Senior Clinical Operations Lead - Sponsor Dedicated (m/w/d) job opportunity at IQVIA Holdings, Inc..

Home Jobs In United Kingdom Tag: Job Senior Clinical Operations Lead - Sponsor Dedicated (m/w/d) position at IQVIA Holdings, Inc.


DatePosted 5 Days Ago bot
IQVIA Holdings, Inc. Senior Clinical Operations Lead - Sponsor Dedicated (m/w/d)
Experience: 3-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeMaster's (M.A.)
loacation Reading, Berkshire, United Kingdom, United Kingdom
loacation Reading, Berks..........United Kingdom

The Senior Clinical Operations Lead will be responsible to support the Clinical Trial Manager/operational team in execution of the trial(s). The function could include direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. Maintain effective communication with project team through oral and written correspondence, status reports to ensure alignment with study timelines. Funtions: Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents. Create Master ICF template and review/approve site changes (in consultation with legal, safety when warranted). Update template for new risks and new amendments information. Participate in the feasibility and evaluation of investigative sites; working closing with the Clinical Trial Logistics group. Coordinate and monitor activities at investigational sites; review monitoring trip reports and support the US monitoring organization. Assist in the development and management of study timelines and priorities, including recruitment tools/strategy and patient retentions plan. Plan and organize meetings with team support (eg. investigator/coordinator meetings, DMC, SMC, safety call, etc.). Assist in the development of the IP and co-medication strategy (Quantities, labels, depots, tracking, etc.) working closely with other departments. Participate in data review and discrepancy resolution. Participate in coordinating efforts with internal Pharmacovigilance, and safety group. Monitor study-specific timelines and key deliverables; focus on management of all external vendors (e.g Monitoring, Sample management, IVRS, Laboratory, etc). Participate as a member of the multi-disciplinary trial(s) team. Develop relationships with investigational sites and institutions to enhance conduct of the trial. Acts as preliminary liaison for study sites to convey trial information, answer questions and in accordance with the escalation pathway. Assume responsibility to participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations Department. Qualifications: BS/BA degree or a relevant degree with strong emphasis on science. Minimum of 5years of experience in the biopharmaceutical industry or other relevant clinical research experience. Must have 3 years of experience as Global Project Manager Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health authority experience. Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously. Prior experience in assisting the conduct and management of multinational clinical trials is preferred. *Please note This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Other Ai Matches

Specialty Sales Representative, Specialty Medicines, Sweden Applicants are expected to have a solid experience in handling Specialty Medicines, Sweden related tasks
Analyst/Associate Consultant, Primary Intelligence Applicants are expected to have a solid experience in handling Primary Intelligence related tasks
Medical Science Liaison (DRC) Applicants are expected to have a solid experience in handling Job related tasks
Clinical Research Associate or SrCRA (m/f/d), Single Sponsor, home-based Switzerland Applicants are expected to have a solid experience in handling Single Sponsor, home-based Switzerland related tasks
Pharmaberater m/w/d Orphan Drugs, HKL/Kardiologie Applicants are expected to have a solid experience in handling HKL/Kardiologie related tasks
Medical Science Liaison Applicants are expected to have a solid experience in handling Job related tasks
MedTech Part Time Clinical Consultant – Sacramento, CA Applicants are expected to have a solid experience in handling CA related tasks
Pharmaberater m/w/d Immunologie Applicants are expected to have a solid experience in handling Job related tasks
Clinical Trial Educator Applicants are expected to have a solid experience in handling Job related tasks
MedTech - Per-diem RN Clinical Educator - West Coast Applicants are expected to have a solid experience in handling Job related tasks
Expert Detailing Representative - FSWA Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, Georgian into English Applicants are expected to have a solid experience in handling Georgian into English related tasks
HE/HTA (Assoc) Consultant - Sr Consultant, Real World Solutions Applicants are expected to have a solid experience in handling Real World Solutions related tasks
Business Development Manager - Pharma Applicants are expected to have a solid experience in handling Job related tasks
Systematic Literature Review Analyst/Consultant - Athens or Lisbon Applicants are expected to have a solid experience in handling Job related tasks
Senior Medical Data and Safety Review Physician Applicants are expected to have a solid experience in handling Job related tasks
Intern - IQVIA Applicants are expected to have a solid experience in handling Job related tasks
MedTech - Clinical Educator (RN/RRT) - Per-Diem - Florida Applicants are expected to have a solid experience in handling Job related tasks
Senior Consultant, Statistics & Psychometrics Applicants are expected to have a solid experience in handling Statistics & Psychometrics related tasks
Pharmaberater m/w/d Schmerz, Allergologie, HNO, Nahrungsergänzungsmittel Applicants are expected to have a solid experience in handling Allergologie, HNO, Nahrungsergänzungsmittel related tasks
Apotheken-Außendienst m/w/d 02 Schmerzmittel, inkl. Muskel- u. Gelenkschmerzmittel / OTC Applicants are expected to have a solid experience in handling inkl. Muskel- u. Gelenkschmerzmittel / OTC related tasks
Mobile Medical Assistant/Phlebotomist-Per Diem In-Home Services Applicants are expected to have a solid experience in handling Job related tasks
Assoc Stat Programmer Applicants are expected to have a solid experience in handling Job related tasks