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Career area: Clinical trial management – EMBL Fellows' Career Service

EMBL Careers

A life science careers blog for early career researchers

This blog aims to inspire early career researchers exploring different career options. We provide interview-based profiles of life scientists working in diverse science-related careers and articles on a broad range of career-related topics, with new content added on a regular basis.

Career area: Clinical trial management

Clinical trials are a large-scale undertaking, and there is a range of roles that coordinate and oversee all aspects including site selection, communications with doctors, trial protocols, data management and analysis. The pharma sector,  contract research organizations and hospitals, often employ PhD-qualified life scientists for these positions.

Roles and responsibilities

The most common area for life scientists to work in is in a coordinating role where tasks may include a subset of the following activities:

  • Coordinating with the sites where the trial will take place (‘investigator sites’)
  • Supporting or leading the design, writing and review of the study protocol, case report forms etc
  • Ensuring that all ethical and regulatory aspects are considered, collecting relevant documentation, and preparing registration / approval of the trial
  • Coordinating all aspects of the trial – for example, delivery of the medicine, patient recruitment via doctors, and schedule for activities associated with the trial with the clinical staff (nurses, doctors) who complete these (pre-assessments, treatment, follow-up)
  • In some roles, answering patient questions
  • Monitoring the ongoing trial – ensuring all data for the trial is accurately recorded and patients are tracked; following up on any adverse events 
  • Preparing for and attending internal meetings /calls to review timelines, milestones, budget; preparing for and attending external meetings/calls with vendors, site liaisons, regulatory authorities etc
  • Working closely with other team-member e.g. the biostatisticians analysing the data and medical writers who will prepare the final documentation for regulatory submission / publication

These coordinating roles may involve work directly at the site of the trial, but there are also opportunities for home or office-based roles that involve coordinating clinical trials across multiple locations.

Additionally, there are other roles focused on the management and analysis of clinical trial data. This area can be particularly interesting for life-scientists with quantitative or computational backgrounds. Entry-level roles in the data management area generally involve working in electronic data systems to encapture and track data about each participant in the trial, and resolving queries and issues with the data. More senior roles might involve more strategic input on data strategy, data clean-up and analysis etc, as well as supervising more junior staff. 

Knowledge and skills

In our careers & skills survey, 7 clinical trial management professionals told us about the competencies they used most often. The most commonly selected competencies were:

  • Resilient problem-solving (selected by 86% of the respondents)
  • Teamwork (71%)
  • Effective communication (71%)
  • Organization (57%)
  • Developing & focusing on a clear vision (57%)

Career entry and progression

Entry-level roles include ‘clinical research assistants’ and traineeships. Direct entry to operational roles may be possible particularly at CROs (contract research organizations) – PhDs often enter as ‘clinical research associate’ (CRA) or ‘clinical research monitors’. Some additional training (e.g. online courses providing an overview of clinical research) will increase your chance of entry into an operational role rather than a traineeship. With experience, you will likely advance to more senior roles such as clinical project manager or clinical research coordinator.

Example job titles 

  • Clinical research associate / scientist 
  • Clinical investigator / researcher
  • Clinical Trial / Study Coordinator / Lead / Project Manager
  • Clinical research data specialist
  • Clinical data associate
  • Clinical data team lead
  • Clinical research data analyst
  • Biostatistician

Why consider this career area?

In our careers and skills survey, scientists working in clinical research told us that they appreciate that their work:

  • is intellectually stimulating
  • involves collaboration/ working in a team
  • provides opportunities for personal growth

Want to learn more?

Additional resources on this blog

Interview-based career profiles for this career area

Laura Cortesi, Senior Operational Study Manager
Barbara Tizzano, Clinical Trial Manager

Sources / further information

Data roles

Further internal resources

For EMBL fellows

Within EMBL, further internal resources (e.g. recorded career seminars) can be found on our career exploration intranet pages.

Informational interviews

For all career areas, we highly recommend first learning more about the careers using the resources above, then conducting informational interviews to gain further insights directly from former PhDs working in career areas that interest you.

Last update: November 2022

EU flag and text, co-funded by the European Union
The EMBL Fellows' Career Service incorporates the EMBL Interdisciplinary Postdoc (EIPOD) career development programme. EI3POD and EIPOD4 have received funding from the European Union’s Horizon 2020 research and innovation programme under Marie Skłodowska-Curie grant agreements 664726 (2015-2020) and 847543 (2019-present) respectively.
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