Trial Activation Specialist

4 weeks ago


Beijing, Beijing, China Thermo Fisher Scientific Full time
Job Summary

We are seeking a highly skilled and detail-oriented Trial Activation Specialist to join our team at Thermo Fisher Scientific. As a key member of our clinical trial activation team, you will be responsible for preparing, reviewing, and coordinating country submissions in line with our global submission strategy.

Key Responsibilities
  • Prepare, review, and coordinate local EC submissions in alignment with our global submission strategy.
  • Support the preparation of local Moho submissions, as applicable, in alignment with our global submission strategy.
  • Coordinate with internal functional departments to ensure site start-up activities are aligned with submissions activities and mutually agreed-upon timelines.
  • Achieve PPD's target cycle times for site activation.
  • May have contact with investigators for submission-related activities.
  • May act as a key-contact at the country level for either Ethical or Regulatory submission-related activities.
  • Work with the start-up CRA(s) to prepare regulatory compliance review packages, as applicable.
  • Assist in developing country-specific Patient Information Sheet/Informed Consent form documents.
  • Assist with grant budgets and payment schedules negotiations with sites.
  • Enter and maintain trial status information relating to SIA activities onto PPD or client databases in an accurate and timely manner.
  • Ensure local country study files and filing processes are prepared, set up, and maintained as per PPD WPDs or applicable client SOPs.
Requirements
  • Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
  • Effective oral and written communication skills.
  • Excellent interpersonal skills.
  • Strong attention to detail and quality of documentation.
  • Good negotiation skills.
  • Good digital literacy and the ability to learn appropriate software.
  • Good English language and grammar skills.
  • Basic medical/therapeutic area and medical terminology knowledge.
  • Ability to work in a team environment or independently, under direction, as required.
  • Basic organizational and planning skills.
  • Basic knowledge of all applicable regional/national country regulatory guidelines and EC regulations.
What We Offer

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds, and perspectives are valued.



  • Beijing, Beijing, China Thermo Fisher Scientific Full time

    Unlock Your Potential as a Trial Activation Approval Specialist IIAt Thermo Fisher Scientific, we're committed to empowering our customers to make the world a healthier, cleaner, and safer place. As a Trial Activation Approval Specialist II, you'll play a vital role in bringing our mission to life by ensuring the smooth execution of clinical trials.Key...


  • Beijing, Beijing, China Thermo Fisher Scientific Full time

    Support the Preparation and Coordination of Clinical TrialsAt Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Clinical Trials Specialist, you'll play a critical role in supporting the preparation and coordination of clinical trials, ensuring that our customers receive the highest...


  • Beijing, Beijing, China Novo Nordisk Full time

    Key ResponsibilitiesWe are seeking a skilled Clinical Trial Feasibility Specialist to join our team at Novo Nordisk. The successful candidate will be responsible for developing and executing the early planning and clinical trial feasibility strategy in China CDC.Deliver in-time and in-quality early planning and feasibility activities for portfolio and...


  • Beijing, Beijing, China Thermo Fisher Scientific Full time

    At Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Clinical Trials Specialist, you'll play a critical role in the management and preparation of Country Submissions in line with our global submission strategy.Key Responsibilities:Prepare, review, and coordinate local regulatory...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    As a leading global contract research organization, Fortrea is seeking a highly skilled Clinical Trials Operations Specialist to support our pharmaceutical, biotechnology, and medical device customers.Typical AccountabilitiesSchedule and manage clinical trials, ensuring compliance with regulatory requirements.Develop and implement efficient clinical trial...


  • Beijing, Beijing, China Thermo Fisher Scientific Full time

    Job SummaryAt Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Trial Activation Approval Specialist II, you'll play a critical role in managing and preparing local regulatory submissions in line with our global submission strategy.Key ResponsibilitiesPrepare, review, and coordinate...


  • Beijing, Beijing, China Parexel Full time

    Unlocking Excellence in Clinical TrialsAt Parexel, we're committed to delivering exceptional results in clinical trials. As a Risk Management Specialist - Clinical Trials, you'll play a vital role in ensuring the success of our studies.Key Responsibilities:Develop and implement risk assessment strategies for clinical trialsCollaborate with cross-functional...


  • Beijing, Beijing, China Thermo Fisher Scientific Full time

    At Thermo Fisher Scientific, we're committed to enabling our customers to make the world a healthier, cleaner, and safer place. As a Clinical Trials Specialist II, you'll play a critical role in bringing our mission to life by participating in the management and preparation of Country Submissions in line with our global submission strategy.Key...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Key ResponsibilitiesDevelop and execute the early planning and clinical trial feasibility strategy in China CDC, ensuring timely and high-quality delivery of portfolio and clinical trials in CKAD and RareD TA.Act as the primary point of contact for internal and external stakeholders on clinical trial early stage discussions and decisions in China...


  • Beijing, Beijing, China Novo Nordisk Full time

    Key ResponsibilitiesWe are seeking a highly skilled Feasibility Manager to join our team at Novo Nordisk. As a key member of our China CDC team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy.Develop and execute the early planning and clinical trial feasibility strategy in China CDC.Deliver...


  • Beijing, Beijing, China Novo Nordisk Full time

    Key ResponsibilitiesAs a key member of our team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy in China CDC. This will involve delivering in-time and in-quality early planning and feasibility activities for portfolio and clinical trials in CKAD and RareD TA.You will serve as the main point of...


  • Beijing, Beijing, China Novo Nordisk Full time

    Key ResponsibilitiesDevelop and execute the early planning and clinical trial feasibility strategy in China CDC, ensuring timely and high-quality delivery of portfolio and clinical trials in CKAD and RareD TA.Act as the primary point of contact for internal and external stakeholders on clinical trial early stage discussions and decisions in China...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Key ResponsibilitiesWe are seeking a highly skilled Feasibility Manager to join our team at Novo Nordisk A/S.Develop and execute the early planning and clinical trial feasibility strategy in China CDC, ensuring timely and high-quality delivery.Deliver in-time and in-quality early planning and feasibility activities for portfolio and clinical trials in CKAD...


  • Beijing, Beijing, China IQVIA Full time

    Job SummaryWe are seeking a highly skilled Clinical Research Site Activation Specialist to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for ensuring the successful activation of investigative sites for clinical trials.Key ResponsibilitiesServe as Single Point of Contact (SPOC) for investigative...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    Company Overview:SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch is a dynamic and innovative company that is revolutionizing the development process of clinical trials. Our commitment to delivering life-changing ideas and therapies to patients in need drives us to seek motivated problem-solvers and creative thinkers who...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Clinical Trials Administrator to join our team at BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd. As a Clinical Trials Administrator, you will play a critical role in the success of our clinical trials by providing administrative support to our project teams.Key...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    Job Summary: We are seeking a highly organized and detail-oriented Clinical Trials Administrator to join our team at BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd. The successful candidate will be responsible for providing administrative support to our clinical trials team, ensuring the smooth execution of studies and maintaining...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    Job Summary: We are seeking a highly organized and detail-oriented Clinical Trials Coordinator I to support the day-to-day operations of our clinical trials. The successful candidate will provide administrative support to the project team, ensuring timely and accurate completion of tasks.Key Responsibilities:Document and track study activities using relevant...


  • Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full time

    About UsBEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.Company OverviewWe provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and...


  • Beijing, Beijing, China SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch Full time

    As a prominent global contract research organization (CRO) dedicated to scientific excellence and extensive clinical development expertise, SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch offers pharmaceutical, biotechnology, and medical device clients a comprehensive array of clinical development, patient access, and...