Current jobs related to Senior Clinical Research Associate - Oslo, Oslo County - Optimapharm


  • Oslo, Oslo County, Norway TN Norway Full time

    Job OverviewClinical Research Associates are essential to the success of our clinical trials. As a key member of our team, you will be responsible for monitoring trial sites, ensuring compliance with regulatory requirements, and maintaining accurate records.We are seeking an experienced Clinical Research Associate to join our team in Norway. If you have a...


  • Oslo, Oslo County, Norway beBee Careers Full time

    **Job Description:**We are seeking an experienced Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing routine site visits, managing assigned sites, and ensuring site compliance.Responsibilities:Perform routine site visits independently, including pre-study, initiation, interim monitoring and...


  • Oslo, Oslo County, Norway IQVIA Argentina Full time

    Job OverviewWe are seeking an experienced Clinical Study Associate Lead to join our team at IQVIA Argentina. As a Clinical Study Associate Lead, you will be responsible for leading a team of clinical research associates and managing the overall conduct of clinical studies.The ideal candidate will have at least 3 years of experience in clinical research and a...


  • Oslo, Oslo County, Norway Clinical effectiveness research group Full time

    About the position:We are seeking a talented post-doc to join our world-leading Clinical Effectiveness Research group. The successful candidate will be responsible for further strengthening our innovative and dynamic environment.The group has extensive experience in conducting large trials and observational studies in clinical medicine, cancer screening, and...


  • Oslo, Oslo County, Norway Optimapharm Full time

    Clinical Research Associate (m/f/d) - NorwayLocation: home-basedWho we are? Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to deliver new therapies to improve and save patients' lives. Optimapharm's key priorities are our people and consistently exceeding our client's expectations.With 26 strategically located...


  • Oslo, Oslo County, Norway TN Norway Full time

    Job OverviewAbout TN NorwayTN Norway is seeking a highly skilled Clinical Research Associate to join our team. As a CRA, you will be responsible for ensuring the proper conduct of clinical trials at study sites.Essential FunctionsPerform site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on...


  • Oslo, Oslo County, Norway TN Norway Full time

    Social network you want to login/join with:Clinical Research Associate (m/f/d) - Norway, OsloClient:Location:Oslo, NorwayJob Category:OtherJob Reference:23076343de88Job Views:2Posted:16.04.2025Expiry Date:31.05.2025Job Description:Location: home-basedWho we are?Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to...


  • Oslo, Oslo County, Norway Clinical effectiveness research group Full time

    Join us in the Clinical Effectiveness Research group as a post-doc in Clinical trials and Clinical Epidemiology!Our team is dedicated to advancing knowledge in clinical medicine, cancer screening, and clinical epidemiology. We have extensive experience in conducting large trials and observational studies with over 300,000 patients. Collaborations with top...


  • Oslo, Oslo County, Norway beBee Careers Full time

    Job Description:We are seeking an experienced Clinical Research Associate to support our team in Norway. The ideal candidate will have a strong background in clinical trial monitoring and a high level of knowledge of ICH GCP Guidelines.Responsibilities:Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout...


  • Oslo, Oslo County, Norway Clinical effectiveness research group Full time

    About the position:A 100% post-doc position is available for MD's or PhD's in biomedical data science or biostatistics.The Clinical Effectiveness Research group is a world-leading research group with expertise in clinical and epidemiological research. We run large trials and observational studies in clinical medicine, cancer screening, and clinical...

Senior Clinical Research Associate

1 month ago


Oslo, Oslo County, Norway Optimapharm Full time

Location: home-based

Who we are?

Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to deliver new therapies to improve and save patients' lives. Optimapharm's key priorities are our people and consistently exceeding our client's expectations.

With 26 strategically located offices, Optimapharm operates in 40+ countries, giving unrivaled access to Patients and Investigators in all countries in Europe and North America.

In-depth expertise and long-standing experience, combined with a flexible and collaborative approach, allow optimization of design and planning; through its strong track record of delivery excellence and committed and stable project teams, Optimapharm has secured a high level of repeat business over the years.

We are looking for an experiencedClinical Research Associateto join ourClinical Operations teamin Norwayand support us in making a tangible difference to project sponsors and benefiting patients and their families all around the world.

What do we offer?
  • Working in a successful company that's growing and developing every day
  • Working with a highly experienced team of clinical research professionals
  • International projects andprofessional growth
  • Performance & referral bonuses
  • Employee engagement programs
  • Well-being initiatives
  • Training and development program
Who are we looking for? Qualifications andExperience
  • University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
  • At least3-4yearsof independent clinical trial monitoring experience
  • High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
  • Fluent in local language and English, both, written and spoken
  • Computer proficiency is mandatory
  • Ability to read, analyze, and interpret common scientific and technical journals
  • Excellent verbal and written communication skills
  • Very good interpersonal and negotiation skills
  • Ability to work independently, pro-active
  • Affinity to work effectively and efficiently in a matrix environment
  • A current, valid driver's license
Yourresponsibilities
  • Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits
  • Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
  • Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable
  • Identifying and escalating potential risks and identifying retraining opportunities for site personnel
  • Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution
  • Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor
  • Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable
  • Administration of site payments in accordance with relevant project instructions

By joining our growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.

If you would be interested in joining the Optimapharm team, please send your CV in English and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.

#J-18808-Ljbffr