Rvp, Sales - Trial Landscape
By H1 At , Remote $190,000 - $210,000 a year
Manage all sales team members and processes for high volume net new sales processes with large Pharmaceutical organizations.
10+ years of B2B SaaS experience, 3+ in a high growth startup environment
3+ years experience managing direct reports in SaaS
If you have experience selling to Feasibility, Clinical or Study Start Up teams within Life Science organizations, that’s a plus
Experience managing both net new business & renewals
Set sales goals and quotas
Trial Coordinator (Us) Jobs
By Lindus Health At United States
Strong communication skills and ability to deal with extensive participant interaction
Experience and understanding of research and clinical trials (ICH/GCP trained)
1+ years' experience working on clinical trials
Interacting with participants to make sure they have a great trial experience!
Employee benefits program including free Netflix and Spotify
Able to adapt and learn to use new technology to change the way research is delivered
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
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.
Sr. Clinical Trial Associate
By Randstad USA At New Jersey, United States
Update the clinical trial management system (CTMS) for assigned trials with updates working with the trial manager.
Manage internal study meetings inclusive of setting agendas, recording and distributing minutes.
4+ years of clinical trial experience, with 2+ years of industry experience supporting clinical studies at a CRO or pharmaceutical company
1+ years of experience working directly for a sponsor is also preferred
Excellent written and verbal communication skills.
Support the clinical operations team with all aspects from study start-up, maintenance and close-out.
Clinical Trial Associate Jobs
By Skills Alliance At United States
• Excellent communication, time management and organizational skills
• Work with the clinical operations team to prepare metrics and updates for management
• 2+ years of experience in a clinical operations role in the biopharmaceutical industry
• Experience planning and tracking deliverables and timelines
• Take ownership of assigned responsibilities, with guidance
• Specific experience in Lymphoma or CAR T trials
Trial Success Associate Jobs
By OneStudyTeam At United States
Knowledge or experience within clinical research is a plus, but not required
Experience working in customer service/success and/or in a client facing role.
Excellent communication (written and verbal) and collaboration skills.
2+ years of work experience that would support your success in this role.
Training CRAs or other sponsor users on the StudyTeam platform
Identifying opportunities to improve your and the team’s work
Clinical Trial Associate Jobs
By Summit Therapeutics, Inc. At Menlo Park, CA, United States
Experience, Education And Specialized Knowledge And Skills
Responsible for data entry and status updates within the Ipsen Clinical Trial Management System (CTMS)
Ability to work in a strong regulated environment within a quality management system (QMS)
Manage the clinical study creation and set-up for the country and site binders and the trial milestones.
Experience in clinical study environment within CRO or Pharmaceutical company.
Minimum: Knowledge of the clinical study environment with a strong theorical or practical administrative organization.
Clinical Trial Supply Associate
By Mindlance At United States
· SAP software based computer systems experience.
· MS Office and MS Teams experience.
·SKYPE Meeting or Virtual Meeting software experience.
·GMP and Pharmaceutical Industry Regulations knowledge.
Job Title:Clinical Trial Supply Chain Specialist
·Additional services provided include Product Complaint evaluation, classification, and notification, temperature excursion evaluation and processing.
Clinical Trial Management Associate
By Ionis Pharmaceuticals, Inc. At Carlsbad, CA, United States
Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and distributes management reports from internal tracking systems at requested intervals
Assists with the tracking and management of study specific budgets
Assists with facilitating resolution of data queries and requests from Clinical Data Management
Critically evaluates job tasks and the impact on overall trial management objectives
Collaborates with the Clinical Trial Manager and/or the Clinical Project Lead on the development of certain study-specific plans and/or processes
Prepares investigational site reference materials (i.e., screening/enrollment logs, Delegation of Site Responsibilities form, Site Monitoring Log, etc.)
Trial Clerk Jobs
By USAJOBS At Washington, DC, United States
Special Rating Factors (Knowledge, Skills, and Abilities Required by the Position):
Those who are required must abide by Selective Service registration requirements.
Trial Clerks Are Responsible For Providing Judicial Support Including
Taking notes of proceedings, notices, and rulings to prepare Court orders and minutes.
Responding to procedural questions from litigants, pro bono counsel, and the public.
Working closely with the Court's Docket Section to process exhibits, minutes, transcripts, orders, decisions, and other official case documents.
Clinical Trial Associate - (Malvern, Pa)
By KPS Life At Malvern, PA, United States
A working knowledge of clinical drug development and clinical operations processes and experience applying GCP, ICH and FDA requirements.
Complete any other task as assigned by direct manager.
Strong communication and organizational skills.
At least 3 years of experience pharmaceutical industry or clinical research site-based experience.
Knowledge of Regulatory and ICH GCP guidelines.
System experience preferably in CTMS, eDC, (e)TMF applications.
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. ...

