Sr. Clinical lead

IQVIA

Durham (NC)

On-site

USD 120,000 - 150,000

Full time

3 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Health insurance

Job summary

IQVIA in Durham, NC seeks a Senior Clinical Lead to drive clinical delivery on large, multi-regional trials. You will lead clinical teams, partner with Project Leaders, ensure regulatory compliance and timely study milestones, and contribute to risk management and study finances.

You will mentor junior staff, support bid defenses, and collaborate with cross-functional teams to deliver high-quality results in a fast-paced environment.

Qualifications

  • Bachelor's Degree in health care or other scientific discipline required.
  • Requires 7 years clinical research/monitoring experience or equivalent.
  • Knowledge of ICH/GCP regulatory requirements and SOPs.
  • Contains broad protocol and therapeutic knowledge.
  • Understanding of project finances and budgeting.
  • Strong English written and verbal communication skills.

Responsibilities

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements.
  • Accountable for meeting recruitment targets and recruitment strategies.
  • Develop and monitor risk mitigation plans for the project lifecycle.
  • Ensure quality delivery and monitor clinical quality issues.
  • Manage project finances including EAC and changes against baseline.
  • Lead the clinical team in large, global trials and coordinate stakeholders.
  • Collaborate with cross-functional teams and report to stakeholders.
  • Oversee resourcing, staffing plans and training for the clinical team.
  • Conduct regular team meetings and provide performance feedback.

Skills

Communication
Leadership
Problem solving
Organization
Time management
Collaboration

Education

Bachelor's Degree in health care or other scientific discipline

Tools

Microsoft Word
Excel
PowerPoint

Job description

Job Overview

Senior Clinical Leads are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Senior Clinical Lead is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operating Procedures) SOPs, policies and practices. Senior Clinical Leads ensure clinical delivery to customers by leading clinical teams and partnering with Project Leaders and other functional teams to ensure projects meet delivery requirements at all times.

Essential Functions
  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
  • Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
  • Contribute to the development of the project risk mitigation plan. Manage clinical risks through the project lifecycle.
  • Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
  • Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
  • Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
  • Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
  • Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
  • Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
  • Conduct regular team meetings and communicate appropriately to achieve objectives.
  • Support professional development by providing feedback to clinical team line managers on performance relative to project tasks to support professional development.
  • Adopt corporate initiatives and changes and serve as a change advocate when necessary.
  • May contribute to the development of the clinical delivery strategy for business proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
  • May mentor and coach new peers as they assimilate into this role.
  • May attend site visits as applicable in support of project delivery.
Qualifications
  • Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required
  • Requires 7 years clinical research/monitoring experience or equivalent combination of education, training and experience. Req
  • Requires consolidated knowledge of Project management practices and terminology. Req
  • Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.; Req
  • Requires broad protocol knowledge and therapeutic knowledge.; Req
  • Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates. Req
  • Requires understanding of project finances. Req
  • Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
  • Communication - Strong written and verbal communication skills including good command of English language.
  • Problem solving - Problem solving skills.
  • Organization - Planning, time management and prioritization skills.
  • Prioritization - Ability to handle conflicting priorities.
  • Quality - Attention to detail and accuracy in work.
  • Results-oriented approach to work delivery and output.
  • Leadership - Good influencing and negotiation skills. Good judgement and decision-making skills. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
  • IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint;
  • Collaboration - Ability to establish and
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Study Manager
Senior Clinical Study Manager

Integrated Resources Inc. • Woodcliff Lake (NJ)

On-site
USD 100,000 - 130,000
Clinical Team Lead
Clinical Team Lead

Fortrea • United States

Remote
USD 120,000 - 180,000
Clinical Research Manager III (Remote Position)
Clinical Research Manager III (Remote Position)

Artech Information System LLC • United States

Remote
USD 120,000 - 160,000
Clinical Program Manager
Clinical Program Manager

Integrated Resources Inc. • New Haven (CT)

On-site
USD 90,000 - 150,000
Senior Clinical Research Associate
Senior Clinical Research Associate

Katalyst CRO • United States

Hybrid
USD 90,000 - 120,000
Director Clinical Research
Director Clinical Research

Bracco Imaging S.p.A. • Princeton (NJ)

On-site
USD 180,000 - 240,000
Clinical Operations - Global Lead
Clinical Operations - Global Lead

Avant Health LLC • Bethesda (MD), Northern (KY)

Hybrid
USD 120,000 - 190,000
Senior Project Manager, Clinical Operations
Senior Project Manager, Clinical Operations

Enigma Search • South San Francisco (CA)

On-site
USD 140,000 - 200,000
Clinical Project Manager
Clinical Project Manager

Telix Pharmaceuticals Limited • United States

On-site
USD 70,000 - 110,000
Junior / Lower Mid-Level - Clinical Trial Manager
Junior / Lower Mid-Level - Clinical Trial Manager

Katalyst CRO • Boston (MA)

On-site
USD 120,000 - 180,000