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Clinical Project Manager
tech-res Bethesda, MD
$105k-134k (estimate)
Full Time | Scientific Services 6 Months Ago
Save

tech-res is Hiring a Clinical Project Manager Near Bethesda, MD

Job Title
Clinical Project Manager
Location
Bethesda, MD 20817 US (Primary)
Category
Clinical Operations
Job Type
Full-Time
Education
Bachelor's Degree
Travel
None
Job Description
  • Provide operational oversight of, and expertise to, cross-functional project teams, that will include task/functional managers who oversee the day-to-day operation for other functional areas.
  • Plan and manage day-to-day operational aspects of one or more assigned programs/projects or tasks, including the following, as required: planning/timelines, budgeting, resourcing, and vendor management/interfacing. Identify and proactively work to remove obstacles, mitigate risks, and escalates issues; both internally and to the client [Contracting Officers Representative (COR), or designee(s)], as needed.
  • Interface with clients and program/project staff; ensure provision of meeting agendas and summary documentation, as well as detailed information required for internal and client meetings.
  • Prepare and/or review full or sections for monthly, quarterly, and annual reports; may present at internal and/or scientific meetings.
  • Ensure documentation of processes and workflows are being followed and occurring within projected timelines and determine course of action to prevent and remediate delays. Identify gaps and propose solutions to improve efficiency and quality of deliverables. Maintain a high level of accuracy and attention to detail in a fast-paced environment with shifting priorities.
  • Carry out numerous and varied activities associated with the conduct and successful performance of clinical trials/studies with demonstrated expertise and ability to navigate in at least one project/contract-specific tool or system in support of the following: patient recruitment; data management, collection and processing of adverse events reports; tracking and reporting of site monitoring/management activities, and/or regulatory document collection (e.g., EDC, CTMS, or eTMF systems).
  • Represent clinical-trial related operations at study team meetings, participate in collaborative efforts and play an important cross-functional role.
  • Perform duties within established SOPs and in accordance with Good Clinical Practice (GCP). Ensure project quality and compliance with FDA regulations and ICH (R2) guideline, and with NIH policies or other sponsor-specific requirements.
  • Provide oversight and mentorship to staff in the delivery of quality work and performance metrics, as per task order and/or project deliverables.
  • Expect to include line management responsibility and staff hiring activities.
  • Support and comply with the company's Quality Management System policies and procedures. Drives innovative project and company performance improvement solutions, including corrective and preventive (CAPA) actions, as needed. Perform risk-based quality content reviews and monitor internal/external KPIs, as required by the client.
  • Contributes to Corporate Initiatives, e.g., SOP development and proposals for government and commercial clients.
Job Requirements
  • Working knowledge and application of FDA/EMA and other regulatory requirements, i.e., GCPs/ICH (R2) guidelines to include domestic and global regulatory requirements.
  • Broad multidisciplinary understanding of the pharmaceutical clinical research and development processes with hands on regulatory, clinical operations, or clinical trial monitoring/management experience, e.g., clinical study design, conduct, management, reporting, and/or product development life cycle.
  • Demonstrated ability to take a leadership role and drive quality progress.
  • Display excellent organizational skills and exhibit professionalism and integrity.
  • Demonstrated project and client management skills.
  • Strong presentation, problem-solving, and conflict resolution skills. 
  • Seasoned oral and written communication skills.
  • Expertise in Microsoft Word, PowerPoint, and Excel is required, and experience with Microsoft Project.
  • Background in Infectious Disease/HIV clinical trials and/or Oncology preferred; prior work on a government contract, is a plus.
We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Scientific Services

SALARY

$105k-134k (estimate)

POST DATE

11/21/2023

EXPIRATION DATE

06/20/2024

WEBSITE

tech-res.com

HEADQUARTERS

BETHESDA, MD

SIZE

100 - 200

FOUNDED

1979

TYPE

Private

CEO

NORA LEE

REVENUE

$10M - $50M

INDUSTRY

Scientific Services

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TRI provides product development support services to the global drug, biologic and medical device community.

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The job skills required for Clinical Project Manager include Planning, Leadership, Problem Solving, Initiative, Presentation, Written Communication, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Project Manager. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Project Manager. Select any job title you are interested in and start to search job requirements.

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The following is the career advancement route for Clinical Project Manager positions, which can be used as a reference in future career path planning. As a Clinical Project Manager, it can be promoted into senior positions as a Planner/Scheduler IV - Construction that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Project Manager. You can explore the career advancement for a Clinical Project Manager below and select your interested title to get hiring information.

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If you are interested in becoming a Clinical Project Manager, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Project Manager for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Clinical Project Manager job description and responsibilities

Clinical project managers collaborate with the other clinical trial team members to oversee work within the various phases.

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Clinical project managers lead many facets of the clinical trial process.

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Clinical project managers ensure research studies are successfully started and completed.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Clinical Project Manager jobs

Designate an experienced project manager.

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Communicate effectively with all project staff.

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Be willing to prioritize and negotiate project elements.

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Analyze progress and adjust project strategy.

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Build project management experience.

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Step 3: View the best colleges and universities for Clinical Project Manager.

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