Clinical Trial Associate (Cta)
By EPM Scientific At San Francisco Bay Area, United States
· Competitive salary with benefits
· Support US Post-marketing Global Registry and clinical trials activities
· Bachelor degree in Biological Sciences, Nursing, Pharmacy, or related major is preferred
· Understanding of ICH-GCP Guidelines
· High degree of commercial exposure early in your career
· Being a part of team whose work directly aims to improve the quality of people’s lives
Trial Attorney Jobs
By Lasater & Martin, P.C. At Greenwood Village, CO, United States

Lasater & Martin, P.C., a mid-sized national law firm, is expanding and looking to hire attorneys in our Colorado, Greenwood Village office.This office has a busy civil litigation defense ...

Regional Clinical Trial Associate
By DOCS At All, MO, United States
Lab ranges, supporting CRA in range collection and uploading
CTMS updates (site accounts, site contacts, milestones, site ICFs), supporting CRA and SSUs
ICF- customization per site, eTMF upload country and site ICF
Help with revision of documents to be submitted (SSU)
Ad hoc printing and shipping documents to sites
Organizing meeting and taking minutes, when required
Clinical Trial Associate Jobs
By Actalent At San Diego Metropolitan Area, United States
Inform the Clinical Operations Manager/Project Team on any outstanding document(s).
Support the Clinical Operations Manager(s) coordinating project meetings, including scheduling and drafting, distribution, and filing of meeting agendas and minutes.
Experience in managing eTMF platforms in an outsourced environment is required, with a minimum of 2 years of experience strongly preferred.
Understanding and working knowledge of regulations and standards applied in clinical areas, medical devices, and/or pharmaceutical products is required.
Strong skills with Microsoft Excel and SharePoint are required.
Communicate effectively with clinical study administration vendors (Functional Service providers etc.).
Trial Attorney Jobs
By Chaos Talent At Sandy Springs, GA, United States
Speaking ability to influence and expert-level legal writing and research skills.
Draft legal documents and perform legal research.
Provide ongoing communication and legal expertise to clients and pre-trial assist attorneys
Attend depositions, mediations, hearings, and court appearances
An active member in good standing with the state within which you currently are licensed and reside.
Recognized as “One of the Most Influential Law Firms in America” according to Trial Magazine.
Clinical Trial Associate Jobs
By AOA Dx At Boulder, CO, United States
·Bachelor’s degree (BS/BA) or equivalent combination of education and work experience in science related field
·Familiarity with document filing/management in an electronic Trial Master File preferred
·Manage spreadsheet and input payment terms and amounts for each clinical study/site
·1-2 years Clinical Operations or clinical research-related experience is preferred
·Excellent problem-solving, critical thinking, verbal, and written communication skills
·Ability to manage confidential information with discretion
Clinical Trial Associate Jobs
By NuWest Group At United States
• Excellent communication, time management and organizational skills
• Work with the clinical operations team to prepare metrics and updates for management
• 2+ years of experience in a clinical operations role in the biopharmaceutical industry
• Experience planning and tracking deliverables and timelines
• Take ownership of assigned responsibilities, with guidance
• Specific experience in Lymphoma or CAR T trials