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Edc Project Manager Jobs in Alabama (NOW HIRING)

Elevator Technician

Mobile, AL · On-site

$45 - $50/hr

Ability to manage installation projects and complete in a timely manner * High attention to detail ... Our Emergency Dispatch Center (EDC) provides 24/7/365 service to help dispatch local emergency ...

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 Alabama?

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

What cities in Alabama are hiring for Edc Project Manager jobs?

Cities in Alabama with the most Edc Project Manager job openings:

Hybrid Certified Registered Nurse Practitioner / CRC

Thermo Fisher Scientific

Birmingham, AL • On-site

Full-time

Posted 7 days ago


Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

174th of 544 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
The Hybrid CRNP/Clinical Research Coordinator is responsible for providing direct patient care as an Advanced Practice Provider while coordinating and managing clinical research studies in accordance with protocol requirements, Good Clinical Practice (GCP) guidelines, sponsor expectations, and regulatory requirements. This role bridges clinical care and research operations to ensure high-quality patient outcomes, protocol compliance, and successful study execution.
Essential Duties and Responsibilities
Clinical Practice Responsibilities (50%)
  • Conduct comprehensive patient assessments, including medical histories and physical examinations.
  • Diagnose and manage acute and chronic medical conditions within the CRNP scope of practice.
  • Develop and implement treatment plans.
  • Order, interpret, and review diagnostic tests and laboratory results.
  • Prescribe medications and therapeutic interventions in accordance with state regulations and collaborating physician agreements.
  • Provide patient education regarding disease management, medications, wellness, and preventive healthcare.
  • Document patient encounters accurately and timely in the electronic medical record (EMR).
  • Collaborate with physicians, nurses, and other healthcare professionals to deliver coordinated care.
  • Participate in quality improvement initiatives and patient safety activities.
Clinical Research Responsibilities (50%)
  • Serve as primary coordinator for clinical trials from study startup through closeout.
  • Screen, recruit, and enroll eligible research participants.
  • Conduct informed consent discussions and ensure proper documentation.
  • Schedule and coordinate protocol-required study visits.
  • Collect, review, and document study-related clinical data.
  • Process and ship laboratory specimens according to protocol requirements.
  • Maintain source documentation and regulatory binders.
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA requirements, and institutional policies.
  • Report adverse events, protocol deviations, and safety concerns promptly.
  • Coordinate monitoring visits, audits, and sponsor communications.
  • Assist Principal Investigators with study feasibility assessments and site selection activities.
  • Enter and reconcile data in electronic data capture (EDC) systems.
  • Track recruitment metrics and study performance indicators.
  • Support budget review and study startup processes as needed.
Qualifications
Required
  • Current Certified Registered Nurse Practitioner (CRNP) license in Alabama (or applicable state).
  • Master's or Doctoral degree in Nursing.
  • Current DEA registration and prescriptive authority.
  • Minimum 2 years of clinical practice experience.
  • Minimum 1 year of clinical research experience or equivalent research exposure.
  • Knowledge of GCP, FDA regulations, and human subject protection requirements.
  • Strong organizational and project management skills.
  • Proficiency with EMR and Microsoft Office applications.
  • Excellent communication and interpersonal skills.
Preferred
  • Certification as a Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP).
  • Experience in industry-sponsored clinical trials.
  • Therapeutic area experience in nephrology, oncology, cardiology, endocrinology, gastroenterology, or vaccines.
  • Experience with EDC systems such as Medidata Rave, Veeva, or Oracle Inform.
Competencies
  • Patient-centered care
  • Clinical judgment and decision-making
  • Attention to detail
  • Regulatory compliance
  • Time management
  • Leadership and collaboration
  • Problem-solving
  • Ability to manage multiple studies simultaneously
Physical Requirements
  • Ability to stand, walk, and sit for extended periods.
  • Ability to occasionally lift and move up to 25 pounds.
  • Dexterity required for clinical procedures, data entry, and specimen handling.
Work Environment
  • Hybrid role combining direct patient care and research operations.
  • Work performed in outpatient clinic and research settings.
  • Occasional travel for investigator meetings, training, or conferences may be required.
Reporting Structure
  • Reports to: Medical Director / Research Site Director
  • Collaborates with: Principal Investigators, Sub-Investigators, Clinical Research Associates, Research Staff, Medical Assistants, and Administrative Personnel

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