Project Manager - RTSM
Posted 9 Mar 2022Confirmed open 47 min ago
Who can apply
United States only
Salary
$85K–150K
Per year, USD
Level
Lead / Staff
Full-time
Timezone
See description
About the role
The Role
Veeva Systems is looking for a Project Manager to join our Randomization & Trial Supply Management (RTSM) team. As a Project Manager, you will be the primary point of contact with the client including leading client meetings, training sessions, and highlighting the RTSM modules which will deliver an effective user-friendly RTSM system for end-users included in the study. Exceptional writing, editing/formatting, organization, and time management skills are a must.What You'll Do
- Review protocols and include required modules in the User Requirements Specification (URS)
- Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (included, but not limited to timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations and Clinical Trial Material Lists for assigned projects, User Acceptance Testing, and system set up)
- Ensure established timelines are met
- Facilitate and troubleshoot any issues associated with managing delivery of RTMS systems
- Provide technical advice and assistance to other project managers, developers, validation, and customer support staff
- Responsible for Tier 3 on-call coverage (24/7/365)
- Acquire new knowledge and enhance your skills
Requirements
- Four-year degree or equivalent experience
- Must have RTSM experience
- 2+ years of Project Management experience within the Clinical Trial Industry
- Ability to take initiative and work proactively
- Superior organizational and communication skills
- Working Knowledge Microsoft Office
- Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team
- A logical approach to problem-solving and excellent eye for detail
- Excellent verbal and written communication, interpersonal, and presentation skills
- Ability to travel (5-10%)
Nice to Have
- Working Knowledge of RTSM/IRT/IVRS/IWRS/IXRS
- Working Knowledge of FDA E6, E8, and 21 CFR Part 11
- Working Knowledge Subject Randomizations and Clinical Trial Material lists
- Audit Preparedness
- Google Docs
Interviewing with Veeva
- Follow the application process and submit your resume.
- Within 3 days, you will receive a link to a personality assessment administered by a third party.
- Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
- If moving to the interview stage, the process is as follows:
- A conversation with the hiring manager
- A practical case exercise
- A final conversation with our group's Senior Leader.
- Once all interviews are complete, the manager will be in touch with a final decision.
We value your time and believe in a transparent hiring process. Here is the process you can expect.
Perks & Benefits
- Medical, dental, vision, and basic life insurance
- Flexible PTO and company paid holidays
- Retirement programs
- 1% charitable giving program
Compensation
- Base pay: $85,000 - $150,000
- The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
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Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at [email protected].
Skills mentioned
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About Veeva Systems
Listing details & historyShowHide
- Employer posted
- 9 Mar 2022
- Last confirmed open
- 47 min ago
- Source
- Employer careers site
- Degree
- Degree or equivalent experience
- “What You'll Do Review protocols and include required modules in the User Requirements Specification (URS) Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (included, but not limited to timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations and Clinical Trial ”
- Visa
- Not stated
- Timezone
- What You'll Do Review protocols and include required modules in the User Requirements Specification (URS) Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (included, but not limited to timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations and Clinical Trial Material Lists for assigned projects, User Acceptance Testing, and system set up) Ensure established timelines are met Facilitate and troubleshoot any issues associated with managing delivery of RTMS systems Provide technical advice and assistance to other project managers, developers, validation, and customer support staff Responsible for Tier 3 on-call coverage (24/7/365) Acquire new knowledge and enhance your skills Requirements Four-year degree or equivalent experience Must have RTSM experience 2+ years of Project Management experience within the Clinical Trial Industry Ability to take initiative and work proactively Superior organizational and communication skills Working Knowledge Microsoft Office Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team A logical approach to problem-solving and excellent eye for detail Excellent verbal and written communication, interpersonal, and presentation skills Ability to travel (5-10%) Nice to Have Working Knowledge of RTSM/IRT/IVRS/IWRS/IXRS Working Knowledge of FDA E6, E8, and 21 CFR Part 11 Working Knowledge Subject Randomizations and Clinical Trial Material lists Audit Preparedness Google Docs Interviewing with Veeva We value your time and believe in a transparent hiring process.
- Languages
- Not stated
- Location evidence
- “Massachusetts - Boston”
Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.
History
- 18 Oct · Salary updated
- 18 Oct · source content changed
- 14 Oct · Salary updated
- 14 Oct · Location updated
- 14 Oct · eligibility changed
- 14 Oct · Description updated
- 14 Oct · Closing date updated
- 14 Oct · skills changed
- 9 Oct · Added to Remotavia