancement
Serve in consulting role to the Information Resource Center about clinical trials
Contribute to continual process improvement of clinical trial support procedures
Clinical Trial Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
Clinical Trial Nurse - Nyc, Ny
By IQVIA At , New York $67,000 - $83,200 a year
2+ years of peds experience
Recent experience in drawing blood
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
Clinical Trial Assistant - Oncology - Palo Alto, Ca
By ICON At , San Jose
Support clinical trial registration and disclosure on websites per applicable regulatory requirements
At least 1 year experience as a CTA, CRC, or other role in clinical trials.
Proven organizational and presentation skills
Ability to manage multiple tasks with meticulous attention to detail
Excellent written and verbal communication skills
Good knowledge of the ICH/GCP
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
Investigator – Trial Office (Manhattan)
By The Legal Aid Society At , New York, 10013 $53,098 - $76,051 a year
Prepare written summaries of investigation results via our case management system
Discover and manage physical and digital evidence (e.g., cellphones, surveillance video, social media, etc.)
Bachelor’s degree in criminal justice or in a related field or demonstrated work experience
Prior experience conducting investigations on criminal cases preferred, including investigative internships
Additional training/certifications relating to criminal investigations preferred
Good listening and questioning skills
Clinical Trial Coverage Analyst, Remote
By University of Maryland Medical System At Baltimore, MD, United States
Skill in cost/financial accounting and clinical trial management software.
IV. Knowledge, Skills, And Abilities
Bachelor’s degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field required.
Certification in Healthcare Research Compliance or Epic preferred.
Demonstrated skill tracking clinical and corporate contracts using electronic administration software such as Grant.gov, CICERO, OnCore, Epic, etc.
Creates coverage analysis grids and analyzes the performance of the actual coverage analysis.
Trial Attorney Jobs
By US Securities and Exchange Commission At , Los Angeles, 90071 $163,744 - $272,100 a year
If you are relying on your education to meet qualification requirements:
All qualification requirements must be met by the closing date of this announcement.
DRUG TESTING: This position may be subjected to drug testing requirements.
You will be evaluated for this job based on how well you meet the qualifications above.
CITIZENSHIP: This position is open to US Citizens.
You must possess a J.D. or LL.B Degree.
Director, Clinical Trial Recruitment
By Spectrum Science - a GHMC Company At New York City Metropolitan Area, United States
Meets deadlines, manages priorities and effectively communicates to team members, vendor partners and supervisors.
At least 5-7 years of clinical trial patient recruitment and retention experience working in a global clinical trial environment
Advanced knowledge of Microsoft Office (Outlook, PowerPoint, Word, etc.)
Excellent written and verbal communication skills; strong presentation skills
If you choose to go into an office, take advantage of the pre-tax transportation benefits.
If you choose to work from home, use the office equipment stipend.
Clinical Trial Intern - Dallas, Tx
By Medpace, Inc. At , Irving, 75038, Tx
Excellent organizational, communication, and prioritization skills;
Knowledge of Microsoft Office; and
Competitive compensation and benefits package
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
Perform administrative duties in conformity with company policies and procedures;

Do you want to make a difference in the lives of patients? Join our team as a Clinical Trial Manager and help us bring innovative treatments to the world!

Overview of Clinical Trial Management Clinical Trial Management is a specialized field of healthcare that involves the management of clinical trials. Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are also responsible for the development of protocols, the recruitment of participants, and the collection and analysis of data. Detailed Job Description of Clinical Trial Management Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are responsible for developing protocols, recruiting participants, and collecting and analyzing data. They must also ensure that all safety and ethical standards are met. Clinical Trial Managers must be able to effectively communicate with research teams, sponsors, and regulatory agencies. They must also be able to manage budgets and timelines. Clinical Trial Management Job Skills Required
• Knowledge of clinical trial regulations and standards
• Excellent communication and organizational skills
• Ability to manage budgets and timelines
• Ability to work independently and as part of a team
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
Clinical Trial Management Job Qualifications
• Bachelor’s degree in a related field
• Experience in clinical research or clinical trial management
• Certification in clinical trial management (preferred)
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Knowledge
• Knowledge of clinical trial regulations and standards
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Experience
• Experience in clinical research or clinical trial management
• Experience in budget and timeline management
• Experience in working with research teams, sponsors, and regulatory agencies
Clinical Trial Management Job Responsibilities
• Develop protocols for clinical trials
• Recruit participants for clinical trials
• Collect and analyze data from clinical trials
• Ensure that safety and ethical standards are met
• Manage budgets and timelines for clinical trials
• Communicate with research teams, sponsors, and regulatory agencies