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Edc Project Manager Jobs in Oklahoma (NOW HIRING)

... in CTMS, EDC, eTMF, and Microsoft Project or equivalent tools. Preferred Qualifications: Master's degree in a health-related field 10 years of experience with a proven track record of managing ...

... in CTMS, EDC, eTMF, and Microsoft Project or equivalent tools. Preferred Qualifications: Master's degree in a health-related field 10 years of experience with a proven track record of managing ...

... in CTMS, EDC, eTMF, and Microsoft Project or equivalent tools. Preferred Qualifications: Master's degree in a health-related field 10 years of experience with a proven track record of managing ...

Software Engineer

Oklahoma City, OK · On-site

$70 - $126/hr

The ideal candidate must be able to handle multiple mission critical IT projects from new ... Hands‑on experience constructing and managing automated CI/CD build pipelines using tools such as ...

Edc Project Manager information

What is an EDC project manager?

EDC Project Managers are professionals who oversee the planning, execution, and monitoring of projects related to Electronic Data Capture (EDC) systems, primarily within clinical research and pharmaceutical industries. They coordinate between cross-functional teams, manage timelines, ensure regulatory compliance, and address any issues that arise during the data collection process. Their goal is to ensure that EDC systems are implemented efficiently and effectively, supporting the overall success of clinical trials. EDC Project Managers also act as the main point of contact for sponsors and stakeholders, ensuring that project objectives and quality standards are met.

What are some common challenges faced by EDC project managers when implementing new electronic data capture systems?

EDC Project Managers often encounter challenges such as ensuring seamless integration of the new system with existing clinical trial workflows, managing diverse stakeholder expectations, and maintaining data quality throughout the study. They must also handle tight timelines and adapt quickly to regulatory changes or sponsor requirements. Effective communication with both technical teams and clinical staff is crucial to overcoming these obstacles and ensuring successful project delivery.

What are the key skills and qualifications needed to thrive as an EDC project manager, and why are they important?

To thrive as an EDC Project Manager, you need expertise in clinical data management, project coordination, and a solid understanding of Electronic Data Capture (EDC) systems, usually supported by a degree in life sciences or related fields. Familiarity with EDC platforms like Medidata Rave or Oracle InForm, along with certifications such as PMP or CDISC, is highly valuable. Strong organizational, problem-solving, and communication skills help you effectively lead cross-functional teams and manage client expectations. These competencies ensure successful EDC project delivery, regulatory compliance, and high-quality clinical trial data.

What is the difference between Edc Project Manager vs Electrical Project Manager?

AspectEdc Project ManagerElectrical Project Manager
CertificationsPMP, OSHA, EDC-specific trainingPMP, OSHA, Electrical licenses
Work EnvironmentEnergy, utility, and infrastructure projectsConstruction, industrial, and commercial electrical projects
Industry UsageCommon in energy distribution and utility sectorsCommon in construction and industrial sectors
Job FocusDistribution systems, substations, and energy deliveryBuilding wiring, electrical systems, and installations

The Edc Project Manager primarily oversees energy distribution and utility infrastructure projects, focusing on energy delivery systems. In contrast, the Electrical Project Manager handles a broader range of electrical construction projects, including commercial and industrial wiring. Both roles require similar certifications but differ in industry focus and project types.

Does Edc Project Manager offer remote work options?

The Edc Project Manager role may offer remote work options depending on the employer's policies. Many project management positions can be performed remotely, especially with skills in collaboration tools and virtual communication platforms. Candidates should verify specific job postings for remote work availability.

What are popular job titles related to Edc Project Manager jobs in Oklahoma?

For Edc Project Manager jobs in Oklahoma, the most frequently searched job titles are:

Infographic showing various Edc Project Manager job openings in Oklahoma as of June 2026, with employment types broken down into 73% Full Time, 23% Part Time, 2% Contract, and 2% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Assistant Director of Research Projects

LSU AgCenter

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago


Job description

All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through "My Draft Applications" located on your Candidate Home page.Job Posting Title:Assistant Director of Research ProjectsPosition Type:Professional / UnclassifiedDepartment:LSUAM ORED - Institute for Health & Performance of Champions (Neil Johannsen (00003874))Work Location:1250 H.P. Long Field HousePay Grade:ProfessionalJob Description:

The Assistant Director of Research Programs will oversee the full lifecycle of complex, multi-disciplinary clinical studies within the LSU System, collaborating with elite academic, medical, and athletic partners. The AD will lead project planning, regulatory compliance, budgeting, inventory purchasing and maintenance, and team coordination to ensure that studies are executed with precision and scientific rigor. The ideal candidate has a strong background in managing multi-disciplinary clinical trials and thrives in innovative, cross-functional environments.

Job Responsibilities:

Cross-Functional Team Leadership: Lead and coordinate cross-functional project teams (clinical operations, data management, biostats, safety, regulatory, medical writing). Facilitate cross-functional team meetings, ensure documentation of decisions and action items. Act as Project Manager/Director to direct reports. Serve as the primary institute contact for internal and external stakeholders, and compile necessary data from ORED and IHPC research teams to provide regular project updates to stakeholders (40%).

Clinical Trial Planning & Execution: Lead planning, initiation, and execution of clinical trials from study start-up through closeout. Develop detailed project timelines, milestones, and resource allocation plans. Oversee site feasibility, selection, initiation, monitoring, and closeout. Work with clinical monitors, sponsors, and study teams to ensure high-quality site engagement and performance (25%).

Compliance, Risk, and Quality Oversight: Ensure compliance with ICH-GCP, FDA/EMA regulations, and internal SOPs. Proactively identify risks and develop/implement mitigation strategies, and lead issue resolution efforts to minimize study disruption and escalation. Support audit and inspection readiness activities (20%).

Resource Oversight: Development of clinical trial budgets for funding submissions and ensure adherence to project scope, budget, and deliverables. Oversee the selection, management, and performance of equipment and supply acquisition, maintenance, CROs and other vendors (e.g., labs, imaging providers, study specific vendors), equpment. Review and approve third party invoices and ensure adherence to contractual terms. Interface with the finance office in the Office of Research to ensure that allocation of resources to research projects are within the institute scope of funding (10%).

Other duties as assigned (5%).

Minimum Qualifications:

Bachelor's degree in a health-related field

3 years of experience in clinical research with some supervisory and clinical project management experience including but not limited to clinical trial budgeting, protocol and consent development, regulatory submissions, study implementation, and oversight of data collection and quality assurance. Strong knowledge of ICH-GCP, FDA/EMA regulatory requirements and clinical trial methodology, proficient in CTMS, EDC, eTMF, and Microsoft Project or equivalent tools.

Preferred Qualifications:

Master's degree in a health-related field

10 years of experience with a proven track record of managing complex, multi-site and/or multi-disciplinary studies preferred and some experience managing vendors, collaborators, sites, and cross-functional teams preferred.

LSU values skills, experience, and expertise. Candidates who have relevant experience in key job responsibilities are encouraged to apply -- a degree is not required as long as the candidate meets the required years of experience in the job description.

Additional Job Description:Special Instructions:Please provide a cover letter, resume, and three (3) professional references including name, title, phone number, and e-mail address.
Please attach ALL required documents under the "Resume/CV" section of your application.
A copy of your transcript(s) may be attached to your application (if available). However, original transcripts are required before hiring.
Due to the nature of the position and/or position responsibilities, this position shall be subject to pre-employment screenings in accordance with University Policy as required and RS:17 screenings (https://www.legis.la.gov/legis/Law.aspx?p=y&d=1297548).
For questions or concerns about updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu.
For questions or concerns regarding the status of your application or salary ranges, please contact Neil Johannsen at njohan1@lsu.edu.

Skills Needed:

Preferred Skills:

Posting Date:June 26, 2026Closing Date (Open Until Filled if No Date Specified):October 14, 2026Additional Position Information:

Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.

Benefits - LSU offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!

Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.

Essential Position (Y/N):LSU is an Equal Opportunity Employer.

All candidates must have valid U.S. work authorization at the time of hire and maintain that valid work authorization throughout employment. Changes in laws, regulations, or government policies may impact the university's ability to employ individuals in certain positions.

HCM Contact Information:

For questions or concerns related to updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu. For questions or concerns regarding the status of your application or salary ranges, please contact the department using the information provided in the Special Instructions section of this job posting.